Relevant bibliographies by topics / Decanol

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Academic literature on the topic 'Decanol'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Decanol"

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To Quynh, Cung Thi. "STUDY ON THE AROMA MODEL OF VIETNAMESE CORIANDER LEAVES (Polygonum odoratum)." Vietnam Journal of Science and Technology 54, no. 4A (2018): 73. http://dx.doi.org/10.15625/2525-2518/54/4a/11980.

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The volatiles present in fresh Vietnamese coriander (Polygonum odoratum) were isolated by solvent extraction and analyzed by GC analyses, aroma extract dilution analysis and omission test. The fresh herb was characterized as green, citrusy, pungent, and floral odors. The saturated aldehydes C10,C11, C12, hexanal and decanol were most likely the principal contributors to Vietnamese coriander's characteristic aroma. The aroma reconstitution was finally examined by sensory evaluation methods based on the 5 key odorants mentioned above. The results of the omission experiments confirmed that dodecanal, decanal, hexanal and undecanal have significant impacts on the odor of Vietnamese coriander, while decanol does not play an important role.
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RILEY, M. "Decomposition of decanol and decanal over Ni- and H-ZSM-5." Journal of Catalysis 103, no. 1 (1987): 87–94. http://dx.doi.org/10.1016/0021-9517(87)90095-9.

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Rong, Guo, Zhu Xia-Shi, and Yan Peng-Quan. "The Liquid Crystal Structure Between System SDS/Decanol/Glycerol and SDS/Decanol/Formamide." Acta Physico-Chimica Sinica 8, no. 05 (1992): 664–67. http://dx.doi.org/10.3866/pku.whxb19920517.

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Kwon, Kyungok, Dongwon Lee, Yusaku Iwata, and Hiroshi Koseki. "Flash points of n-decanol." Journal of Loss Prevention in the Process Industries 21, no. 4 (2008): 478–80. http://dx.doi.org/10.1016/j.jlp.2007.11.002.

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Ali, Abbas, Nurhayat Tabanca, Betul Demirci, et al. "Insecticidal and Biting Deterrent Activities of Magnolia grandiflora Essential Oils and Selected Pure Compounds against Aedes aegypti." Molecules 25, no. 6 (2020): 1359. http://dx.doi.org/10.3390/molecules25061359.

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In our natural products screening program for mosquitoes, we tested essential oils extracted from different plant parts of Magnolia grandiflora L. for their insecticidal and biting deterrent activities against Aedes aegypti. Biting deterrence of seeds essential oil with biting deterrence index value of 0.89 was similar to N,N-diethyl-3-methylbenzamide (DEET). All the other oils were active above the solvent control but the activity was significantly lower than DEET. Based on GC-MS analysis, three pure compounds that were only present in the essential oil of seed were further investigated to identify the compounds responsible for biting deterrent activity. 1-Decanol with PNB value of 0.8 was similar to DEET (PNB = 0.8), whereas 1-octanol with PNB value of 0.64 showed biting deterrence lower than 1-decanol and DEET. The activity of 1-heptanol with PNB value of 0.36 was similar to the negative control. Since 1-decanol, which was 3.3% of the seed essential oil, showed biting deterrence similar to DEET as a pure compound, this compound might be responsible for the activity of this oil. In in vitro A & K bioassay, 1-decanol with MED value of 6.25 showed higher repellency than DEET (MED = 12.5). Essential oils of immature and mature fruit showed high toxicity whereas leaf, flower, and seeds essential oils gave only 20%, 0%, and 50% mortality, respectively, at the highest dose of 125 ppm. 1-Decanol with LC50 of 4.8 ppm was the most toxic compound.
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Sun, Daolai, Takuya Misu, Yasuhiro Yamada, and Satoshi Sato. "Advantages of using Cu/SiO2 catalyst for vapor-phase dehydrogenation of 1-decanol into decanal." Applied Catalysis A: General 582 (July 2019): 117109. http://dx.doi.org/10.1016/j.apcata.2019.06.007.

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Neumann, Grit, Nadja Kabelitz, Andreas Zehnsdorf, et al. "Prediction of the Adaptability of Pseudomonas putida DOT-T1E to a Second Phase of a Solvent for Economically Sound Two-Phase Biotransformations." Applied and Environmental Microbiology 71, no. 11 (2005): 6606–12. http://dx.doi.org/10.1128/aem.71.11.6606-6612.2005.

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ABSTRACT The strain Pseudomonas putida DOT-T1E was tested for its ability to tolerate second phases of different alkanols for their use as solvents in two-liquid-phase biotransformations. Although 1-decanol showed an about 10-fold higher toxicity to the cells than 1-octanol, the cells were able to adapt completely to 1-decanol only and could not be adapted in order to grow stably in the presence of a second phase of 1-octanol. The main explanation for this observation can be seen in the higher water and membrane solubility of 1-octanol. The hydrophobicity (log P) of a substance correlates with a certain partitioning of that compound into the membrane. Combining the log P value with the water solubility, the maximum membrane concentration of a compound can be calculated. With this simple calculation, it is possible to predict the property of an organic chemical for its potential applicability as a solvent for two-liquid-phase biotransformations with solvent-tolerant P. putida strains. Only compounds that show a maximum membrane concentration of less than 400 mM, such as 1-decanol, seem to be tolerated by these bacterial strains when applied in supersaturating concentrations to the medium. Taking into consideration that a solvent for a two-liquid-phase system should possess partitioning properties for potential substrates and products of a fine chemical synthesis, it can be seen that 1-decanol is a suitable solvent for such biotransformation processes. This was also demonstrated in shake cultures, where increasing amounts of a second phase of 1-decanol led to bacteria tolerating higher concentrations of the model substrate 3-nitrotoluene. Transferring this example to a 5-liter-scale bioreactor with 10% (vol/vol) 1-decanol, the amount of 3-nitrotoluene tolerated by the cells is up to 200-fold higher than in pure aqueous medium. The system demonstrates the usefulness of two-phase biotransformations utilizing solvent-tolerant bacteria.
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Čejková, Jitka, František Štěpánek, and Martin M. Hanczyc. "Evaporation-Induced Pattern Formation of Decanol Droplets." Langmuir 32, no. 19 (2016): 4800–4805. http://dx.doi.org/10.1021/acs.langmuir.6b01062.

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Mao, X. H. "Stripping of titanium from TBP-decanol phase." IOP Conference Series: Materials Science and Engineering 164 (January 2017): 012029. http://dx.doi.org/10.1088/1757-899x/164/1/012029.

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Friberg, Stig E., Steven M. Jones, and C. C. Yang. "GELATION OF FORMAMIDE - CETYLTRIMETHYLAMMONIUM BROMIDE -DECANOL MICROEMOLSIONS." Journal of Dispersion Science and Technology 13, no. 1 (1992): 45–63. http://dx.doi.org/10.1080/01932699208943295.

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Dissertations / Theses on the topic "Decanol"

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Teixeira, Cilâine Verônica. "Estudo da Influência de Aditivos (Decanol e Anestésico Local Tetracaína) em Sistemas Micelares." Universidade de São Paulo, 1999. http://www.teses.usp.br/teses/disponiveis/43/43133/tde-15082012-152330/.

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Neste trabalho estudamos a influência que os aditivos decanol e o anestésico local tetracaína (TTC) exercem sobre a estrutura de sistemas micelares. Foram estudadas particularmente a influência do decanol na estrutra das micelas do surfactante aniônico dodecil sulfato de sódio (SLS) e da TTC na estrutura micelar do SLS e do surfactante zwiteriônico N-hexadecil-N, N-dimetil-3-amônio-1-propanosulfonato (HPS). O estudo de soluções micelares concentradas (razão molar água:SLS, Mw= 45,2) do sistema binário SLS/água e do sistema ternário SLS/decanol/água por difração de raios X nas vizinhanças das transições de fase isotrópica (I) SETA hexagonal (Halfa) líqüido-cristalina indicam que existe um empacotamento das micelas em uma ordem hexagonal local na fase I do sistema binário, e a fase Halfa tem empacotamento típico de objetos finitos/rígidos. No sistema ternário, em contraste, o empacotamento é relaxado através de um crescimento micelar induzido pelo decanol e a fase Halfa, que ocorre a uma concentração molar decanol:SLS, Md = 0,20, tem um comportamento típico de objetos infinitos/flexíveis. Uma seqüência intrigante de fases HalfaSETA nemática cilíndrica (Nc) a Md= 0,25 foi também investigada e é atribuída a um efeito combinado de crescimento micelar e mudança na rigidez da micela, com aumento da quantidade de decanol. O subseqüente aumento em Md leva o sistema à transição de fase Nc SETA nemática discótica (Nd) (Md= 0,38), acompanhada de uma mudança de forma micelar cilindro SETA disco. A influência do decanol em soluções isotrópicas mais diluídas (Mw= 144,0) foi estudada por espalhamento de raios X a baixos ângulos (SAXS) e analisada através das funções distribuição de distâncias p(r) e da distribuição de densidades eletrônicas rô(r). Os resultados mostram que micelas esferoidais crescem por influência do decanol e mudam de forma esferoide SETA cilindro a Md= 0,20 e cilindro SETA disco a Md APROXIMADAMENTE IGUAL A 0,40. Portanto, tornou-se evidente que a evolução de forma micelar do SLS pela influência do decanol é governada pela energia de curvatura da interface polar/apolar, uma vez que o decanol prefere localizar-se em interfaces planas, e que as transições de fase líqüido-cristalinas dependem dessas mudanças, associadas a efeitos de ordem estrutural em soluções concentradas. A influência da TTC em micelas aquosas de SLS e HPS foi estudada pelas técnicas espectroscópicas de fluorescência e ressonância paramagnética eletrônica (RPE) e por SAXS. Os resultados de fluorescência indicam que a droga é incorporada nas micelas, sendo que a TTC protonada se localiza mais próxima à interface polar/a polar das micelas, enquanto que a desprotonada penetra mais o interior hidrofóbico. Os resultados de RPE concordam com estas observações e indicam um aumento na organização molecular das micelas de SLS com a incorporação do anestésico local. Este aumento é mais pronunciado para micelas compostas por SLS e TTC carregada. Por outro lado, não foi observada nenhuma alteração significativa na organização molecular de micelas de HPS por influência da TTC. Através dos resultados de SAXS não foi observada nenhuma alteração na dimensão e na forma micelar por adição gradual de TTC neutra em SLS ou carregada em HPS, até a razão molar TTC:SLS, \'M IND. TTC\'= 0,30. Já os resultados de SAXS para os sistemas compostos por SLS e TTC protonada evidenciam um crescimento de micelas elipsoidais prolatas com anisometria v APROXIMADAMENTE IGUAL A 1,5 a \'M IND. TTC\'= 0 para v APROXIMADAMENTE IGUAL A 1,8 a \'M IND. TTC\'= 0,20 e 0,30. Os resultados são discutidos em termos de alteração das forças envolvidas na formação micelar (eletrostáticas e hidrofóbicas) e da própria estrutura molecular da TTC.<br>The influence of the aditives decanol and the local anaesthetic tetracaine on the micellar structure of the anionic surfactant sodium dodecyl sulfate (SLS) and zwiterionic N-hexadecyl-N, N-dymethyl-3-ammonio-1-propane-sulfonate (HPS) has been studied. The study of concentrated micellar solutions (water:SLS molar ratio, Mw= 45.2) of the binary system SLS/water and ternary SLS/water/decanol through X-ray diffraction dose to the liquid-crystalline isotropic (I) \'SETA\' hexagonal (Halfa) phase transition indicates a local micellar hexagonal packing in the I phase in the binary system, whereas the Halfa phase exhibits a packing typic of finite/rigid objects. On the other hand, the ternary system presents a more relaxed packing through a micellar growth induced by decanol, and the Halfa phase, which occurs at the decanol:SLS molar ratio, Md= 0.20 has got a typical infinite/flexible objects behaviour. An intriguing Halfa \'SETA\' cilindric nematic (Nc) phase sequence was also investigated at Md= 0.25 and has been atributed to the combined effect of the micellar growth and change of rigidity with the increasing in decanol amount. A further increase in Md leads to the Nc \'SETA\' discotic nematic (Nd) transition (Md= 0.38), which is accompanied by the cylinder \'SETA\' disc change of form. The infiuence of decanol in more diluted solutions of SLS/water (Mw= 144.0) has been studied through small-angle X-ray scattering (SAXS) and analysed through the distance distribution function p(r) and electronic density distribution rô(r). The results show that the spheroidal micelles grow due to the influence of decanol, changing from spheroid to cylinder form at Md= 0.20 and from cylinder to disc at Md= 0.40. Therefore, it became evident that the evolution of the SLS micellar shape under the effect of decanol is dominated by the bending curvature energy from the polar/apolar interface, since the decanol prefers the flat interfaces, and the liquid-crystalline phase transitions depend on these changes of shape, associated to structural order effects in concentrated solutions. The influence of TTC on SLS and HPS micelles were studied through fluorescence and electronic paramagnetic resonance espectroscopic techniques as well as by SAXS. The fluorescence results indicate that the drug incorporates into the micelles in such a way that the protonated TTC is localized close to the polar/apolar interface, whereas the uncharged form penetrates deeper into the hydrophobic core, in SLS micelles. The EPR results agree with the above observation besides indicating an increase in the SLS micellar molecular organization as the local anaesthetic is incorporated. Such an increase is more pronounced for micelles composed of SLS and charged TTC. On the other hand, no meaningful alteration in the HPS micelles molecular organization was observed under the TTC influence. From the SAXS results, we have not detected any changes in the micellar dimension and shape by gradual addition of either neutral TTC in SLS or charged TTC in HPS up to the TTC:SLS molar ratio (\'M IND. TTC\') of 0.30. Conversely, the SAXS results for systems composed of SLS and charged TTC have shown a micellar growth of prolate ellipsoidal micelles from anisometry v APROXIMADAMENTE IGUAL A 1.5 at \'M IND. TTC\'= O to v APROXIMADAMENTE IGUAL A 1.8 at \'M IND. TTC\'= 0.20 and 0.30. The results are discussed in the view of alterations in the forces involved in the micellar auto-assembling (electrostatic and hydrophobic) and the TTC structure.
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Viola, Dimas Henrique Lanfredi. "Estudo experimental e correlação da entalpia em excesso molar de soluções líquidas binárias contendo 1-nonanol ou 1-decanol e acetonitrila a diferentes temperaturas e pressão atmosférica utilizando os modelos ERAS e PFP." [s.n.], 2011. http://repositorio.unicamp.br/jspui/handle/REPOSIP/266896.

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Orientador: Artur Zaghini Francesconi<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia Química<br>Made available in DSpace on 2018-08-19T04:03:32Z (GMT). No. of bitstreams: 1 Viola_DimasHenriqueLanfredi_M.pdf: 2239811 bytes, checksum: 6bf0b52a70649c64b5b66555fd7154a6 (MD5) Previous issue date: 2011<br>Resumo: Neste trabalho foram obtidos dados experimentais da entalpia molar em excesso em função da composição das soluções líquidas binárias contendo 1-nonanol ou 1-decanol e acetonitrila a (298,15, 303,15 e 308,15) K e pressão atmosférica utilizando um calorímetro de solução Parr 1455 modificado. O modelo ERAS e a teoria PFP foram aplicados na tentativa de correlacionar os dados experimentais. Todas as soluções estudadas apresentaram valores positivos para a entalpia molar em excesso em todo o intervalo de composição. Os resultados de entalpia molar em excesso aumentam com o aumento da temperatura e do número de átomos de carbono do álcool. O modelo ERAS e a teoria PFP descrevem satisfatoriamente o comportamento da entalpia molar em excesso dos sistemas estudados<br>Abstract: In this work, experimental excess molar enthalpies ( ) of binary liquid mixtures containing 1-nonanol, or 1-decanol + acetonitrile have been determined as a function of composition at (298.15, 303.15 and 308.15) K and atmospheric pressure using a modified 1455 Parr solution calorimeter. The solution model ERAS and the PFP theory were applied with the attempt of correlating the experimental data. E m H All the studied systems showed values of excess molar enthalpy positive over the whole composition range. The results of excess molar enthalpy increase with the temperature and with the number of carbons in the alkanol chain. The solution model ERAS and the PFP theory were able to describe the main features the behavior of excess molar enthalpy for the studied systems<br>Mestrado<br>Sistemas de Processos Quimicos e Informatica<br>Mestre em Engenharia Química
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Zakri, Cécile. "Étude de la fusion-cristallisation de monocouches de 1-alcools à la surface de l'eau : mesures d'élasticité latérale par diffraction de rayons X et par une méthode mécanique." Université Joseph Fourier (Grenoble ; 1971-2015), 1997. http://www.theses.fr/1997GRE10107.

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Les proprietes elastiques et le scenario de fusion-cristallisation des 1-alcools courts, amphiphiles partiellement solubles dans l'eau, sont etudies. La monocouche est formee a partir d'une goutte d'alcool, deposee a la surface de l'eau et qui constitue un reservoir de matiere. En faisant varier la temperature, une transition est detectee par ellipsometrie et tension de surface. Par diffraction de rayons x sous incidence rasante, on sait qu'il s'agit d'une transition entre phase solide hexagonale rotateur et phase liquide. Cette fusion, nettement du premier ordre pour les alcools longs, semble changer de nature pour les chaines plus courtes. Par diffraction de rayons x sur un montage a tres haute resolution, une etude approfondie du scenario de fusion bidimensionnelle des chaines longues et de la monocouche de decanol est realisee. La constante elastique de cisaillement et la compressibilite sont extraites de l'analyse des formes de raies. Une experience mecanique de mesure de la constante elastique de cisaillement de films, concue entierement au laboratoire, est decrite. Elle apporte des informations complementaires sur la cinetique de cristallisation des monocouches de 1-alcools. Cette technique de mesure se revele surtout bien adaptee a l'etude de la cristallisation des proteines telles que la ctb. Elle permet une comparaison entre la cinetique d'adsorption, determinee par ellipsometrie et la cinetique de nucleation et croissance des cristaux de ctb en monocouche de lipides.
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Avendaño, Valdez Jorge. "Palabras del Decano." Pontificia Universidad Católica del Perú, 2015. http://repositorio.pucp.edu.pe/index/handle/123456789/115928.

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Cruchaga, Belaunde Miguel. "Encuentro con tu Decano." Universidad Peruana de Ciencias Aplicadas (UPC), 2021. http://hdl.handle.net/10757/655787.

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Bookhalter, Sharon R. "Requisites for effective decanal leadership." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0016/MQ47130.pdf.

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Mesquita, Francisca Maria Rodrigues. "Study of solvents alternative for aromatic extraction." Universidade Federal do CearÃ, 2015. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14637.

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CoordenaÃÃo de AperfeÃoamento de Pessoal de NÃvel Superior<br>Aromatic hydrocarbons are chemical compounds of great interest in the petrochemical industry. These are commonly derived from reformed naphtha, which are in multicomponent mixtures with aliphatic hydrocarbons. The separation of these components is realized, generally, the liquid-liquid extraction process. In this process, the sulfolane is the most widely used solvent. However, this has some disadvantages such as high cost. For this reason, many studies are developed by the academic community in order to propose alternative solvents to replace the exclusive use of sulfolane by compounds that are important features like good selectivity, easy recoverability and low costs. Given the above, this study main aims to determine liquid-liquid equilibrium data (LLE) to study the ability of solvents [diethylene glycol (DEG), triethylene glycol (TEG), glycerol and 2-hydroxyethyl amine format (2-HEAF)] in extracting aromatic mixtures with aliphatic. The physical properties also of great importance in the understanding of the behavior and interactions that occur in liquid mixtures. Thus, in this study were also studied the density and viscosity of solvent extractors aromatic. The experimental methodology for the determination of LLE data was initially validated by reproducing the literature, and the results showed good agreement between these data. After the method has been validated, solubility curves and tie-lines were constructed for systems containing decane + toluene + DEG (+ TEG, + glycerol, + 2-HEAF, + sulfolane) at T = (303.15 and 333.15) K. The composition data of tie-lines, obtained experimentally, were used to calculate the selectivity parameter and the distribution coefficient. With this data, it can be concluded that all the solvents studied have a good capacity for toluene extraction from mixtures with decane. However, the glycerol has presented as the most promising solvent for aromatics extraction. Finally, the experimental data were correlated through the thermodynamic activity coefficient models, NRTL and UNIQUAC. The results were considered satisfactory, noting that the NRTL was the model that presented minor deviations in compositions. Thus, best represented the LLE data for the systems studied.<br>Os hidrocarbonetos aromÃticos sÃo compostos quÃmicos de grande interesse na indÃstria petroquÃmica. Estes sÃo comumente originados da nafta reformada, onde encontram-se em misturas multicomponentes com hidrocarbonetos alifÃticos. A separaÃÃo destes componentes à realizada, em sua grande maioria, pelo processo de extraÃÃo lÃquido-lÃquido. Nesse processo, o sulfolano à o solvente mais utilizado. No entanto, este apresenta algumas desvantagens, tais como alto custo. Por esse motivo, inÃmeros estudos sÃo realizados pela comunidade acadÃmica a fim de propor solventes alternativos que substituam o uso exclusivo do sulfolano por compostos que tambÃm apresentem caracterÃsticas importantes, como boa seletividade, boa recuperabilidade e baixos custos. Diante do exposto, o presente trabalho tem como principal objetivo determinar dados de equilÃbrio lÃquido-lÃquido (ELL) para estudar a capacidade dos solventes [dietilenoglicol (DEG), trietilenoglicol (TEG), glicerina e 2-hidroxietilamina formato (2-HEAF)] em extrair aromÃticos das misturas com alifÃticos. As propriedades fÃsicas tambÃm assumem extrema importÃncia no conhecimento do comportamento e das interaÃÃes que ocorrem nas misturas de lÃquidos. Deste modo, neste trabalho foram estudados a densidade e a viscosidade de solventes extratores de aromÃticos. A metodologia experimental para obtenÃÃo dos dados de ELL foi inicialmente validada reproduzindo dados da literatura, e os resultados mostraram uma boa concordÃncia entre estes dados. ApÃs a metodologia ter sido validada foram construÃdas curvas de solubilidade e tie-lines para os sistemas contendo decano + tolueno + DEG (+ TEG, + glicerina, + 2-HEAF, + sulfolano) a T = (303,15 e 333,15) K. Os dados de composiÃÃo das tie-lines, obtidos experimentalmente, foram utilizados para calcular o parÃmetro de seletividade e o coeficiente de distribuiÃÃo. De posse desses dados, pode-se concluir que todos os solventes estudados apresentam boa capacidade para extraÃÃo de tolueno a partir de misturas com decano. No entanto, a glicerina destacou-se como o solvente mais promissor para a extraÃÃo de aromÃticos apresentando os maiores valores para seletividade. Finalmente, os dados experimentais foram correlacionados atravÃs dos modelos termodinÃmicos de coeficiente de atividade, NRTL e UNIQUAC. Os resultados foram considerados satisfatÃrios, observando-se que o NRTL foi o modelo que apresentou os menores desvios na composiÃÃo. Dessa forma, representou melhor os dados de ELL para os sistemas estudados.
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Dougnac, Quintana Paulette. "Los derechos humanos bajo la lupa de "El Decano"." Tesis, Universidad de Chile, 2007. http://repositorio.uchile.cl/handle/2250/145175.

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Memoria para optar al título de periodista<br>Esta investigación fue desarrollada en el marco del proyecto “El Diario de Agustín. El Mercurio y las violaciones a los Derechos Humanos”, de la Escuela de Periodismo de la Universidad de Chile. Y forma parte de un documental de Ignacio Agüero y del periodista Fernando Villagrán. Durante todo el año 2006 un grupo de seis memoristas trabajó en un taller a partir del cual cada uno de ellos hizo su propia investigación. El proceso fue registrado por las cámaras del documental.
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Jewson, Stephen P. "Decadal and interdecadal climate variability." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308590.

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Shen, Hong. "Mitogenomic analysis of decapod phylogeny." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2012. http://dx.doi.org/10.18452/16505.

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Für eine umfassende Untersuchung der Phylogenie der Decapoda wurden von mir die mitochondrialen Genome von 13 Dekapoden sequenziert. Zusammen mit den in der GenBank verfügbaren Sequenzen von 31 Dekapoden und dem von der Universität Bonn zur Verfügung gestellten mitochondrialen Genom von Dromia personata deckt dieser Datensatz alle großen Teilgruppen der Decapoda ab. Maximum likelihood (ML)-Analysen und Bayesian inference (BI)-Analysen der Nucleotidsequenzen und Aminosäuresequenzen ergaben bezüglich der Verwandtschaft der hochrangigen Taxa ähnliche Topologien: (((((((Anomala, Brachyura), Thalassinida: Gebiidea) Thalassinida: Axiidea), Astacidea), Achelata), Stenopodidea), Caridea), Dendrobranchiata). Gleichwohl wurde mit den Polychelida ein problematisches Taxon mit ungewissen Verwandtschaftsbeziehungen identifiziert. Auf der Eben der Unterordnungen sind die Thalassinida paraphyletisch, was mit einigen morphologischen und einigen jüngeren molekularen Studien konsistent ist, alle anderen gebräuchlichen Taxa sind monophyletisch. Es handelt sich um eine Inversion, die sich vom S-E-F tRNA cluster bis zum I-Q-M tRNA cluster erstreckt und in Procambarus fallax f. virginalis und Homarus gammarus auftritt. Im Vergleich mit dem Genarrangement des Limulus polyphemus zeigen beide Astaciden in dieser Region exakt dieselbe Inversion wie der Priapulide Priapulus caudatus, die daher innerhalb der Ecdysozoa als konvergent angenommen werden muss. Auch neben dieser Inversion innerhalb der Astacidea zeigen die Genarrangements aller verfügbaren Dekapoden mehrere interessante Eigenschaften. Um die beobachteten einzigartigen genomischen Eigenschaften zu erklären, schlage ich mit dem „inversion triggered duplication“ Model ein neues Modell für Gen-Rearrangements vor.<br>For a comprehensive study of decapod phylogeny at the mitochondrial genome level, I have sequenced the mitochondrial genome of 13 decapods. Together with available sequences of 31 decapods from GenBank, and the mitochondrial genome of Dromia personata provided by the Bonn University, the dataset now cover all major decapod taxa. Maximum likelihood (ML) and Bayesian inference (BI) of the nucleotide and amino acid datasets reveal similar topologies at the higher level relationships: (((((((Anomala, Brachyura), Thalassinida: Gebiidea) Thalassinida: Axiidea), Astacidea), Achelata), Stenopodidea), Caridea), Dendrobranchiata). Nevertheless, one problematic taxon, Polychelida, with ambiguous affinities is recognized. At the lower level, most taxa are monophyletic, whereas the Thalassinida is paraphyletic, which is consistent with some morphological and molecular results. An inversion spanning from S-E-F tRNA cluster to the I-Q-M tRNA cluster occurred in Procambarus fallax f. virginalis, Homarus gammarus, and one priapulid Priapulus caudatus. Compared with the gene arrangement of the horseshoe crab Limulus polyphemus, both astacids and the priapulid exhibit the same inversion, which is therefore supposed to be a convergent event of the clade Astacidea and Priapulida among Ecdysozoa. Other than this notable feature observed in astacids, the gene arrangements in all available decapods show some interesting characters. To explain these unique genomic features observed here, a new gene rearrangement model is proposed, which is called the “inversion triggered duplication” model.
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Books on the topic "Decanol"

1

Antonio, Ruiz José. El decano. ERM, 1995.

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Ballester, Gonzalo Torrente. La muerte del decano. Planeta, 1992.

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Erazo, Fernando Valenzuela. La Rebelión de los decanos. Ediciones Copygraph, 1993.

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Erazo, Fernando Valenzuela. La rebelión de los decanos. Ediciones Copygraph, 1993.

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Villemaux, Francis. Décapod: Gueules noires & trafic lourd : les grandes années de la traction vapeur sur l'artère nord-est. La Régordane, 1992.

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Canada, Environment Canada Fisheries and Oceans. Decapod crustacea of the Atlantic Coast of Canada. Environment Canada., 1990.

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Anderson, David L. T., and Jürgen Willebrand, eds. Decadal Climate Variability. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03291-6.

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PGDip, Jackson Gavin BA, ed. Book of decamot. Xlibris, 2015.

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Iorio, Arturo De. Coram De Iorio decano sententiae selectae. Monitor Ecclesiasticus, 1985.

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Antúnez, Marcos Silvera. Club Atlético Peñarol, campeón del siglo XX: Decano del fútbol uruguayo, decano del fú́́tbol rioplatense. Ediciones El Galeón, 2010.

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Book chapters on the topic "Decanol"

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Thiele, T., J. F. Berret, S. Müller, and C. Schmidt. "Rheology and NMR Measurements of Sodium Dodecyl Sulphate/Decanol/Water Nematics." In Progress and Trends in Rheology V. Steinkopff, 1998. http://dx.doi.org/10.1007/978-3-642-51062-5_261.

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Patton, C. L., S. H. Kisler, and K. D. Luks. "Multiphase Equilibrium Behavior of a Mixture of Carbon Dioxide, 1-Decanol, andn-Tetradecane." In ACS Symposium Series. American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0514.ch005.

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Bährle-Rapp, Marina. "Decanal." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2669.

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Acharya, D. P., E. Oshimura, K. Sakamoto, and H. Kunieda. "The lyotropic ribbon phase and its transformation to the lamellar phase in the potassium N-dodecanoyl-dl-alaninate/water/decanol system." In Trends in Colloid and Interface Science XVII. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/b93969.

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Wohlfarth, Ch. "Viscosity of decanal." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_353.

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Wallace, John M. "Observed Climatic Variability: Spatial Structure." In Decadal Climate Variability. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03291-6_2.

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Wallace, John M. "Observed Climatic Variability: Time Dependence." In Decadal Climate Variability. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03291-6_1.

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Olbers, Dirk, and Christoph Völker. "Steady States and Variability in Oceanic Zonal Flows." In Decadal Climate Variability. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03291-6_10.

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Ghil, Michael, and Pascal Yiou. "Spectral Methods: What They Can and Cannot do for Climatic Time Series." In Decadal Climate Variability. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03291-6_11.

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Palmer, T. N. "Predictability of the Atmosphere and Oceans: From Days to Decades." In Decadal Climate Variability. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-662-03291-6_3.

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Conference papers on the topic "Decanol"

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Zhu, Beibei, and Hongtao Gao. "Molecular Dynamics Simulation for the Impact of N-Decanol Surfactants on the Liquid-Vapor Interface of Lithium Bromide Aqueous Solution." In 2010 14th International Heat Transfer Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/ihtc14-22746.

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In order to investigate the effect of n-decanol, a kind of alcohol surfactants, on the absorption of water vapor into lithium bromide aqueous solution, this study focused on microscopic structure of the liquid-vapor interface of the electrolyte solution, the impact of n-decanol molecules on the interfacial properties and the absorption dynamic process employing the method of molecular dynamics simulation. The liquid-vapor configuration of lithium bromide aqueous solution added with four concentration of n-decanol can be analyzed by examining the density profile, the radial distribution functions and orientational order parameter. The computed results revealed that n-decanol molecules tended to adsorb at the interface with the methyl group pointing into the vapor phase and hydrophilic hydroxyl group pointing into the liquid phase which do much help to form a hydrogen bond network with water, and the tendency of this kind of preferred orientation became distinct with the increase of the amount of n-decanol. The hydrocarbon chains of n-decanol molecules were inclined to close to stay upright near the interface while the monolayer of n-decanol came into being near the interface. Ions were repelled from the surface. The direct interactions between hydroxyl hydrogen of n-decanol and anion exist, and there are much stronger electrostatic interactions between oxygen of n-decanol and cation. The dynamic process of the absorption of water into aqueous electrolyte solution with or without n-decanol was explored by molecular dynamics simulation under non equilibrium conditions. The simulation results showed that in comparison to the lithium bromide aqueous solution without n-decanol, the electrolyte aqueous solution with n-decanol can absorb more water molecules distinctly for 100 ps.
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Mao, Xuehua. "Solvent extraction of iron (III) from chloride acid solutions by decanol." In 3rd International Conference on Material, Mechanical and Manufacturing Engineering (IC3ME 2015). Atlantis Press, 2015. http://dx.doi.org/10.2991/ic3me-15.2015.24.

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Moriya, Shinji, Fukuo Yaginuma, Hiroichi Watanabe, Daisuke Kodama, Masahiro Kato, and Naotsugu Isshiki. "Utilization of Ethanol and Gas Oil Blended Fuels for Diesel Engine (Addition of Decanol and Isoamyl Ether)." In 34th Intersociety Energy Conversion Engineering Conference. SAE International, 1999. http://dx.doi.org/10.4271/1999-01-2518.

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Moore, Berrien. "The Decadal Survey." In Conference on Lasers and Electro-Optics. OSA, 2009. http://dx.doi.org/10.1364/cleo.2009.pwb1.

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Moore, Berrien. "The Decadal Survey." In International Quantum Electronics Conference. OSA, 2009. http://dx.doi.org/10.1364/iqec.2009.pwb1.

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Squyres, Steven W. "The NRC planetary decadal survey." In 2011 IEEE Aerospace Conference. IEEE, 2011. http://dx.doi.org/10.1109/aero.2011.5747218.

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RUGGIERO, PETER, JEREMY MULL, PHOEBE ZARNETSKE, SALLY HACKER, and ERIC SEABLOOM. "INTERANNUAL TO DECADAL FOREDUNE EVOLUTION." In The Proceedings of the Coastal Sediments 2011. World Scientific Publishing Company, 2011. http://dx.doi.org/10.1142/9789814355537_0053.

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Lee, Woohun, Geehyuk Lee, Jiseok Song, Boram Lee, and Hyunjung Kim. "Digital decal." In ACM SIGGRAPH 2009 Emerging Technologies. ACM Press, 2009. http://dx.doi.org/10.1145/1597956.1597964.

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Chapanov, Yavor, Jan Vondrák, Cyril Ron, Vasile Mioc, Cristiana Dumitrache, and Nedelia A. Popescu. "Decadal Oscillations of The Earth Rotation." In EXPLORING THE SOLAR SYSTEM AND THE UNIVERSE. AIP, 2008. http://dx.doi.org/10.1063/1.2993638.

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Balmaseda, Magdalena A., Magdalena A. Balmaseda, Magdalena A. Balmaseda, et al. "Initialization for Seasonal and Decadal Forecasts." In OceanObs'09: Sustained Ocean Observations and Information for Society. European Space Agency, 2010. http://dx.doi.org/10.5270/oceanobs09.cwp.02.

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Reports on the topic "Decanol"

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Dell, G. F., H. Hahn, G. Parzen, and A. G. Ruggiero. RHIC Decapole Correction Magnet Requirements. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/1119282.

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Rhoades-Brown, M. J., and H. Hahn. Analytic Studies of Decapole Correction Schemes. Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/1119320.

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Mather, James. ARM User Facility 2020 Decadal Vision. Office of Scientific and Technical Information (OSTI), 2021. http://dx.doi.org/10.2172/1782812.

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Abazajian, Kevork. CMB-S4 Decadal Survey APC White Paper. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1556957.

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GREENE, LAURA, TOM LUBENSKY, MATTHEW TIRRELL, et al. Frontiers of Materials Research: A Decadal Survey. Office of Scientific and Technical Information (OSTI), 2019. http://dx.doi.org/10.2172/1556101.

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Knowlton, Nancy, Emily Corcoran, Thomas Felis, et al. Rebuilding Coral Reefs: A Decadal Grand Challenge. International Coral Reef Society and Future Earth Coasts, 2021. http://dx.doi.org/10.53642/nrky9386.

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This document is the work of a team assembled by the International Coral Reef Society (ICRS). The mission of ICRS is to promote the acquisition and dissemination of scientific knowledge to secure the future of coral reefs, including via relevant policy frameworks and decision-making processes. This document seeks to highlight the urgency of taking action to conserve and restore reefs through protection and management measures, to provide a summary of the most relevant and recent natural and social science that provides guidance on these tasks, and to highlight implications of these findings for the numerous discussions and negotiations taking place at the global level.
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ZAJC, W. ET AL. PHENIX EXPERIMENT AT RHIC: DECADAL PLAN 2004-2013. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/15007043.

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Bergmann, D., C. Chuang, B. Govindasamy, P. Cameron-Smith, and D. Rotman. High Resolution Aerosol Modeling: Decadal Changes in Radiative Forcing. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/15014616.

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Staehr, T. W. Test specification for decant pump and winch assembly. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10115667.

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Ganguly, Auroop R., Poulomi Ganguli, and Devashish Kumar. Water Stress on U.S. Power Production at Decadal Time Horizons. Office of Scientific and Technical Information (OSTI), 2014. http://dx.doi.org/10.2172/1339441.

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