Academic literature on the topic 'Taiwanensis'
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Journal articles on the topic "Taiwanensis"
Lee, Chu, Lin, Kung, Lin, and Lee. "Root Traits and Biomechanical Properties of Three Tropical Pioneer Tree Species for Forest Restoration in Landslide Areas." Forests 11, no. 2 (February 5, 2020): 179. http://dx.doi.org/10.3390/f11020179.
Full textChen, Wen-Jen, Tzu-Yen Kuo, Chun-Yi Chen, Feng-Chia Hsieh, Yu-Liang Yang, Je-Ruei Liu, and Ming-Che Shih. "Whole Genome Sequencing and Tn5-Insertion Mutagenesis of Pseudomonas taiwanensis CMS to Probe Its Antagonistic Activity Against Rice Bacterial Blight Disease." International Journal of Molecular Sciences 21, no. 22 (November 16, 2020): 8639. http://dx.doi.org/10.3390/ijms21228639.
Full textFarina, Priscilla, Giuseppe Mazza, Claudia Benvenuti, Ilaria Cutino, Paolo Giannotti, Barbara Conti, Stefano Bedini, and Elisabetta Gargani. "Biological Notes and Distribution in Southern Europe of Aclees taiwanensis Kȏno, 1933 (Coleoptera: Curculionidae): A New Pest of the Fig Tree." Insects 12, no. 1 (December 23, 2020): 5. http://dx.doi.org/10.3390/insects12010005.
Full textIWATSUKI, YUKIO, and KENT E. CARPENTER. "Acanthopagrus taiwanensis, a new sparid fish (Perciformes), with comparisons to Acanthopagrus berda (Forsskål, 1775) and other nominal species of Acanthopagrus." Zootaxa 1202, no. 1 (May 15, 2006): 1. http://dx.doi.org/10.11646/zootaxa.1202.1.1.
Full textChan, Yu-Yi. "Neoclerodane Diterpenoids from Ajuga taiwanensis." CHEMICAL & PHARMACEUTICAL BULLETIN 53, no. 2 (2005): 164–67. http://dx.doi.org/10.1248/cpb.53.164.
Full textTSENG, CHING-TZU, ROGER F. HOU, and LI-CHENG TANG. "Steinernema taiwanensis n. sp. (Rhabditida: Steinernematidae), a new entomopathogenic nematode from Taiwan." Zootaxa 4434, no. 3 (June 18, 2018): 466. http://dx.doi.org/10.11646/zootaxa.4434.3.4.
Full textKourilova, Xenie, Iva Pernicova, Michaela Vidlakova, Roman Krejcirik, Katerina Mrazova, Kamila Hrubanova, Vladislav Krzyzanek, Jana Nebesarova, and Stanislav Obruca. "Biotechnological Conversion of Grape Pomace to Poly(3-hydroxybutyrate) by Moderately Thermophilic Bacterium Tepidimonas taiwanensis." Bioengineering 8, no. 10 (October 14, 2021): 141. http://dx.doi.org/10.3390/bioengineering8100141.
Full textVerma, Subhash Chandra, Soumitra Paul Chowdhury, and Anil Kumar Tripathi. "Phylogeny based on 16S rDNA andnifHsequences ofRalstonia taiwanensisstrains isolated from nitrogen-fixing nodules ofMimosa pudica, in India." Canadian Journal of Microbiology 50, no. 5 (May 1, 2004): 313–22. http://dx.doi.org/10.1139/w04-020.
Full textDoin de Moura, Ginaini Grazielli, Philippe Remigi, Catherine Masson-Boivin, and Delphine Capela. "Experimental Evolution of Legume Symbionts: What Have We Learnt?" Genes 11, no. 3 (March 23, 2020): 339. http://dx.doi.org/10.3390/genes11030339.
Full textKim, Sam Woong, Yeon Jo Ha, Kyu Ho Bang, Seungki Lee, Joo-Hong Yeo, Hee-Sun Yang, Tae-Won Kim, Kyu Pil Lee, and Woo Young Bang. "Potential of Bacteriocins from Lactobacillus taiwanensis for Producing Bacterial Ghosts as a Next Generation Vaccine." Toxins 12, no. 7 (July 1, 2020): 432. http://dx.doi.org/10.3390/toxins12070432.
Full textDissertations / Theses on the topic "Taiwanensis"
Schmutzler, Karolin [Verfasser]. "Understanding the regulatory network of biofilm formation in Pseudomonas taiwanensis VLB120 / Karolin Schmutzler." Aachen : Shaker, 2016. http://d-nb.info/1118257944/34.
Full textVolmer, Jan [Verfasser]. "Strain and process engineering to exploit solvent tolerance mechanisms of Pseudomonas taiwanensis VLB120 for asymmetric styrene epoxidation / Jan Volmer." Aachen : Shaker, 2016. http://d-nb.info/1098039130/34.
Full textLenzen, Christoph [Verfasser], Lars Mathias [Akademischer Betreuer] Blank, and Nick [Akademischer Betreuer] Wierckx. "Metabolic engineering of Pseudomonas taiwanensis VLB120 for sustainable production of 4-Hydroxybenzoate / Christoph Lenzen ; Lars M. Blank, Nick Wierckx." Aachen : Universitätsbibliothek der RWTH Aachen, 2020. http://d-nb.info/1221697528/34.
Full textDaubech, Benoît. "Évolution expérimentale d'un symbiote de légumineuse : étude des facteurs génétiques et des forces de sélection qui favorisent ou non l'évolution du mutualisme." Thesis, Toulouse 3, 2019. http://www.theses.fr/2019TOU30338.
Full textThe symbiosis between legumes and bacteria, known as rhizobia, is a complex process resulting in the formation of a novel plant organ, the nodule, in which internalized bacteria (bacteroids) fix nitrogen to the benefit of the host plant. Rhizobia do not form a homogeneous taxonomic group. They belong to a dozen of genera scattered within α- and ß-proteobacteria. Rhizobia may have evolved from horizontal transfer of key symbiotic genes, followed by genome remodeling under plant selection pressure, allowing the activation and/or optimization of the acquired symbiotic potential. This evolutionary scenario is being replayed in the laboratory using an experimental evolution approach. The symbiotic plasmid of the Mimosa pudica symbiont, Cupriavidus taiwanensis LMG19424, was introduced into the plant pathogen Ralstonia solanacearum GMI1000. 18 parallel lineages were derived from this chimeric ancestor using serial cycles of inoculation with M. pudica and re-isolation of bacteria from the nodules. After 16 cycles of evolution, three observations were done: i) the evolved bacteria do not fix nitrogen and evolution towards mutualism is not completed, ii) a gene of unknown function seems to be involved in intracellular infection and iii) the mutations that allow and/or improve intracellular infection also improve nodulation capacity. To determine conditions that favor the emergence of mutualism in the laboratory and possibly in nature, we analyzed the spatio-temporal dynamics of two quasi-isogenic sub-populations of C. taiwanensis, one nitrogen-fixing (Fix+) and the other not (Fix-), along their symbiotic process with M. pudica. We observed an early degenerescence of Fix- bacteroids, even when they share a nodule with Fix+, and established the kinetics of Fix+ expansion along time. Using mathematical modeling and experimental validations, we predicted that rare Fix+ will invade a population dominated by non-fixing bacteria during serial nodulation cycles with a probability that is function of initial inoculum, plant population size and nodulation cycle length. Then, we studied the role of a C. taiwanensis symbiotic plasmid gene, whose deletion in one lineage was responsible of intracellular infection defect. We showed that this gene, called noeM, is a novel nodulation gene involved in the biosynthesis of atypical Nod factors where the reducing sugar is open and oxidized. noeM was mostly found in isolates of the Mimoseae tribe, especially in all strains able to nodulate M. pudica. The noeM genes form a separate phylogenetic clade containing only rhizobial genes. A noeM deletion mutant of C. taiwanensis was affected for the nodulation of M. pudica confirming the role of noeM in the symbiosis with this legume. Last, we initiated the detailed cytological analysis of M. pudica root infection by C. taiwanensis and a few strains bearing adaptive mutations for intracellular infection, in order to analyze the effect of these mutations on early symbiotic stages
Wynands, Benedikt [Verfasser], Lars Mathias [Akademischer Betreuer] Blank, and Nick [Akademischer Betreuer] Wierckx. "Engineering of Pseudomonas taiwanensis VLB120 for the sustainable production of hydroxylated aromatics / Benedikt Niklas Daniel Wynands ; Lars Mathias Blank, Nick Wierckx." Aachen : Universitätsbibliothek der RWTH Aachen, 2019. http://d-nb.info/1193734770/34.
Full textAbalain-Colloc, Marie-Louise. "Spiroplasmes de moustiques : caractérisation de deux nouvelles espèces Spiroplasma sabaudiense et Spiroplasma taiwanense : classification du groupe XVI des spiroplasmes." Brest, 1991. http://www.theses.fr/1991BRES2003.
Full textChang, Yung-Ta, and 張永達. "Physiological Studies on Isoetes Taiwanensis DeVol." Thesis, 1987. http://ndltd.ncl.edu.tw/handle/11129208826296264661.
Full text國立臺灣師範大學
生物學系
75
In the leaves (but not corms) of the submerged aquatic plant Isoetes taiwanensis, both in the field and greenhouse, malic acid concentration fluctuates from 10-13mg/gfw in the morning to 1-3 mg/gfw in the evening. Associated with this is a change in pH (a. m. pH 3-4 vs. p. m. pH 5-6) and titrable acidity (220-20 ueq/gfw change in acidity between morning and evenign) of the plant extract, It is obvious that Isoetes taiwanensis is a CAM plant. The change of malic acid and titrable acidity are decreased when the leaves emerged. It is suggested that CAM in Isoetes taiwanensis may be related to the lower availability of CO2 for photosynthesis during the day than during the night, and short time high intensity light. The stomata are closed when the leaf submerged; and open when the leaf emerged. After 2 hours the leaf expose to air, the open ratio is 100%; but when the leaf submerged again, the closed ratio is only about 85% after 10 hours. We find the movement of guard cells are controlled by the subsidary cells from the S. E. M. and paraffin method''s observations.
周家怡. "Development of Ascogregarina taiwanensis in Aedes albopictus." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/51163646088701814203.
Full text高雄醫學大學
醫學研究所
82
Ascogregarina taiwanensis, originally reported from the mosquito Aedes albopictus collected in Taiwan, belongs to the Phylum Apicomplexa, the Class Sporozoa, the Order Gregarina, the suborder Aseptatina and the Family Lecudinidae in taxonomy. In this study, ultrastructures in various stages of the parasite and its life cycle in the mosquito host were investigated by using light and electron microscopy. The result showed that sporozoites were soon releasedfrom ingested oocysts in the lumen of the midgut and then penetrated into the epithelium, forming the intracellular stage. Subsequently, the parasite left the epithelium and develope into the extracellular stage trophozoite in 2 days. The fine structures of A. taiwanensis, intracellular or extracellular, showed that the surface of the parasite consisted of two distinct layers. The outer layer was always thicker than the inner one. There usually were groups of small dots, called as subpellicular fibrils, right under the inner membrane. Fibrils in each group appeared to be parallel. The cytoplasma of the parasite can be divided into two parts. The outer part-ectoplasma contained relatively fine granules while the contents of the inner part- endoplasma was full of rough granules. In fact, many organelles including endoplasmic reticulum, mitochondria, ribosomes and dense granules can be seen in both parts of the cytoplasma. However, some other organelles such as vacuoles, droplets and paraglycogens appeared only in the ectoplasma. Usually, there is a mitochondria zone in the space between the protomerite and the deutomerite. As a usual, the late stage of the trophozoites migrated into the Malpighian tubules when the mosquito pupated. One of interesting findings in this study is that the trophozoite twisted off to remove most body except the portion containing the nucleus. The resulting spherical or elliptic gametes subsequently paired up to become the early stage of the gametocyst. A number of oocysts were then matured in each gametocyst before they were expelled with excreta into the breeding site. The ultrastructural studies showed that a septum was formed in the middle of the newly-formed, i.e., primary gametocyst. Subpellicular fibrils can be seen on both sides of the multi-layered septum, indicating the septum was derived from fusing of two parasite surfaces. It seems that the capsule surrounding the early gametocyst tended to fuse with surface membrane of the parasites which were conjugating, resulting in a thicker outer membrane. The septum subsequently disappeared, leading to form a more mature gametocyst containing fine granules. The contents of the developing gametocyst later became relatively rough, in which a mass of cytoplasma containing a number of vacuoles were formed. Later on, the cytoplasmic mass cleavaged into many small pieces. Each piece was finally transformed into an individual oocyst. As a matter of fact, the oocyst with defined shape was formed 2 days post pupation. According to the observations in this study, the gametocyst of the 3rd day pupae was full of numerous oocysts which were released when the gametocyst were pressed. In consequence, the oocyst further matured to be a lemon shape with plugs on both ends. During the late developing stage, vacuoles and granules within the oocyst disappeared gradually. The complete mature oocyst containing 8 sporozoites was usually formed 2 days after emergence. Ultrastructurally, the distinct organelles of the sporozoite included a monolayered-surface membrane, 2 preconid polar rings and one polar ring in its anterior portion. In addition, subpellicular microtubules, including an internal tubules, origined from the polar ring was pretty close to rhopties. In conclusion of the life cycle study, a sexual reproductive process distinguished from those occurring in other apicomplexan arised. Eventually, the "pseudoconjugatio", which has been thought to occur before gametes were formed, was a true conjugation in this gregarine parasite. Perhaps this reproduction behavior isadaptable to most of the related species.
郭瓊華. "The Population Genetic Structrue of Sphenomorphus taiwanensis." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/00548180853602994416.
Full text國立臺灣師範大學
生物研究所
90
Sphenomorphus taiwanensis is an endemic species of Taiwan. It was distributed above 2000 m attitude. Currently, most phylogeographic studies focused on lower attitude species. To high attitude species,living in high mountains was like living in an isolation island. The geological isolation may influence the population genetic structure of S. taiwanensis. Cytochrome b (Cyt b) and cytochrome oxidase c subunit 1 (COX1) were used as genetic markers to analysis the phylogeography of S. taiwanensis. The partial sequences were determined in 89 individuals. 56 and 48 haplotype were identified. The maximum pairwise genetic distance between individuals within population was 10.6% (Cyt b) and 10.4% (COX1). The maximum pairwise genetic distances between individuals between populations were 16.6% (Cyt b) and 11.2% (COX1). The mean pairwise genetic distance within population were 0.4~9.8% (Cyt b) and 0~5.7% (COX1). The mean pairwise genetic distance between populaitons were 3.2~13.9% (Cyt b) and 1.6~10.4% (COX1). We found that the intraspecies genetic variation of S. taiwanensis was larger than other species. The gene flow index indicated that the gene flows among populations were hindered. It indicated that the differentiation level among populations was high, but was not consistent with isolation by distance model. We found the gene flows between Hsuehshan population and other populations were hindered. We thought Hsuehshan population was an special isolation population. Phylogenetic trees were constructed by neighbor-joining (NJ) and maximum parsimony (MP) methods using S. incognitus and S. indicus as the outgroups indicated that S. taiwanensis can be separated into nine major lineages with high bootstrap value. Some lineages were allopatric, others were sympatric. The lineages’ distribution was not consistent with the geological distribution of populations. Some populations only had one lineage, included Hsuehshan, Tahsuehshan, Hohuanshan, Alishan, Yakou population. Kuanwu and Taipingshan population had two lineages, Tatachia population had three lineages, and Nanhu population had four lineages. The genetic diversity of Nanhu population was very high. The reason of that there were high intraspecies genetic variation of S. taiwanensis may be multiple invasion or refuge effect or radiation evolution.
Chen, Cuan-wei, and 陳冠瑋. "Embryology in Maackia taiwanensis Hoshi et Ohashi." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/68753218534479994184.
Full text國立臺灣大學
森林學研究所
93
Maackia taiwanensis Hoshei et Ohashi is an endemic species to Taiwan which belong to the Fabaceae, Faboideae. Trees are deciduous. Bisexual flowers are produced from early August to late August. The pods are maturing in December. Inflorescence primordia are formed at shoot apices in mid April. The primordia of calyx occur in late April. The primordial of petal, stamen and pistl occur successively from early June to late June. Calyx 5-lobed;petal 5, consisting of one standard, two wing and two keel-petal. Stamens 10, two whorls and anther are tetrasporangiate. The pistil is mono-carpellary with gynophore. Young anthers are composed of a protoderm and a central cell mass in early July. The anther wall layers consist of an epidermis, one layered endothecium, two middle layers and a tapetum of one layer. The development of anther wall layer belongs to the basic type. The tapetum is of the glandular type. Pollen mother cells undergo meioses through simultaneous cytokinesis and give rise to tetrads of microspores, which are tetrahedrally arranged. Mature pollen grains are 2-celled, globose, 3-colporate and 15~20μm in diameter. Anther dehiscence is longitudinal. The pistil with 2 to 5 ovules on a marginal placentation. Ovules are campylotropous, bitegamic. The outer integument is composed of 3 to 6 layers of cells in thickness, while the inner integument is of 2 layers of cells. The inner integument is degenerated during the seeds development. The megaspore mother cell is located 4-6 layers of cells beneath the epidermis at the nucellus top end. So it defined as crassinucellate. The megaspore mother cell divides transversally to form a linear megaspore tetrad. The megaspore at the chalazal end develops into the embryo sac mother cell. The development of embryo sac is Polygonum type. The two polar nuclei fuse before fertilization and the the three antipodal cells degenerate soon after fertilization. Multi-embryo sac might occasionally occur in an ovule. The endosperm deveolops through nuclei multiplication and is degenerated at seed maturing. Seeds consist of an embryo without endosperm.
Book chapters on the topic "Taiwanensis"
Lim, T. K. "Hibiscus taiwanensis." In Edible Medicinal and Non Medicinal Plants, 381–84. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-8748-2_26.
Full textMehlhorn, Heinz. "Ascogregarina taiwanensis." In Encyclopedia of Parasitology, 234. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_288.
Full textMehlhorn, Heinz. "Ascogregarina taiwanensis." In Encyclopedia of Parasitology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-27769-6_288-2.
Full textWang, John Y., Kimberly N. Riehl, Michelle N. Klein, Shiva Javdan, Jordan M. Hoffman, Sarah Z. Dungan, Lauren E. Dares, and Claryana Araújo-Wang. "Biology and Conservation of the Taiwanese Humpback Dolphin, Sousa chinensis taiwanensis." In Advances in Marine Biology, 91–117. Elsevier, 2016. http://dx.doi.org/10.1016/bs.amb.2015.07.005.
Full textConference papers on the topic "Taiwanensis"
Siripornadulsil, Surasak, and Wilailak Siripornadulsil. "Characterization of Cadmium-Resistant Bacteria and Their Application for Cadmium Bioremediation." In ASME 2009 12th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2009. http://dx.doi.org/10.1115/icem2009-16072.
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