Academic literature on the topic 'Jatropha curcas'
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Journal articles on the topic "Jatropha curcas"
Menezes, Ritesh G., Nageshkumar G. Rao, Suman S. Karanth, Asha Kamath, Shahnavaz Manipady, and V. V. Pillay. "Jatropha curcas poisoning." Indian Journal of Pediatrics 73, no. 7 (July 2006): 634. http://dx.doi.org/10.1007/bf02759934.
Full textKulkarni, M. L., H. Sreekar, K. S. Keshavamurthy, and Nivedita Shenoy. "Jatropha curcas-poisoning." Indian Journal of Pediatrics 72, no. 1 (January 2005): 75–76. http://dx.doi.org/10.1007/bf02760586.
Full textAbobatta, Waleed. "Jatropha curcas: an overview." JOURNAL OF ADVANCES IN AGRICULTURE 10 (February 28, 2019): 1650–56. http://dx.doi.org/10.24297/jaa.v10i0.8145.
Full textNurhidayanti, Nurhidayanti. "Acute Toxicity Test of Jatropha curcas L. on Nile Tilapia Seeds (Oreochromis niloticus L.)." Science and Technology Indonesia 5, no. 1 (January 30, 2020): 18. http://dx.doi.org/10.26554/sti.2020.5.1.18-22.
Full textRužbarský, Juraj, Miroslav Müller, Jan Mareček, and Milan Geršl. "Jatropha curcas – Analysis of Gross Calorific Value." Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis 62, no. 6 (2014): 1381–84. http://dx.doi.org/10.11118/actaun201462061381.
Full textPatade, Vikas Yadav, Deepti Khatri, Kamal Kumar, Atul Grover, Maya Kumari, Sanjay Mohan Gupta, Devender Kumar, and Mohammed Nasim. "RNAi Mediated curcin precursor gene silencing in Jatropha (Jatropha curcas L.)." Molecular Biology Reports 41, no. 7 (February 27, 2014): 4305–12. http://dx.doi.org/10.1007/s11033-014-3301-8.
Full textWen, Yuan Guang, Hong Guang Zhu, Min Tang, Fang Chen, Lin Tang, and Ying Xu. "The Distribution And Resource Evaluation of Typical Energy Plants (Jatropha curcas L.) in Guangxi, China." Advanced Materials Research 433-440 (January 2012): 1333–37. http://dx.doi.org/10.4028/www.scientific.net/amr.433-440.1333.
Full textSettineri, Giovanna, Maria Rosaria Panuccio, and Adele Muscolo. "Jatropha Curcas Sludge Valorization." Procedia - Social and Behavioral Sciences 223 (June 2016): 865–70. http://dx.doi.org/10.1016/j.sbspro.2016.05.295.
Full textAnguessin, Benjamine, Pierre Marie Mapongmetsem, Adamou Ibrahima, and Guidawa Fawa. "Effet de la fertilisation organique à base de litière foliaire de Jatropha curcas L. et Jatropha gossypifolia L. sur la culture de tomate (Lycopersicon esculentum Mill.) à Guider (Nord/Cameroun)." International Journal of Biological and Chemical Sciences 15, no. 2 (June 22, 2021): 524–35. http://dx.doi.org/10.4314/ijbcs.v15i2.12.
Full textNiagita Wiratni, Ni Made, I. Nyoman Jirna, and IGA Sri Dhyanaputri. "Potensi Antifungi Tangkai Daun Jarak Pagar Terhadap Pertumbuhan Candida albicans." Medical Laboratory Technology Journal 3, no. 2 (December 29, 2017): 63. http://dx.doi.org/10.31964/mltj.v3i2.169.
Full textDissertations / Theses on the topic "Jatropha curcas"
Lima, Magda Laiara Bezerra de. "OrganogÃnese in vitro em Jatropha curcas L." Universidade Federal do CearÃ, 2013. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=9729.
Full textO pinhÃo manso (Jatropha curcas L.) à considerado uma fonte potencial para a produÃÃo de biocombustÃveis, tendo por base a alta produtividade e qualidade do Ãleo extraÃdo de suas sementes. Entretanto, seu uso à inviabilizado para alimentaÃÃo humana e animal devido à presenÃa de fatores antinuticionais como a curcina e, em especial, os Ãsteres de forbol. A utilizaÃÃo de ferramentas biotecnolÃgicas, como a cultura de tecidos, pode vir a minimizar ou solucionar essas limitaÃÃes. Nesse contexto, o objetivo desse trabalho foi propagar in vitro plantas inteiras via cultivo de Ãpices caulinares obtidos a partir de sementes de pinhÃo manso germinadas in vivo e in vitro; determinar a reprodutibilidade de um protocolo de regeneraÃÃo disponÃvel na literatura e definir, atravÃs de estudos histolÃgicos, a origem da planta regenerada in vitro. Para a propagaÃÃo in vitro utilizou-se Ãpices caulinares, como explantes, que foram colocados em meio MS suplementado com as citocininas BAP (6-benzilaminoprina), KIN (cinetina) e 2-iP (2-isopenteniladenina) na concentraÃÃo de 2,0 mg.L-1. O BAP apresentou os melhores resultados no desenvolvimento dos Ãpices caulinares. Este e a giberelina foram utilizados juntos no mesmo meio ou separados, para a induÃÃo do alongamento dos mesmos. O Ãcido indol-3-butirÃco (AIB) foi usado para o enraizamento. A suplementaÃÃo do meio de cultura com BAP foi eficiente no desenvolvimento dos Ãpices caulinares e o alongamento apresentou Ãxito com o uso do GA3 individualmente. O enraizamento com o AIB foi conseguido. A fim de determinar a reprodutibilidade do protocolo de organogÃnese, cotilÃdones de sementes de pinhÃo manso germinadas in vitro foram colocados em meio MS suplementado com BAP e AIB para a induÃÃo da formaÃÃo de partes aÃreas, estas foram alongadas com BAP e enraizadas com AIB. AlÃm disso, os explantes cotiledonares foram colocados com a face abaxial e adaxial em contato com o meio de cultivo a fim de estabelecer a melhor posiÃÃo do mesmo na regeneraÃÃo in vitro. Plantas inteiras de J. curcas L. foram obtidas a partir da utilizaÃÃo do protocolo testado. A melhor posiÃÃo do segmento cotiledonar foi a face adaxial em contato com o meio, onde 56% dos explantes formaram partes aÃreas. A anÃlise histolÃgica foi feita com a coleta de explantes cotiledonares em intervalos sequenciais de 0, 5, 10, 15 e 25 dias de permanÃncia do meio de regeneraÃÃo. O estudo anatÃmico possibilitou o acompanhamento da organogÃnese do pinhÃo manso, no qual cÃlulas parenquimÃticas prÃximas à regiÃo adaxial do explante cotiledonar se dividiram e formaram as partes aÃreas. Os dados obtidos nesse trabalho mostraram que ambos os protocolos utilizados, a partir de Ãpices caulinares e de explantes cotiledonares, foram eficientes no processo de regeneraÃÃo; as anÃlises histolÃgicas sugerem que a regeneraÃÃo ocorre via organogÃnese direta e possivelmente apresenta origem multicelular.
The physic nut (Jatropha curcas L.) is considered a potential source for the biofuel production, because of its high productivity and oil quality extracted from the seeds. However, its use is unfeasible for human and animal food due to antinutritional factors like the curcin protein and specially the secondary metabolites â phorbol esters. The application of biotechnological tools, like tissue culture, can be used to overcome these limitations. In this context, the aim of this work was to propagate whole plants in vitro using shoot cultures obtained from physic nut seeds germinated in vitro and in vivo; to determine the reproducibility of a regeneration protocol available in the literature, and to define through histological studies, the origin of the regenerated plant in vitro. For the in vitro propagation, shoots were used as explants sources, which were placed on MS medium supplemented with the cytokinins BAP (6- benzylaminopurine), KIN (kinetin) e 2-iP (2- isopentenyl adenine), 2,0 mg.L-1. BAP showed the best results in the development of the shoots. This regulator was used alone or in association with gyberelins for the elongation of the shoots. The indole-3-butyric-acid was used for the rooting. The supplementation of the medium culture with BAP was efficient in the development of the shoots and the elongation was superior with the use of GA3 alone. The rooting was achieved with AIB. To determine the reproducibility of an organogenesis protocol, cotyledons from physic nut seeds germinated in vitro were placed on MS medium supplemented with BAP and AIB for the promotion of aerial which were elongated with BAP and rooting with AIB. The cotyledonary explants were placed with the abaxial and adaxial face in contact with the medium to establish the best position of it in the in vitro regeneration. Whole plants of J. curcas L. were obtained using the protocol tested. The best position of the cotyledonar segment was the adaxial face in contact with the medium, where 56% of the explants formed shoots. The histological analysis was made with cotyledonary explants collected in sequential intervals of 0, 5, 10, 15 e 25 days of permanency in the regeneration medium. The anatomical study allowed the accompaniment of the organogenesis in physic nut, where parenchymal cells next to the adaxial region of the cotyledonar explants were divided and formed the shoots. The data obtained from this work showed that both protocols used, from shoots tips and cotyledonar explants, were efficient in the regeneration process; the histological analysis suggests that regeneration occurs via direct organogenesis and possibly presents multicellular origin.
Lima, Magda Laiara Bezerra de. "Organogênese in vitro em Jatropha curcas L." reponame:Repositório Institucional da UFC, 2013. http://www.repositorio.ufc.br/handle/riufc/8630.
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The physic nut (Jatropha curcas L.) is considered a potential source for the biofuel production, because of its high productivity and oil quality extracted from the seeds. However, its use is unfeasible for human and animal food due to antinutritional factors like the curcin protein and specially the secondary metabolites – phorbol esters. The application of biotechnological tools, like tissue culture, can be used to overcome these limitations. In this context, the aim of this work was to propagate whole plants in vitro using shoot cultures obtained from physic nut seeds germinated in vitro and in vivo; to determine the reproducibility of a regeneration protocol available in the literature, and to define through histological studies, the origin of the regenerated plant in vitro. For the in vitro propagation, shoots were used as explants sources, which were placed on MS medium supplemented with the cytokinins BAP (6- benzylaminopurine), KIN (kinetin) e 2-iP (2- isopentenyl adenine), 2,0 mg.L-1. BAP showed the best results in the development of the shoots. This regulator was used alone or in association with gyberelins for the elongation of the shoots. The indole-3-butyric-acid was used for the rooting. The supplementation of the medium culture with BAP was efficient in the development of the shoots and the elongation was superior with the use of GA3 alone. The rooting was achieved with AIB. To determine the reproducibility of an organogenesis protocol, cotyledons from physic nut seeds germinated in vitro were placed on MS medium supplemented with BAP and AIB for the promotion of aerial which were elongated with BAP and rooting with AIB. The cotyledonary explants were placed with the abaxial and adaxial face in contact with the medium to establish the best position of it in the in vitro regeneration. Whole plants of J. curcas L. were obtained using the protocol tested. The best position of the cotyledonar segment was the adaxial face in contact with the medium, where 56% of the explants formed shoots. The histological analysis was made with cotyledonary explants collected in sequential intervals of 0, 5, 10, 15 e 25 days of permanency in the regeneration medium. The anatomical study allowed the accompaniment of the organogenesis in physic nut, where parenchymal cells next to the adaxial region of the cotyledonar explants were divided and formed the shoots. The data obtained from this work showed that both protocols used, from shoots tips and cotyledonar explants, were efficient in the regeneration process; the histological analysis suggests that regeneration occurs via direct organogenesis and possibly presents multicellular origin.
O pinhão manso (Jatropha curcas L.) é considerado uma fonte potencial para a produção de biocombustíveis, tendo por base a alta produtividade e qualidade do óleo extraído de suas sementes. Entretanto, seu uso é inviabilizado para alimentação humana e animal devido à presença de fatores antinuticionais como a curcina e, em especial, os ésteres de forbol. A utilização de ferramentas biotecnológicas, como a cultura de tecidos, pode vir a minimizar ou solucionar essas limitações. Nesse contexto, o objetivo desse trabalho foi propagar in vitro plantas inteiras via cultivo de ápices caulinares obtidos a partir de sementes de pinhão manso germinadas in vivo e in vitro; determinar a reprodutibilidade de um protocolo de regeneração disponível na literatura e definir, através de estudos histológicos, a origem da planta regenerada in vitro. Para a propagação in vitro utilizou-se ápices caulinares, como explantes, que foram colocados em meio MS suplementado com as citocininas BAP (6-benzilaminoprina), KIN (cinetina) e 2-iP (2-isopenteniladenina) na concentração de 2,0 mg.L-1. O BAP apresentou os melhores resultados no desenvolvimento dos ápices caulinares. Este e a giberelina foram utilizados juntos no mesmo meio ou separados, para a indução do alongamento dos mesmos. O ácido indol-3-butiríco (AIB) foi usado para o enraizamento. A suplementação do meio de cultura com BAP foi eficiente no desenvolvimento dos ápices caulinares e o alongamento apresentou êxito com o uso do GA3 individualmente. O enraizamento com o AIB foi conseguido. A fim de determinar a reprodutibilidade do protocolo de organogênese, cotilédones de sementes de pinhão manso germinadas in vitro foram colocados em meio MS suplementado com BAP e AIB para a indução da formação de partes aéreas, estas foram alongadas com BAP e enraizadas com AIB. Além disso, os explantes cotiledonares foram colocados com a face abaxial e adaxial em contato com o meio de cultivo a fim de estabelecer a melhor posição do mesmo na regeneração in vitro. Plantas inteiras de J. curcas L. foram obtidas a partir da utilização do protocolo testado. A melhor posição do segmento cotiledonar foi a face adaxial em contato com o meio, onde 56% dos explantes formaram partes aéreas. A análise histológica foi feita com a coleta de explantes cotiledonares em intervalos sequenciais de 0, 5, 10, 15 e 25 dias de permanência do meio de regeneração. O estudo anatômico possibilitou o acompanhamento da organogênese do pinhão manso, no qual células parenquimáticas próximas à região adaxial do explante cotiledonar se dividiram e formaram as partes aéreas. Os dados obtidos nesse trabalho mostraram que ambos os protocolos utilizados, a partir de ápices caulinares e de explantes cotiledonares, foram eficientes no processo de regeneração; as análises histológicas sugerem que a regeneração ocorre via organogênese direta e possivelmente apresenta origem multicelular.
Machahua, González Miguel. "Variabilidad morfológica en poblaciones de Jatropha curcas L. "piñón blanco" (Euphorbiaceae)." Bachelor's thesis, Universidad Nacional Mayor de San Marcos, 2010. https://hdl.handle.net/20.500.12672/917.
Full text--- We analyzed the morphological variation of Jatropha curcas in 20 populations grown in the regions of Lambayeque, Piura, Tumbes, San Martin and Ucayali. A total of 123 individuals with DBH 2-4 cm were sampled, eight morphometric parameters were evaluated such as total plant height, number of branches of the plant, number of lobes of the lamina, length of blade, petiole, fruit and seed. The parameters were analyzed by Paired t test ANOVA (p less than 0.05), those with significant differences were performed principal components analysis. There are significant differences among the populations in seven parameters; regarding the total plant height, the highest value recorded was in La Libertad, and the lowest value for the population of San Isidro; regarding the number of branches, the highest value recorded was in Olmos, and the lowest value for Chazuta; regarding the length of the blade and petiole, the highest value recorded was found in Tambo Grande, and the lowest value in Olmos, regarding the number of lobes, the highest value recorded was in Tambo Grande, and the lowest value in Curimaná; regarding the length of the fruit, the highest value recorded was found in Oidor and the lowest in the population Yarinacocha. The Principal Component Analysis showed that 70.9% of the variance corresponds to the two first components. Groups clearly defined were not observed; however, the populations of the coastal region formed groups distinct from those of the jungle region. Keywords: piñon blanco, morfometric, variance analysis, principal components analysis.
Tesis
Jereissati, Camila Barbosa Pinheiro. "Proteomic analysis of plastids the endosperm of developing seeds of Jatropha (Jatropha curcas L.)." Universidade Federal do CearÃ, 2015. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=13786.
Full textJatropha curcas L. is a plant native to America and belongs to the Euphorbiaceae family. Currently it is gaining economical interest mainly because it is an oilseed crop with potential to produce biodiesel. However, presence of phorbol esters (a class of diterpenes) that are the major toxic constituents of the seeds, limits a better usage of the plant, by making the use of the residue, obtained after the oil extraction from the seeds, unfeasible for animal feed, due to its pro-carcinogenic activity and inflammatory action. Proteomic analysis of the plastids isolated from developing seeds of Jatropha is important because the synthesis of fatty acid as well as phorbol esters, the two most attractive compounds in the study of Jatropha curcas, occur in plastids. Proteomic analysis of this organelle is crucial to better understand and explore not only the biosynthetic pathway of these two compounds but other metabolic pathways , and addtionaly providing foundation for researchs that aimed to develope genotypes with more suitable characteristics for industrial applications. In this study, we performed a proteomic analysis of plastids isolated from the endosperm of developing Jatropha curcas seeds that were in the initial stage of deposition of protein and lipid reserves. Proteins extracted from the plastids were digested with trypsin, and the peptides were applied to an EASY-nano LC system coupled online to an ESI-LTQ-Orbitrap Velos mass spectrometer, and this led to the identification of 1103 proteins representing 804 protein groups, of which 923 were considered as true identifications, and this considerably expands the repertoire of J. curcas proteins identified so far. Of the identified proteins, only five are encoded in the plastid genome, and none of them are involved in photosynthesis, evidentiating the nonphotosynthetic nature of the isolated plastids. Homologues for 824 out of 923 identified proteins were present in three different plastids proteins databases i.e. PPDB, SUBA and PlProt, while homologues for 13 proteins were not found in any of these three databases but were marked as plastidial by at least one of the three prediction programs used (TargetP, ChloroP and PlantMPloc). Functional classification showed that proteins belonging to amino acids metabolism comprise the main functional class, followed by carbohydrate, energy, and lipid metabolisms. The small and large subunits of Rubisco were identified, and their presence in plastids is considered to be an adaptive feature counterbalancing for the loss of one-third of the carbon as CO2 as a result of the conversion of carbohydrate to oil through glycolysis. While several enzymes involved in the biosynthesis of several precursors of diterpenoids were identified, we were unable to identify any terpene synthase/cyclase, which suggests that the plastids isolated from the endosperm of developing seeds do not synthesize phorbol esters. In conclusion, this study provides insights into the major biosynthetic pathways and certain unique features of the plastids from the endosperm of developing seeds at the whole proteome level.
O pinhÃo manso (Jatropha curcas L.) à uma planta nativa da AmÃrica, pertencente à famÃlia Euphorbiaceae. Atualmente, ela desperta interesse econÃmico principalmente por se tratar de uma oleaginosa com potencial para a produÃÃo de biodiesel. Entretanto, a presenÃa de Ãsteres de forbol (uma classe de diterpeno), que sÃo os principais constituintes tÃxicos das sementes, limita uma melhor utilizaÃÃo dessa planta, por inviabilizar o uso do resÃduo de extraÃÃo do Ãleo das sementes na alimentaÃÃo animal, bem como, por apresentar atividade prÃ-carcinogÃnica e aÃÃo inflamatÃria. A anÃlise proteÃmica de plastÃdeos, isolados de sementes em desenvolvimento de pinhÃo manso, à uma importante vertente de estudo, pois tanto a sÃntese de Ãcidos graxos como dos Ãsteres de forbol, os dois compostos mais atrativos no estudo de Jatropha curcas, ocorrem nos plastÃdeos. O estudo proteÃmico dessa organela torna-se crucial para melhor compreender e explorar nÃo somente as vias biossintÃticas desses dois compostos, como de outras vias metabÃlicas, alÃm de proporcionar um conjunto de dados que pode ser utilizado em pesquisas voltadas para o desenvolvimento de genÃtipos com caracterÃsticas mais adequadas para aplicaÃÃes industriais. No presente trabalho, realizou-se uma anÃlise proteÃmica de plastÃdeos isolados do endosperma de sementes em desenvolvimento do pinhÃo manso, que estavam nos estÃgios iniciais de deposiÃÃo de lipÃdios e proteÃnas de reserva (25-30DAA), confirmados por meio de anÃlises histolÃgica e histoquÃmica. As proteÃnas extraÃdas dos plastÃdeos foram digeridas com tripsina e os peptÃdeos foram aplicados no sistema de nano-LC EASYII acoplado online ao espectrÃmetro de massa nano ESI LTQ-Orbitrap velos, o que resultou na identificaÃÃo 1103 proteÃnas, representando 804 grupos de proteÃnas, dos quais 923 foram consideradas identificaÃÃes verdadeiras. Isso expandiu consideravelmente o repertÃrio de proteÃnas do pinhÃo manso atà agora identificas. Dentre as proteÃnas identificadas, apenas 5 sÃo codificadas pelo genoma plastidial, e nenhuma delas està envolvida na fotossÃntese, o que evidencia a natureza nÃo fotossintÃtica dos plastÃdeos isolados. HomÃlogos de 824, dentre as 923 proteÃnas identificadas, estavam presentes nos bancos de dados PPDB, SUBA e PlProt, enquanto homÃlogos para 13 proteÃnas nÃo foram encontrados em nenhum dos trÃs bancos de dados plastidiais, mas foram detectados como plastidiais por pelo menos um dos trÃs programas de prediÃÃo de localizaÃÃo subcelular utilizados (TargetP, ChloroP, PlantMPloc). A classificaÃÃo funcional mostrou que a maioria das proteÃnas identificadas pertencia ao metabolismo dos aminoÃcidos, seguido dos metabolismos dos carboidratos, energÃtico e dos lipÃdios. As subunidades maiores e menores da Rubisco foram identificadas, e sua presenÃa nos plastÃdeos foi considerada uma caracterÃstica adaptativa para contrabalancear a perda de um terÃo do carbono na forma de CO2 como um resultado da conversÃo de carboidratos em Ãleo atravÃs da glicÃlise. Apesar de enzimas envolvidas na biossÃntese de diversos precursores dos diterpenÃides terem sido identificadas, nÃo foi detectado nenhuma terpeno sintase/ciclase, o que sugere que os plastÃdeos isolados do endosperma de sementes em desenvolvimento nÃo sintetizam Ãsteres de forbol, apesar de uma grande quantidade desse composto ser encontrada neste tecido. Como conclusÃo, o presente trabalho proporciona insights sobre as principais vias biossÃntÃticas, e sobre caracterÃsticas peculiares dos plastideos isolados do endosperma de sementes em desenvolvimento.
Kasim, Farizul Hafiz. "In situ transesterification of Jatropha curcas for biodiesel production." Thesis, University of Newcastle Upon Tyne, 2012. http://hdl.handle.net/10443/1788.
Full textDyer, Jennifer Clare. "Jatropha curcas as a livelihood diversification strategy in Malawi." Thesis, University of Leeds, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.589046.
Full textRibeiro, Sandra Santos. "Estudo fitoquímico e atividades biológicas de Jatropha curcas L." Universidade Federal de Sergipe, 2010. https://ri.ufs.br/handle/riufs/6059.
Full textIn this work was determined, for the first time, the volatile composition from fresh and dried leaves of six accessions (named PM-2, PM-7, PM-10, PM-11, PM-12 e PM-14) and a cultivar (EPAMIG, named here EMB) of Jatropha curcas L. The volatile compounds was extracted by hydrodistillation and then analyzed by GCMS. Thus, it was possible to observe that the (Z)-3-hexen-1-ol was the major compound in the fresh leaves (>70% in all accessions). Alcohols also predominated in the dried leaves, mainly (Z)-2-penten-1-ol and (Z)-3-hexen-1-ol, but others constituents were identified in significant proportions included benzenoid compounds such as benzaldehyde. The influence of drying on volatile composition from leaves of J. curcas was evaluated on the PM-2 accession. Besides, this work also describes the development of a High Performance Liquid Chromatograpy (HPLC) method for differentiation of six accessions and a cultivar (EPAMIG) from fresh and dried leaves of J. curcas. The methanol extracts of the leaves were analyzed by HPLC-DAD and after stages of optimizations, we obtained the fingerprint chromatograms. For a comparative analysis of the accessions and a cultivar, were applied chemometric tools of Principal Component Analysis (PCA) and Hierarchical Cluster Analysis (HCA), which it was possible to discriminate the samples from dried leaves according to their origins. The methanol extracts of the leaves were submitted to cytotoxicity assay against four tumor cell lines (HCT-8, HL-60, SF-295 and MDA-MB435), presenting IC50 values of 25.13 μg/ml, against HL-60 cell line for EMB sample considered promising by National Institute of Cancer, USA (NCI). The biological activity of this extracts was evaluated on the development of Spodoptera frugiperda, considered as a primary pest in corn crop. It was observed 60% larval mortality.
No presente trabalho foi determinado, pela primeira vez, os compostos voláteis das folhas frescas e secas de Jatropha curcas L. pela técnica de hidrodestilação, para seis diferentes acessos (denominados de PM-2, PM-7, PM-10, PM-11, PM- 12 e PM-14) e uma cultivar (EPAMIG, denominada de EMB). As análises foram realizadas através de CG/EM, obtendo-se o (Z)-3-hexen-1-ol (75,7±18,2%) como composto majoritário nas folhas frescas, com percentuais superiores a 70% entre os acessos. Nas folhas secas obteve-se como compostos majoritários o (Z)-2- penten-1-ol (14,9±11,3%), (Z)-3-hexen-1-ol (9,6±9,1%) e o benzaldeído (3,9±2,7%). Um experimento de secagem foi realizado para o acesso PM-2 com intuito de verificar o efeito da secagem na composição dos voláteis das folhas de J. curcas. Neste trabalho também foi desenvolvido um método por Cromatografia Líquida de Alta Eficiência (CLAE) para diferenciação dos seis acessos e da cultivar (EPAMIG) para folhas frescas e secas de J. curcas. Os extratos metanólicos das folhas foram analisados por CLAE-DAD e após etapas de otimizações, foram obtidos os cromatogramas fingerprints. Para uma análise comparativa entre os acessos e a cultivar, aplicaram-se ferramentas quimiométricas de Análise dos Componentes Principais (PCA) e Análise de Agrupamentos Hierárquicos (HCA), pelas quais foi possível diferenciar as amostras das folhas secas de acordo com suas procedências. Os extratos metanólicos também foram submetidos a ensaios de citotoxicidade in vitro para 04 linhagens de células tumorais humanas (HCT-8, HL-60, SF-295 e MDA-MB- 435), obtendo-se CI50 25,13 μg/mL, na linhagem HL-60 para a amostra da cultivar (EPAMIG). Este resultado está dentro do intervalo proposto pelo National Institute of Cancer, USA (NCI) para considerar extratos como promissores. A atividade biológica destes extratos também foi avaliada sobre o desenvolvimento de Spodoptera frugiperda, principal praga do milho, apresentando 60% de mortalidade larval.
Shah, Mohibullah. "Proteome analysis of developing seeds of Jatropha curcas L." Universidade Federal do CearÃ, 2014. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=11638.
Full textPhysic nut (Jatropha curcas L.) is an important crop due to its ability of storing high content of oil in the seeds, which can serve as raw material for biodiesel production. Because of the presence of toxic constituents like phorbol esters (PEs) and curcins, the seed cake produced as a result of oil extraction cannot be utilize for animal feed. Development of the genotypes better suited for the industrial applications and biodiesel production as well as with lower level of toxic constituents is being hampered by a lack of understanding about the a) proteins related to the biosynthesis and degradation of fatty acids (FAs) and triacylglycerides (TAGs), b) role of proteins deposited during seed development and c) proteins related to the synthesis and storage of toxic compounds during seed development. Agreeing with this, we have performed the anatomical analysis of the developing seeds of J. curcas, followed by the proteome analysis of the endosperm isolated from the seeds of J. curcas at five different developmental stages, which resulted into the identification of the 1517, 1256, 1033, 752 and 307 proteins, from Stage 6, 7, 8, 9 and 10, respectively, summing up to a total of 1760 proteins. Proteins with similar expression pattern were grouped into five different clusters and protein quantification based on spectral counts was determined. Besides identification of the proteins involved in the biosynthesis and degradation of the FAs and TAGs, we also identified a large number of proteins involved in the metabolism of the carbohydrates, which are important for supplying energy and carbon source for the synthesis of TAGs in heterotrophic seeds. Among the members of different classes of seed storage proteins (SSPs), we have identified four SSPs named as nutrients reservoir, which in contrast to the other SSPs showed decreasing deposition pattern during seeds development and revealed to have special role during seed development. In addition, peptidases belong to different mechanistic classes were identified, which have a range of functions, highlighting the role in reserve mobilization during germination. Isoforms of curcin were also identified in this proteome analysis which were absent in our previous proteome analysis of the other tissues from these seeds, suggesting that the deposition of these toxic proteins only occur in the endosperm. Similarly, several enzymes involved in the biosynthesis of diterpenoid precursors were identified in this proteome analysis but, like in our previous proteome analysis of the other tissues from J. curcas seeds,we were unable to identify any terpene synthase/cyclase, enzymes responsible for the synthesis of PEs, which collectively suggesting that the synthesis of PEs may not occur in seeds of this plant. In conclusion, the strategy used here enabled us to provide a first in depth proteome analysis of the endosperm from J. curcas developing seeds, which along with providing information regarding important aspects of the seed development, also set the foundation of a proteomic approach to study biotechnologically important plant species.
PinhÃo manso (Jatropha curcas L.) à uma cultura importante devido à sua habilidade em armazenar alto conteÃdo de Ãleo nas sementes, as quais podem servir como matÃria-prima para a produÃÃo de biodiesel. Devido à presenÃa de constituintes tÃxicos como Ãsteres de forbol e curcina, a torta da semente produzida como resultado da extraÃÃo do Ãleo nÃo pode ser utilizada na alimentaÃÃo animal. O desenvolvimento de genÃtipos mais adequados a aplicaÃÃes industriais e à produÃÃo de biodiesel assim como apresentando baixos nÃveis de constituintes tÃxicos està sendo prejudicado pela falta de entendimento sobre a) proteÃnas relacionadas a biossÃntese e degradaÃÃo de Ãcidos graxos e triacilglicerÃis, b) o papel de proteÃnas depositadas durante o desenvolvimento da semente e c) proteÃnas relacionadas à sÃntese e reserva de compostos tÃxicos durante o desenvolvimento da semente. Diante disso, nÃs realizamos uma anÃlise anatÃmica de sementes em desenvolvimento de J. curcas, seguido por uma anÃlise proteÃmica do endosperma isolado de sementes dessa espÃcie em cinco diferentes estÃgios de desenvolvimento, o que resultou na identificaÃÃo de 1517, 1256, 1033, 752 e 307 proteÃnas, dos estÃgios 6, 7, 8, 9 e 10, respectivamente, somando um total de 1760 proteÃnas. ProteÃnas com padrÃo de expressÃo similar foram agrupadas em cinco grupos diferentes e a quantificaÃÃo das proteÃnas baseada na contagem dos espectros foi determinada. AlÃm da identificaÃÃo das proteÃnas envolvidas na biossÃntese e degradaÃÃo de FAs e TAGs, nÃs identificamos um grande nÃmero de proteÃnas envolvidas no metabolismo de carboidratos, as quais sÃo importantes para o fornecimento de energia e fontes de carbono para a sÃntese de TAGs em sementes heterotrÃficas. Entre os membros de diferentes classes de proteÃnas de reservas de sementes (SSPs), nÃs identificamos quatro SSPs denominadas reservatÃrios de sementes, que em contraste as outras SSPs mostraram decrÃscimo no padrÃo de deposiÃÃo e revelaram ter um papel especial durante o desenvolvimento da semente. Em adiÃÃo, peptidases pertencentes a diferentes classes mecanÃsticas foram identificadas destacando o papel da mobilizaÃÃo de reservas durante a germinaÃÃo. Isoformas da curcina ausentes em nossas anÃlises proteÃmicas prÃvias de outros tecidos da semente foram identificadas sugerindo que a deposiÃÃo dessas proteÃnas tÃxicas sà ocorre no endosperma. Similarmente, vÃrias enzimas envolvidas na biosÃntese de precursores de diterpenÃides foram identificadas nessa anÃlise proteÃmica, mas como em nossas prÃvias anÃlises proteÃmicas de outros tecidos de sementes de J. curcas, nÃs nÃo fomos capazes de identificar sintases/ciclases de terpenos, enzimas responsÃveis pela sÃntese de PEs, o que coletivamente sugere que a sÃntese desses compostos pode nÃo ocorrer nas sementes dessa planta. Em conclusÃo, a estratÃgia utilizada nos fornece a primeira anÃlise proteÃmica profunda do endosperma de sementes em desenvolvimento de J. curcas, o que alÃm de fornecer informaÃÃes sobre aspectos importantes do desenvolvimento da semente, tambÃm estabelece a base para uma pesquisa proteÃmica com o objetivo de estudar espÃcies vegetais importantes biotecnologicamente.
Moreira, Erica Rodrigues [UNESP]. "Métodos de propagação do pinhão manso (Jatropha curcas L.)." Universidade Estadual Paulista (UNESP), 2013. http://hdl.handle.net/11449/106164.
Full textA propagação do pinhão manso pode ser realizada via semente e vegetativa através de estacas e micropropagação. Quando realizada via semente, as plantas são mais vigorosas, porém iniciam a produção tardiamente. Utilizando-se estacas têm-se uma produção precoce e mantém as características da planta mãe, no entanto, verifica-se menor crescimento vegetativo inicial. Já a técnica da micropropagação pode produzir mudas sadias, em escala comercial com um curto período. Com isso objetivou-se com esta pesquisa, desenvolver protocolos para a propagação do pinhão manso via sementes, estaquia e micropropagação, visando à obtenção de mudas de qualidades. O projeto foi dividido em três partes: a primeira parte objetivou-se produzir plantas através de sementes, onde foram realizados testes pré-germinativos em diferentes substratos (comercial, vermiculita, areia); a segunda parte utilizou-se estacas, onde foram testadas partes do ramo (apical, mediana, basal) e diferentes substratos (comercial Bioplant®, vermiculita, areia) em duas épocas, agosto/2011 e março/2012. Na terceira parte foram desenvolvidas técnicas de micropropagação, envolvendo as etapas de assepsia dos explantes in vitro através do controle de contaminação utilizando concentrações de cloro ativo e tempo de imersão, problemas frequentes que inviabilizam a utilização da micropropagação para espécies lenhosas, como o pinhão manso; etapa de desenvolvimento onde estudou concentrações da citocinina 6-Benzilaminopurina (BAP) e dos sais do meio de cultivo Murashige e Skoog (1962) (MS); e a fase de enraizamento in vitro utilizando concentrações do ácido indol butírico (AIB). Concluiu-se que na propagação por sementes o melhor tratamento pré-germinativo foi a escarificação mecânica + imersão em água por 12 horas, e o uso do...
The propagation of physic nut can be realized by seed, vegetative by cuttings and micropropagation. When performed by seed, plants are more vigorous but begin production late. Using cuttings have an early production and keeps the characteristics of the parent plant, however, there is less initial vegetative growth. Since the technique of micropropagation can produce healthy seedlings in commercial scala with a short period. Therefore, objective was the research, develop protocols for the propagation of physic nut seeds, cuttings and micropropagation, in order to obtain seedlings qualities. The project was divided into three parts: the first part the objective was to produce plants by seed, where tests were performed pre-germination on different substrates (commercial, vermiculite, sand), the second part was used cuttings, where they were tested parts of the branch (apical, middle, basal) and different substrates (commercial, vermiculite, sand) in two seasons, from August/2011 and March/2012. In the third part have been developed of micropropagation techniques, involving the stages of aseptic explants in vitro through contamination control using ative chloro concentrations and time of immersion, frequent problems that hinder the use of micropropagation for woody species, like physic nut, development studying concentrations of cytokinin 6-benzylaminopurine (BAP) and salts of Murashige e Skoog (1962) (MS) medium and in vitro rooting concentrations of auxin indol butyric acid (IBA). It was concluded that the best seed propagation pre-germinative treatment was mechanical scarification + immersion in water for 12 hours, and the use of commercial substrate and vermiculite when using the cuttings the best time for propagation was August, and cuttings from the basal portion of the substrates and the use vermiculite and... (Complete abstract click electronic access below)
Moreira, Erica Rodrigues. "Métodos de propagação do pinhão manso (Jatropha curcas L.) /." Ilha Solteira, 2013. http://hdl.handle.net/11449/106164.
Full textBanca: Luiz de Souza Corrêa
Banca: Enes Furlani Junior
Banca: Enio Tiago de Oliveira
Banca: Flavia Dionisio Pereira
Resumo: A propagação do pinhão manso pode ser realizada via semente e vegetativa através de estacas e micropropagação. Quando realizada via semente, as plantas são mais vigorosas, porém iniciam a produção tardiamente. Utilizando-se estacas têm-se uma produção precoce e mantém as características da planta mãe, no entanto, verifica-se menor crescimento vegetativo inicial. Já a técnica da micropropagação pode produzir mudas sadias, em escala comercial com um curto período. Com isso objetivou-se com esta pesquisa, desenvolver protocolos para a propagação do pinhão manso via sementes, estaquia e micropropagação, visando à obtenção de mudas de qualidades. O projeto foi dividido em três partes: a primeira parte objetivou-se produzir plantas através de sementes, onde foram realizados testes pré-germinativos em diferentes substratos (comercial, vermiculita, areia); a segunda parte utilizou-se estacas, onde foram testadas partes do ramo (apical, mediana, basal) e diferentes substratos (comercial Bioplant®, vermiculita, areia) em duas épocas, agosto/2011 e março/2012. Na terceira parte foram desenvolvidas técnicas de micropropagação, envolvendo as etapas de assepsia dos explantes in vitro através do controle de contaminação utilizando concentrações de cloro ativo e tempo de imersão, problemas frequentes que inviabilizam a utilização da micropropagação para espécies lenhosas, como o pinhão manso; etapa de desenvolvimento onde estudou concentrações da citocinina 6-Benzilaminopurina (BAP) e dos sais do meio de cultivo Murashige e Skoog (1962) (MS); e a fase de enraizamento in vitro utilizando concentrações do ácido indol butírico (AIB). Concluiu-se que na propagação por sementes o melhor tratamento pré-germinativo foi a escarificação mecânica + imersão em água por 12 horas, e o uso do... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: The propagation of physic nut can be realized by seed, vegetative by cuttings and micropropagation. When performed by seed, plants are more vigorous but begin production late. Using cuttings have an early production and keeps the characteristics of the parent plant, however, there is less initial vegetative growth. Since the technique of micropropagation can produce healthy seedlings in commercial scala with a short period. Therefore, objective was the research, develop protocols for the propagation of physic nut seeds, cuttings and micropropagation, in order to obtain seedlings qualities. The project was divided into three parts: the first part the objective was to produce plants by seed, where tests were performed pre-germination on different substrates (commercial, vermiculite, sand), the second part was used cuttings, where they were tested parts of the branch (apical, middle, basal) and different substrates (commercial, vermiculite, sand) in two seasons, from August/2011 and March/2012. In the third part have been developed of micropropagation techniques, involving the stages of aseptic explants in vitro through contamination control using ative chloro concentrations and time of immersion, frequent problems that hinder the use of micropropagation for woody species, like physic nut, development studying concentrations of cytokinin 6-benzylaminopurine (BAP) and salts of Murashige e Skoog (1962) (MS) medium and in vitro rooting concentrations of auxin indol butyric acid (IBA). It was concluded that the best seed propagation pre-germinative treatment was mechanical scarification + immersion in water for 12 hours, and the use of commercial substrate and vermiculite when using the cuttings the best time for propagation was August, and cuttings from the basal portion of the substrates and the use vermiculite and... (Complete abstract click electronic access below)
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Books on the topic "Jatropha curcas"
Mohammad, Arif. Bio-diesel: Jatropha curcas (a promising source). Delhi, India: Satish Serial Pub. House, 2009.
Find full textJones, Norman. Jatropha curcas: A multipurpose species for problematic sites. [S.l.]: World Bank, Asia Technical Dept., Agriculture Division, 1991.
Find full textJones, Norman. Jatropha curcas: A multipurpose species for problematic sites. Washington, D.C: World Bank, Asia Technical Dept., Agriculture Division, 1991.
Find full textPengusaha Kecil dan Menengah. Deputi Bidang Produksi Indonesia. Departemen Koperasi. Budidaya dan pengolahan jarak pagar (Jatropha Curcas Linn). [Jakarta]: Deputi Bidang Produksi, Kementerian Negara Koperasi dan UKM, 2009.
Find full textNyamai, D. O. Jatropha curcas: The untapped potential in eastern and central Africa : production and utilization manual. Nairobi: Trees on-Farm Network, 2007.
Find full textPonterio, Claude. Jatropha curcas as a premier biofuel: Cost, growing and management. New York: Nova Science Publishers, 2010.
Find full textHeller, Joachim. Untersuchungen über genotpische Eigenschaften und Vermehrungs- und Anbauverfahren bei der Purgiernuss (Jatropha curcas L.). Hamburg: Dr. Kovač, 1992.
Find full textPrihandana, Rama. Integrated utilization of jatropha curcas: Road to energy self sufficient villages. Jakarta]: National Team for Biofuel Development for Accelerating Poverty Alleviation and Job Creation, 2007.
Find full textPrana, Made Sri. Budi daya jarak pagar (Jatropha curcas L.): Sumber biodiesel : menunjang ketahanan energi nasional. Jakarta: Lembaga Ilmu Pengetahuan Indonesia, Pusat Penelitian Bioteknologi, 2006.
Find full textMwamba, C. K. Photo-documentation on the promotion of soap and fuel production from Jatropha Curcas oil. Lusaka, Zambia: National Institute for Scientific and Industrial Research, 2002.
Find full textBook chapters on the topic "Jatropha curcas"
Ross, Ivan A. "Jatropha curcas." In Medicinal Plants of the World, 277–88. Totowa, NJ: Humana Press, 2003. http://dx.doi.org/10.1007/978-1-59259-365-1_14.
Full textMaravi, Devendra Kumar, Purabi Mazumdar, Shamsher Alam, Vaibhav V. Goud, and Lingaraj Sahoo. "Jatropha (Jatropha curcas L.)." In Methods in Molecular Biology, 25–35. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1658-0_3.
Full textKrist, Sabine. "Jatropha-Curcas-Samenöl." In Lexikon der pflanzlichen Fette und Öle, 279–83. Vienna: Springer Vienna, 2012. http://dx.doi.org/10.1007/978-3-7091-1005-8_42.
Full textKhare, C. P. "Jatropha curcas Linn." In Indian Medicinal Plants, 1. New York, NY: Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-70638-2_832.
Full textTomar, Nisha Singh, Mohammad Abass Ahanger, and R. M. Agarwal. "Jatropha curcas: An Overview." In Physiological Mechanisms and Adaptation Strategies in Plants Under Changing Environment, 361–83. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8600-8_13.
Full textSubedi, Chandra Kanta, Ram Prasad Chaudhary, Ripu M. Kunwar, Rainer W. Bussmann, and Narel Y. Paniagua-Zambrana. "Jatropha curcas L. Euphorbiaceae." In Ethnobotany of the Himalayas, 1111–21. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-57408-6_131.
Full textPaniagua-Zambrana, Narel Y., Rainer W. Bussmann, and Carolina Romero. "Jatropha curcas L. Jatropha gossypifolia L. Jatropha multifida L. Euphorbiaceae." In Ethnobotany of Mountain Regions, 1007–15. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-28933-1_154.
Full textPaniagua-Zambrana, Narel Y., Rainer W. Bussmann, and Carolina Romero. "Jatropha curcas L. Jatropha gossypifolia L. Jatropha multifida L. Euphorbiaceae." In Ethnobotany of Mountain Regions, 1–9. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-319-77093-2_154-1.
Full textMendonça, Simone, Taísa Godoy Gomes, Félix Gonçalves de Siqueira, and Robert Neil Gerard Miller. "Applications of Jatropha curcas Cake." In Jatropha, Challenges for a New Energy Crop, 365–80. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3104-6_18.
Full textMaghuly, Fatemeh, Gorji Marzban, Ebrahim Razzazi-Fazeli, and Margit Laimer. "Proteome Analyses of Jatropha curcas." In Biotechnologies for Plant Mutation Breeding, 203–23. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-45021-6_13.
Full textConference papers on the topic "Jatropha curcas"
Kumar, R., M. Sharma, S. S. Ray, A. S. Sarpal, A. A. Gupta, D. K. Tull, R. Sarin, R. P. Verma, and N. R. Raje. "Biodiesel From Jatropha curcas and Pongamia Pinnata." In SIAT 2004. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2004. http://dx.doi.org/10.4271/2004-28-0087.
Full textKelkar, Kshitij, Cibi selvam Mathialaghan, and Kamalkishore vora. "Process Parameter for Biodiesel Production - Jatropha Curcas." In 8th SAEINDIA International Mobility Conference & Exposition and Commercial Vehicle Engineering Congress 2013 (SIMCOMVEC). 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2013. http://dx.doi.org/10.4271/2013-01-2890.
Full textSrinophakun, Penjit, Anna Saimaneerat, Isara Sooksathan, Niphon Visarathanon, Savitree Malaipan, Kosol Charernsom, and Wiboon Chongrattanameteekul. "Integrated Research on Jatropha Curcas Plantation Management." In World Renewable Energy Congress – Sweden, 8–13 May, 2011, Linköping, Sweden. Linköping University Electronic Press, 2011. http://dx.doi.org/10.3384/ecp11057232.
Full textDasumiati, Dr, Mr Miftahudin, Ms Triadiati, and Hartana A. "Morphological and Growth Characters ofnAndromonoecious Jatropha curcas." In International Conference on Science and Technology (ICOSAT 2017) - Promoting Sustainable Agriculture, Food Security, Energy, and Environment Through Science and Technology for Development. Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/icosat-17.2018.29.
Full textSaragih, Triando Hamonangan, Diny Melsye Nurul Fajri, Andi Hamdianah, Wayan Firdaus Mahmudy, and Yusuf Priyo Anggodo. "Jatropha curcas disease identification using Fuzzy Neural Network." In 2017 International Conference on Sustainable Information Engineering and Technology (SIET). IEEE, 2017. http://dx.doi.org/10.1109/siet.2017.8304153.
Full textKhan, M. Bilal, Ali Bahadar, Waqas Anjum, L. T. Handoko, and Masbah R. T. Siregar. "Production of Biodiesel from Jatropha Curcas using Nano Materials." In INTERNATIONAL WORKSHOP ON ADVANCED MATERIAL FOR NEW AND RENEWABLE ENERGY. AIP, 2009. http://dx.doi.org/10.1063/1.3243252.
Full textEffendi, Z., R. Ramli, J. A. Ghani, and M. N. A. Rahman. "Pattern recognition system of Jatropha curcas fruits using back propagation." In 2009 IEEE International Conference on Signal and Image Processing Applications. IEEE, 2009. http://dx.doi.org/10.1109/icsipa.2009.5478719.
Full textFajri, Diny Melsye Nurul, Triando Hamonangan Saragih, Andi Hamdianah, Wayan Firdaus Mahmudy, and Yusuf Priyo Anggodo. "Optimized fuzzy neural network for Jatropha Curcas plant disease identification." In 2017 International Conference on Sustainable Information Engineering and Technology (SIET). IEEE, 2017. http://dx.doi.org/10.1109/siet.2017.8304152.
Full textGOUVEIA, A. de F., P. D. MACRUZ, and J. H. B. de ARAÚJO. "FITORREMEDIAÇÃO DE SOLOS CONTAMINADOS COM CHUMBO UTILIZANDO Jatropha curcas L." In XX Congresso Brasileiro de Engenharia Química. São Paulo: Editora Edgard Blücher, 2015. http://dx.doi.org/10.5151/chemeng-cobeq2014-1105-20957-149786.
Full textDiotto, A. V., T. L. Romanelli, J. P. Francisco, B. P. Lena, and M. V. Folegatti. "Energy Embodiment in Irrigation Systems of Physic Nut (Jatropha curcas L.)." In II Inovagri International Meeting. Fortaleza, Ceará, Brasil: INOVAGRI/INCT-EI/INCTSal, 2014. http://dx.doi.org/10.12702/ii.inovagri.2014-a257.
Full textReports on the topic "Jatropha curcas"
Wahl, N, N., R. Jamnadass, H. Baur, C. Munster, and M. Iiyama. Economic viability of Jatropha curcas L. plantations in Northern Tanzania ICRAF Working paper no. 97. World Agroforestry Centre (ICRAF), 2009. http://dx.doi.org/10.5716/wp16542.pdf.
Full textGhosh, Arup, Jitendra Chikara, and Candace Wheeler. Determination of the Economic Viability & Technical Feasibility of Commercial Jatropha Curcas Production for Generation of Jatropha oil as Bio-Fuel Feedstock from Wasteland: Final Technical Report on Life Cycle Impact Assessment of Jatropha Cultivation. Office of Scientific and Technical Information (OSTI), December 2012. http://dx.doi.org/10.2172/1320736.
Full textTomomatsu, Y., and B. Swallow. Jatropha curcas biodiesel production in Kenya: economics and potential value chain development for smallholder farmers ICRAF Working Paper no. 54. World Agroforestry Centre (ICRAF), 2007. http://dx.doi.org/10.5716/wp15396.pdf.
Full textWeyerhaeuser, H., T. Tennigkeit, S. Yufang, and F. Kahrl. Biofuels in China: an analysis of the opportunities and challenges of Jatropha curcas in Southwest China ICRAF Working Paper no. 53. World Agroforestry Centre (ICRAF), 2007. http://dx.doi.org/10.5716/wp07259.pdf.
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