Submitted by Edisangela Bastos (edisangela@ufpa.br) on 2018-09-14T17:56:45Z No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_EssentialOilsComponents.pdf: 4263439 bytes, checksum: c1189e55f12d63ca94f4a519200746ce (MD5) / Approved for entry into archive by Edisangela Bastos (edisangela@ufpa.br) on 2018-09-14T17:57:50Z (GMT) No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_EssentialOilsComponents.pdf: 4263439 bytes, checksum: c1189e55f12d63ca94f4a519200746ce (MD5) / Made available in DSpace on 2018-09-14T17:57:50Z (GMT). No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Tese_EssentialOilsComponents.pdf: 4263439 bytes, checksum: c1189e55f12d63ca94f4a519200746ce (MD5) Previous issue date: 2017-03-31 / Óleos essenciais derivados do metabolismo secundário de plantas podem ter atividades contra nematóides das galhas, Melodogyne incognita. Devido à necessidade de nematicidas mais eficientes e menos tóxicos para o homem e para o ambiente do que os disponíveis para o controle de Meloidogyne incognita, assim, neste trabalho objetivou-se estudar os óleos essenciais de Cinnamomum cassia e de Allium sativum, que foram descritos como ativos in vitro contra o nematóide Bursaphelenchus xylophilus. O óleo essencial de ambas as espécies foi obtido por hidrodestilação, dissolvidos em solução aquosa de Tween 80 a 0,01 g mL-1 e testado in vitro contra M. incognita. A 62 μg mL-1 as emulsões dos óleos foram mais ativas sobre ovos e juvenis de segundo estagio (J2) do que o Carbofuran a 173 μg mL-1. De acordo com a análise de cromatografia gasosa-espectrometria de massas, o constituinte majoritário de C. cassia é o (E)-cinamaldeído (83,3%), enquanto para o óleo de alho foram trisulfeto de dialila (66.7%) e dissulfeto de dialila (21.3%). Esses constituintes explicaram a atividade nematicida in vitro do óleo essencial de cada espécie de planta. A emulsão do óleo de C. cassia (500 μg mL-1), (E)-cinamaldeído (416 μg mL-1) e alho (250 μg mL-1) reduziram o numero de galhas e de ovos em plantas de soja e tomateiro, respectivamente, a valores estatisticamente iguais àquele obtido pelo Carbofuran (416 μg mL-1). Vapores dos óleos essenciais e do (E)-cinamaldeído foram ativos tanto quanto o nematicida fumigante Basamid usado nos ensaios in vitro contra M. incognita. A infectividade e a reprodução de M. incognita em plantas de soja e de tomate cultivadas em substrato infestado artificialmente com ovos do nematóide e tratado com 0,2 mL (alho), 1,0 mL (E)-cinamaldeído e 0,25 g de Basamid foram estatisiticamente iguais entre si na redução da população do nematoide. Esses resultados inequivocamente provam a atividade nematicida dos óleos essenciais e da substância (E)-cinamaldeído contra M. incognita, portanto, tanto o óleo quanto o (E)-cinamaldeído são muito promissores ao desenvolvimento de novos nematicidas fumigantes para o controle de nematóides em plantas de soja e de tomate. / Essential oils derived from secondary plant metabolism may have activities against root-knot nematodes, Meloidogyne incognita. Because nematicides that are more efficient and less toxic to humans and the environment than those available are desirable to control this pathogen, this work aimed at studying the essential oil of Cinnamomum cassia and Allium sativum, which were described as active in vitro against the nematode Bursaphelenchus xylophilus. The essential oils of both species were obtained by hydrodistillation, initially dissolved in aqueous solution of Tween 80 at 0.01 g mL-1 and tested in vitro against M. incognita. At 62 μg mL-1 the oil emulsions were more active on eggs and second stage juveniles (J2) than Carbofuran at 173 μg mL-1. According to gas chromatography-mass spectrometry analysis, the major constituent of C. cassia is (E) -cinnamaldehyde (83.3%), while for garlic oil were diallyl trisulfide (66.7%) and diallyl disulfide (21.3%). These constituents explained the in vitro nematicidal activity of the essential oil of each plant species. The emulsion of the C. cassia (500 μg mL-1), E)-cinnamaldehyde (416 μg mL-1) and garlic (250 μg mL -1) reduced the number of galls and eggs in roots soybean and tomatoes to values statistically equal to those obtained with Carbofuran at 415 μg mL-1. Vapors from the essential oils and (E)-cinnamaldehyde were active as much as the basamid fumigant nematicide used in the in vitro assays against M. incognita. Infectivity and reproduction of M. incognita in soybean and tomato plants grown on substrate artificially infested with nematode eggs and treated with 0.2 mL (garlic), 1.0 mL (E)-cinnamaldehyde and 0.25 g of Basamid were statistically equal among themselves in reducing the nematode population. These results unequivocally proofs of the nematicidal activity of the essential oils and of the (E)-cinnamaldehyde substance against M. incognita, therefore, both oil (E)-cinnamaldehyde are very promising to the development of new fumigant nematicides for the control of nematodes in soybean and tomato plants. / UFPA/Altamira

Submitted by (lucia.rodrigues@ufrpe.br) on 2017-02-21T14:29:54Z No. of bitstreams: 1 Daniela Silva Salgues de Matos.pdf: 1116050 bytes, checksum: 68451ef17c78b83ff4481e7a8cf6826c (MD5) / Made available in DSpace on 2017-02-21T14:29:54Z (GMT). No. of bitstreams: 1 Daniela Silva Salgues de Matos.pdf: 1116050 bytes, checksum: 68451ef17c78b83ff4481e7a8cf6826c (MD5) Previous issue date: 2010-02-22 / Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPq / In Northeastern Brazil the root-knot (Meloidogyne spp.) and lesion (Pratylenchus zeae) nematodes are important plant pathogens in sugarcane growing areas, causing damage higher than 20% of production. Several control measures are recommended for nematode control, however none of them is effective enough in decreasing initial population density and avoiding environmental risks. Adequate sampling would improve nematode management and reduce costs. On the other hand, the vinasse application has been frequently emphasize because of the high residue amount from sugarcane industrialization and high pollution from excessive oxygen demand. The objectives of the present study were to evaluate in costal table and lean areas effects of the sugarcane irrigation with vinasse on nematode communities and chemical atributes of soil, correlating effects among variables analyzed and sampling net; indicate sample number for monitoring Meloidogyne spp. and P. zeae and characterize the spatial variability of these nematodes in costal table irrigated with vinasse. The experiments were carried out in costal table and lean areas cultivated with sugarcane irrigated and non irrigated with vinasse. Soil samples were collected 25-cm deep in 1×1, 10×10 and 50×50-m square net samplings, with 36 points each, in a total area of 25 m2, 2,500 m2 and 62,500 m2, respectively. Techniques of descriptive statistics and geostatistics were applied for characterize the magnitude of spatial dependence of nematode distribution.In order to provide data for an adequate disease management in the area, it was drawn krigagen maps of nematodes spatial distribution. In general, nematode population dynamic depended on vinasse application and chemical characteristics of the soil. In coastal tables, phosphorus, calcium and cation concentration significantly correlated with plant parasite nematodes (r = -0.17, 0.17 and 0.16) and total nematodes (r = -0.20, 0.21, 0.17), respectively. In lean lands there was negative correlation between magnesium and plant parasitic nematodes (r = -0.16). Total amount of nematode in irrigated area was lower than in non irrigated one. Ten up to 75 and 12 up to 40 soil and root samples, respectively, were indicated for monitoring P. zeae depending on sampling net. For Meloidogyne spp. the number of samples ranged from 34 to 132 and 13 to 117 for soil and root, respectively, depending on sampling net. According to semivariograms, Meloidogyne spp. presented moderate and strong spatial dependence in 1×1 and 50×50-m net, respectively, and P. zeae moderate spatial dependence in both nets. The Gaussian model best fitted Meloidogyne spp. in 1×1-m net and P. zeae in both 1×1 and 50×50-m net. For Meloidogyne spp. in 50×50-m net the exponential model fitted the best. In 10×10-m net there was pure nugget effect model for both nematodes. / No Nordeste brasileiro os nematóides das galhas (Meloidogyne spp.) e das lesões (Pratylenchus zeae) são importantes patógenos da cana-de-açúcar, causando danos superiores a 20% na produção. Diversas medidas para controle de nematóides são recomendadas, porém nenhuma tem se mostrado efetiva em reduzir as populações iniciais e evitar riscos ambientais. A coleta adequada de amostras para análise nematológica pode permitir adoção de práticas eficientes e com menores custos no controle desses patógenos. Por outro lado, a aplicação de vinhaça tem sido bastante enfatizada, em razão da elevada quantidade gerada pelas usinas e destilarias, e por ser considerada altamente poluente devido à alta demanda de oxigênio. Os objetivos do presente estudo foram avaliar em áreas de encosta e tabuleiro efeitos da fertirrigação da cana-de-açúcar com vinhaça nas comunidades de nematóides e atributos químicos do solo relacionando efeitos entre as variáveis analisadas e malha de amostragem; recomendar número de amostras para monitoramento de Meloidogyne spp. e P. zeae; e caracterizar a variabilidade espacial destes fitoparasitos em tabuleiro irrigado com vinhaça. Os experimentos foram conduzidos em áreas de tabuleiro e de encosta cultivadas com cana-de-açúcar com e sem aplicação de vinhaça. Amostras de solo e de raiz foram coletadas a 25 cm de profundidade e em cada área foi estabelecida malhas de amostragem quadrangular de 1×1; 10×10 e 50×50 m, com 36 pontos cada, totalizando áreas de 25 m2, 2.500 m2 e 62.500 m2, respectivamente. Técnicas de estatística descritiva e geoestatística foram empregadas para caracterização da magnitude da dependência espacial da distribuição dos nematóides. Com finalidade de fornecer subsídios para um manejo mais adequado da doença na área estudada, foram confeccionados mapas de krigagem da distribuição dos nematóides. De maneira geral, a dinâmica populacional dos nematóides foi dependente das características químicas do solo e da aplicação de vinhaça. Nas áreas de tabuleiro, o fósforo, o cálcio e a saturação de bases correlacionaram-se significativamente com fitoparasitos (r = -0,17; 0,17 e 0,16) e com total de nematóides (r = -0,20; 0,21 e 0,17), respectivamente. Na área de encosta, foi detectada correlação negativa entre magnésio e os fitoparasitos (r = -0,16). O total de nematóides na área irrigada foi menor do que na área não irrigada. Dez a 75 amostras de solo e 12 a 40 amostras de raiz por área foram indicadas para monitoramento de P. zeae variando de acordo com a malha de amostragem adotada.Para Meloidogyne spp. o número de amostras variou de 34 a 132 e de 13 a 117 para solo e raiz, respectivamente, dependendo da malha amostrada. Os semivariogramas experimentais indicaram dependência espacial moderada e forte para Meloidogyne spp. de 1×1 e 50×50 m, respectivamente, e moderada para P. zeae nas duas malhas. O modelo Gaussiano proporcionou melhor ajuste do semivariograma experimental para Meloidogyne spp. na malha de 1×1 m e P. zeae nas malhas de 1×1 e 50×50 m. Para Meloidogyne spp. na malha de 50×50 m o modelo que melhor se ajustou foi o Exponencial. Na malha de 10×10 m ocorreu efeito pepita puro para ambos os nematóides.

Thesis (M. Agricultural Management (Animal Production)) -- University of Limpopo, 2016 / Cultivated potato (Solanum tuberosum L.) cultigens do not have resistant genotypes to root-knot (Meloidogyne species) nematodes. Currently, efforts are underway to introgress nematode resistance in potato breeding programmes, whereas other environment-friendly nematode management strategies are being assessed in various cultigens. Nemafric-BL and Nemarioc-AL phytonematicides have being researched and developed for managing the root-knot nematode whereas Biocult Mycorrhizae are intended to enhance crop productivity through improved absorption of P, which is inherently low in most South African soils. The objectives of the study, therefore, were: (1) to determine the interactive effects of Nemacur (N), Biocult Mycorrhizae (B) and Nemarioc-AL or Nemafric-BL phytonematicide (P) on population densities of M. javanica and growth of potato plants, (2) to investigate the effects of Nemacur (N), Velum (V), Biocult Mycorhizae (B) and Nemarioc-AL or Nemafric-BL phytonematicide (P) on population densities of M. javanica and growth of potato plants. For the microplot experiment, potato cv. ‘Mondial G3’ seeds were sown in 25 cm-diameter plastic pots with 5 000 ml steam-pasteurised river sand and Hygromix-T at 3:1 (v/v) growing mixture in autumn (March-May) 2015. Pots were buried 80% deep into the soil in with 0.5 m inter-row and 0.5 m intra-row spacing. Potato cv. ‘Mondial G3’ seeds were dipped in a mixture of Mancozeb with a wettener for disease management prior to sowing. Appropriate treatments were applied soon after emergence of leaves. Each plant was inoculated by dispensing a mixture of 5 000 eggs and M. javanica J2. Eight treatments, control (N0B0P0), Nemacur (N1B0P0), Biocult (N0B1P0), phytonematicide (N0B0P1), Nemacur × Biocult (N1B1P0), Nemacur × phytonematicide (N1B0P1), Biocult × phytonematicide (N0B1P1) and Nemacur × Biocult × phytonematicide (N1B1P1), were arranged in a randomised complete block xxvi design (RCBD) with 8 replications (n= 64). Under field conditions the study was conducted in summer (October 2015 - January 2016), with 30-cm furrows dug and potato seeds placed in the soil with 30 cm inter-row and 40 cm intra-row spacing. The four treatments, namely, (1) untreated control, (2) Nemacur or Velum (3) Biocult Mycorrhizae and (4) Nemarioc-AL or Nemafric-BL phytonematicide, were arranged in RCBD, replicated three times for the Velum experiment and five times for the Nemacur experiment. At 56 days after inoculation, the second order interaction (N1B1P1) was highly significant (P ≤ 0.01) for eggs in root and total nematodes, contributing 13 and 12% to total treatment variation (TTV) of the two variables, respectively, in the Nemarioc-AL phytonematicide study. Relative to untreated control, the second order interaction (N1B1P1) reduced eggs in root and total nematodes by 42 and 36%, respectively. In both Nemarioc-AL and Nemafric-BL phytonematicide experiments, the combination of phytonematicide and Biocult Mycorrhizae reduced gall rating. Nemacur, Biocult and Nemarioc-AL phytonematicide, the treatment effects were highly significant on eggs, J2 in root and total nematodes, contributing 53, 68 and 57% to TTV of the three variables, respectively. Nemacur, Biocult and Nemafric-BL phytonematicide treatments each was not significant (P ≤ 0.05) for nematodes variables. Both treatments for Nemacur, Biocult and Nemarioc-AL or Nemafric-BL phytonematicides were significant for gall rating, contributing 92 and 70% to TTV of the variable, respectively. In Nemarioc-AL phytonematicide, relative to the untreated control, gall rating was reduced by 48 to 56%, whereas in Nemafric-BL phytonematicide the variable was reduced by 33 to 56%. In the Velum study, Biocult and Nemarioc-AL or Nemafric-BL phytonematicide, the treatment effects in both experiments were highly significant (P ≤ 0.01) on eggs in root, contributing 88% to TTV of the variable. Both treatments from Nemarioc-AL xxvii and Nemafric-BL phytonematicides had no significant effects on all plant variables measured. In microplot, the second order interaction (Nemacur × Biocult × Nemarioc-AL phytonematicide) was highly significant for nematode eggs in root and total nematode. In a three-way matrix, the N1B1P1 interaction had the highest effects on eggs, followed by Biocult alone, then Nemacur alone and then the phytonematicide. The same trend was observed in the three-way matrix for total nematodes. However, in two-way matrix for eggs, Biocult outperformed Nemacur, as was the phytonematicide on J2. In another microplot study, the second order interaction (Nemacur × Biocult × Nemafric-BL phytonematicide) was significant for J2 in soil and roots, with the three-way matrix showing, that Biocult alone had higher effects than the N1B1P1 interaction on J2 in root. A three-way matrix also showed that Nemacur was outperformed by the phytonematicide alone, Biocult alone and the interactions on J2 in soil. In conclusion, Nemarioc-AL and Nemafric-BL phytonematicides could each be used with Biocult Mycorrhizae in the management of population densities of M. javanica in potato production since the impact from Nemacur which is a synthetic nematicide does not have that much difference from that of phytonematicides interacted with Biocult Mycorrhizae. / Agricultural Research Council

Thesis (M.A. (Horticulture)) --University of Limpopo, 2010 / Refer to document / University of Namibia

Se determinó la respuesta de resistencia de 10 patrones de tomate a una población avirulenta de Meloidogyne javanica en maceta. Los ensayos se realizaron en primavera, cuando las temperaturas permitían la expresión fenotípica de la resistencia del gen Mi-1 (28˚C), en verano sometidos a altas temperaturas y en campo, exponiéndolos a altas densidades poblacionales del nematodo. A temperaturas inferiores a 28˚C los patrones mostraron gran variabilidad en la respuesta de resistencia que osciló entre alta y moderadamente resistente (PG-76, Gladiator, MKT-410; Brigeor, 42851, 43965, Big Power y He-man), hasta susceptible (Beaufort, Maxifort). Por encima de 28˚C, sólo dos patrones (PG-76 y He-man) inhibieron la reproducción del nematodo. Frente a distintas poblaciones de M. arenaria, M. incognita y M. javanica, el patrón PG-76, fue altamente resistente a todas las poblaciones, Brigeor osciló entre altamente resistente y moderadamente resistente, mientras que Beaufort y Maxifort mostraron menor resistencia o fueron totalmente susceptibles; además ésta varió en función de la población analizada. Se caracterizó molecularmente el locus Mi-1 en los patrones híbridos y cultivares de tomate estudiados. Se emplearon los marcadores moleculares PM3, PMi y Mi23, específicos para la caracterización del locus Mi en patrones híbridos de tomate (S. lycopersicum × S. habrochaites; S. lycopersicum × S. chilense), mediante PCR. También se realizaron análisis bioinformáticos con marcadores específicos (Mint-up/do, C172, C2S4, IMO-F1/R1, y VIGS) para determinar la presencia del gen Mi-1.2 en dichos patrones. Los resultados mostraron que los marcadores PMi y Mi23 amplifican homólogos del gen Mi-1 en S. chilense, S. habrochaites y S. peruvianum y también en S. lycopersicum (marcador Mi23). El marcador PM3 amplificó el gen Mi-1.2 en Beaufort y Maxifort (S. lycopersicum × S. habrochaites) pero no fue efectivo para los híbridos de S. chilense. El marcador molecular PM3, no pudo determinar la expresión de del gen Mi-1.2 en Beaufort y Maxifort por hallarse fuera de la secuencia codificadora (CDS) del gen. Análisis bioinformáticos indicaron que ningún marcador específico diseñado para el gen Mi-1.2, podía este gen de otros homólogos presentes en S. lypcopersicum y S. peruvianum. El nuevo marcador Pau-Do en combinación con el primer C2S4, amplificaron un fragmento de 1.494 pb en la CDS del gen Mi-1.2 en raíces y hojas de Beaufort y Maxifort. La durabilidad de la resistencia del gen Mi-1 después del cultivo reiterado de patrones de tomate se determinó en ensayos de campo durante tres años consecutivos, empleando PG-76 y Brigeor. El patrón PG-76 fue muy resistente después del 1er ciclo de cultivo, pero mostró resistencia intermedia y suscetibilidad al finalizar el 2o y el 3er año de cultivo, respectivamente. El patrón Brigeor y el cultivar de tomate resistente Monika (control) mantuvieron un nivel de resistencia intermedio al final del 3er cultivo, aunque ensayos posteriores confirmaron la aparición de virulencia. Los resultados mostraron que el cultivo reiterado de patrones de tomate resistentes seleccionó rápidamente aislados virulentos de M. javanica. El fenotipo virulento de estas poblaciones se analizó molecularmente con el marcador MVC, diseñado para distinguir las poblaciones virulentas seleccionadas de Meloidogyne de los aislados naturalmente virulentos. Se analizaron dos poblaciones japonesas seleccionadas de M. incognita y M. javanica, tres poblaciones españolas virulentas seleccionadas, una población naturalmente virulenta y una avirulenta (todas M. javanica). Las muestras de ADN se obtuvieron de individuos juveniles o de hembras adultas y se incluyeron muestras de agua sin nematodos (5 µm filtrada) procedentes del drenaje de una maceta con una planta infectada por una población virulenta japonesa. El marcador MVC amplificó ADN en las muestras de agua pero no en las que sólo contenían ADN de nematodos. Las secuencias de ADN mostraron una estrecha correlación con diversas proteínas de especies de betaproteobacterias. Los experimentos revelaron que el marcador de MVC no está relacionado con un gen de virulencia del nematodo (avr) sino con betaproteobacterias. Finalmente, se estudió la existencia de homólogos del gen Mi en las especies de tomate silvestre Solanum chilense, S. habrochaites, S. peruvianum y S. huaylasense. La respuesta de resistencia de la variedad LA-1358 de S. huaylasense varió en función de la especie del nematodo estudiada: fue resistente frente a M. arenaria y susceptible frente a M. javanica. La reproducción de M. incognita fue muy variable y no difirió de la reproducción alcanzada en los dos cultivares empleados como controles. / The response of 10 Mi-1 tomato rootstocks to a Mi-avirulent population of M. javanica was determined in pot tests conducted in a greenhouse in spring when temperatures remained below the Mi-1 functionality resistance threshold (28 ˚C), and in summer when daily temperatures exceeded the Mi-1 expression threshold. Rootstocks were also evaluated in the field exposing them to high population densities of the nematode. Results on infectivity and reproduction below 28 ˚C indicated a wide variability in the resistance response of the rootstocks ranging from highly or intermediate resistance (PG-76, Gladiator, MKT-410; Brigeor, 42851, 43965, Big Power and He-man) to fully susceptible (Beaufort and Maxifort). At high temperature conditions, only PG-76 and He-man inhibited the reproduction of M. javanica. Rootstocks PG-76, Brigeor, Beaufort and Maxifort were challenged to different populations of M. arenaria, M. incognita and M. javanica. Rootstock PG-76 was highly resistant to all the populations tested, whereas the response of Brigeor ranged from highly to moderate resistance; the resistance response of rootstocks Beaufort and Maxifort varied according to the population tested. Molecular characterization of the resistance phenotype was performed for all the tomato hybrid rootstocks and cultivars tested. The markers PM3, PMi, Mi23, for the characterization of the Mi-locus of hybrid tomato rootstocks (S. lycopersicum × S. habrochaites and S. lycopersicum × S. chilense) were used for PCR reactions. In silico analyses were done with specific markers for the Mi-1.2 gene (Mint-up/do, C1/2, C2S4, IMO-F1/R1, and VIGS). Markers PMi and Mi23 were polymorphic for the Mi-1 locus in wild Solanum species (S. chilense, S. habrochaites, and S. peruvianum) and for S. lycopersicum (marker Mi23). Marker PM3 detected the Mi-1.2 gene in S. lycopersicum × S. habrochaites hybrid rootstocks, but not in the S. chilense hybrids. As marker PM3 is located outside the coding sequence of the Mi-1.2 gene, expression of this homolog could not be determined in Beaufort and Maxifort. In silico results indicated that none of the available markers for the Mi-1.2 gene could distinguish this homolog from the other Mi-homologs from S. lypcopersicum and S. peruvianum species. A new marker Pau-Do, in combination with C2S4, was designed to amplify in CDS of the Mi-1.2 gene. Amplification with these primers of cDNA from Beaufort and Maxifort indicated that the Mi-1.2 gene was expressed in both rootstocks, despite their susceptible phenotypic response to some Meloidogyne populations. The durability of the Mi-1 gene after repeated cultivation of resistant tomato rootstocks (PG-76 and Brigeor) was determined through field trials during three consecutive years. Rootstock PG-76 responded as highly resistant after the first cropping cycle, although it became fully susceptible after the second and the third cropping cycles. Rootstock Brigeor and the resistant tomato cultivar Monika (control), retained intermediate resistance levels at the end of the third year. Bioassays confirmed that selection of virulence occurred more rapidly in plots with rootstock PG-76 followed by Brigeor and the resistant tomato cultivar Monika. The virulent phenotype of the selected M. javanica populations in the field experiments was determined with MVC molecular marker, designed to distinguish selected from naturally virulent populations of Meloidogyne spp. The populations analyzed included two Japanese selected virulent populations, and the three virulent populations selected in the field trials, and one naturally virulent population and one avirulent population from Spanish. DNA samples were obtained from individual juveniles (J2) or adult females from all the selected virulent populations. Experiments included water samples free of nematodes (5-µm filtered), obtained from the draining-water of a plant infected by a Japanese selected virulent population. Amplification of DNA only occurred in samples of filtered water, but not in those containing only nematode genetic material. Sequencing and BLAST of the DNA fragments amplified by the MVC molecular marker, established a strong correlation of the amplified bands with proteins from betaproteobacteria species Overall, these results showed that the MVC marker is not related to a nematode virulence gene (avr) but to betaproteobacteria. New root-knot nematode resistant Mi-homologs were searched in accessions of the wild Solanum species. The S. huaylasense accession LA-1358 reduced reproduction of a population of M. arenaria to similar levels than the resistant tomato cultivar Anairis. Nevertheless, the resistance response of S. huaylasense accession LA-1358 was also nematode-species specific.

Submitted by Marco Antônio de Ramos Chagas (mchagas@ufv.br) on 2017-04-27T18:33:44Z No. of bitstreams: 1 texto completo.pdf: 878289 bytes, checksum: 70c4ac466fdd682cb943dce260aec8df (MD5) / Made available in DSpace on 2017-04-27T18:33:44Z (GMT). No. of bitstreams: 1 texto completo.pdf: 878289 bytes, checksum: 70c4ac466fdd682cb943dce260aec8df (MD5) Previous issue date: 2004-08-27 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Experimentos foram conduzidos em laboratório e casa de vegetação objetivando o aprimoramento do método clássico de multiplicação de Pasteuria penetrans ‘in vivo’, proposto em 1980 por Stirling e Wachtel. No primeiro experimento comparou-se a produção de endósporos da P. penetrans em raízes de tomateiro de crescimento indeterminado cv. Santa Clara e determinado cv. TRural 1. Maiores pesos de matéria fresca e seca e número de endósporos foram observados em tomateiro cv. Santa Clara. O segundo experimento foi realizado para determinar a concentração ideal de endósporos de P. penetrans na suspensão e o tempo de agitação necessário para adesão adequada de endósporos aos nematóides para multiplicação da bactéria. Para que se obtenham seis endósporos, em média, por juvenil de segundo estádio (J2) de Meloidogyne javanica, verificou-se serem necessárias suspensões contendo 3,3 x 10 5 endósporos/mL, agitadas por 10 a 20 minutos, ou 3,3 x 10 4 endósporos/mL por 50 minutos. Em outro ensaio, comparou-se a multiplicação de P. penetrans em população pura de M. incognita ou em população composta de M. incognita e M. javanica oriunda de um campo de cultivo de tomate. A produção de endósporos de P. penetrans em tomateiro inoculado com M. incognita foi aproximadamente três vezes superior àquela em plantas inoculadas com população mista. Realizou-se também um teste de adesão de P. penetrans às duas populações do nematóide. Foi observado maior número de endósporos aderidos aos J2 de M. incognita. A produção de endósporos da P. penetrans em plantas de tomateiro cv. Santa Clara com 15, 30, 45 ou 60 dias de idade e inoculadas com 5.000, 15.000 ou 25.000 J2 foi avaliada. As plantas com 30 e 45 dias de idade inoculadas com 25.000 J2 permitiram a multiplicação de P. penetrans cerca de 19 vezes maior àquela obtida em plantas inoculadas com 5.000 J2. Com o objetivo de determinar se maiores níveis de matéria orgânica adicionada ao substrato provocavam alterações fisiológicas nos nematóides ou nas plantas de tomate, estudou-se a influência de diferentes proporções de solo, areia e esterco de curral (1:1:0, 2:2:1, 1:1:1 ou 1:1:2 (V:V:V), respectivamente) e três níveis de inóculo de espécies de Meloidogyne (3.000, 6.000 e 9.000 J2) sobre a concentração de fenóis em raízes de tomateiro, no teor de lipídios de espécies de Meloidogyne, e em possíveis alterações em células gigantes induzidas por esses nematóides. Não se observou efeito dos tratamentos no teor de lipídios dos nematóides. A concentração de fenóis nas raízes aumentou à medida que se acrescentou mais esterco de curral ao substrato ou quando as plantas foram inoculadas com mais nematóides (9.000 J2). As células gigantes em raízes de plantas cultivadas nos substratos 1:1:0 e 2:2:1 (solo:areia:esterco) foram mais numerosas, maiores e com maior número de núcleos. Por outro lado, as células gigantes de plantas cultivadas no substrato 1:1:1 e 1:1:2, além de menos numerosas, apresentaram alterações no tamanho e formato, demonstrando o efeito deletério das maiores doses de esterco sobre esses sítios de alimentação. O último ensaio foi conduzido para avaliar o efeito de crescentes quantidades de esterco de curral nos substratos e níveis de inóculo de espécies de Meloidogyne na reprodução de P. penetrans. Maior percentual de fêmeas infectadas por P. penetrans foi observado quando se utilizou o substrato 1:1:0 em relação aos substratos 1:1:1 e 1:1:2 ou quando as plantas foram inoculadas com 3.000 J2. O experimento foi repetido uma vez e na primeira condução do experimento, plantas cultivadas no substrato 1:1:0 ou inoculadas com 9.000 J2 apresentaram maior número de endósporos; entretanto, na segunda condução do experimento as plantas inoculadas com 9.000 J2 e cultivadas no substrato 2:2:1 foram as que permitiram maior reprodução de P. penetrans. / Greenhouse and laboratory experiments were conducted to improve the classical method of multiplying P. penetrans ‘in vivo’, proposed by Stirling & Wachtel in 1980. In the first experiment, the mass production of P. penetrans in tomatoes of indeterminated and determinated growth, cv. Santa Clara and Trural I, respectively, was compared. Higher fresh and dry root weight and endospore number were observed in ‘Santa Clara’ tomato. The second experiment was conducted to determine the best endospore concentration of P. penetrans in the aqueous suspension and the time of shaking necessary to obtain adequate attachment of endospores on the nematodes, as the first step for P. penetrans multiplication. To obtain an average of six endospores per second stage juvenile (J2) of M. javanica, it is necessary to shake suspension of 3,3 x 10 5 endospores/mL per 10 to 20 minutes or to shake 3,3 x 10 4 endospores/mL for 50 minutes. In another experiment, the reproduction of P. penetrans in pure population of M. incognita and in a mixed population of M. incognita and M. javanica, originated from the field, was studied. The endospore production of P. penetrans in tomato plants inoculated with M. incognita was approximately three times higher than in plants inoculated with the field population. An attachment test of P. penetrans on the two populations was performed and higher number of endospores attached to J2 of M. incognita was observed. The multiplication of P. penetrans in 15, 30, 45 or 60 day-old ‘Santa Clara’ tomato plants inoculated with 5,000, 15,000 or 25,000 J2, was also evaluated. The 30 and 45 days old plants inoculated with 25,000 J2 provided P. penetrans multiplication up to nineteen times more than plants inoculated with 5,000 J2 in the first experimental run. To determine if high cow manure levels added to substrate promote physiological changes on the nematodes or on the tomato plants, the influence of cow manure amendment to mixtures of soil and sand giving rates of 1:1:0; 2:2:1; 1:1:1 and 1:1:2 (V:V:V) of soil, sand and manure, respectively, and three inoculum levels of Meloidogyne species, i.e., 3,000; 6,000 and 9,000 J2 on the phenolic content in the tomato roots, changes in nematode lipid content and possible alterations in the giant cells induced by the nematodes, were studied. No conclusion could be drawn about the effect of manure on the nematode lipid content. The phenolic content in the roots increased as more cow manure was added to the substrate or when the plants were inoculated with more nematodes (9,000 J2). The giant cells in the roots of plants cultivated in the substrates 1:1:0 and 2:2:1 were more numerous, bigger and with more nuclei. On the other hand, the giant cells of plants cultivated on 1:1:1 and 1:1:2 substrates were less numerous, showed changes on their format and were smaller, demonstrating the deleterious effect of organic amendments to these feeding sites. A subsequent experiment was carried out to evaluate the effect of the interaction of increasing rates of cow manure in the substrates and of nematode levels on the reproduction of Pasteuria penetrans. Higher perceptual of infected females by P. penetrans was observed when the plants grew in the substrate 1:1:0 than in the substrates 1:1:1 and 1:1:2, or when plants were inoculated with 3,000 J2. The experiment was repeated once and in the first run, plants cultivated on substrate 1:1:0 or inoculated with 9,000 J2 had higher endospore number. However, in the second run, plants inoculated with 9,000 J2 and cultivated on substrate 2:2:1 yielded more endospores per root system. / Tese importada do Alexandria

Orientador: Rumy Goto / Banca: Roberto Lyra Villas Bôas / Banca: Dirceu Maximino Fernandes / Banca: Sebastião Wilson Tivelli / Banca: Arlete Marchi Tavares de Melo / Resumo: Avaliou-se a produtividade, o acúmulo e a exportação de nutrientes por plantas de pimentão (Capsicum annuum L.) enxertadas e não enxertadas, cultivadas sob ambiente protegido. O experimento foi conduzido de agosto de 2003 a maio de 2004 na Escola Técnica Estadual Augusto Tortolero Araújo pertencente ao Centro Estadual de Educação Tecnológica Paula Souza, em Paraguaçu Paulista, SP. Os porta-enxertos utilizados, AF 2638 e AF 2640, possuem resistência à Phytophthora capsici Leonian e Meloidogyne incognita raça 2. Os tratamentos constaram dos híbridos 'Rúbia R' e 'Margarita' sem enxertar, enxertados sobre os dois porta-enxertos e enxertados neles mesmos. O delineamento experimental foi em blocos ao acaso com oito tratamentos, quatro repetições e 15 plantas por parcela. As plantas foram avaliadas quanto a altura da maior haste, altura da primeira bifurcação, precocidade de florescimento, comprimento e número médio de internódios, produção e características dos frutos produzidos em 12 colheitas, massa de matéria verde e seca de folhas, caules e frutos. As análises químicas foram realizadas em uma planta por parcela aos 35, 83, 135, 178 e 213 dias após o transplante, para determinar a marcha de absorção e exportação de nutrientes. Verificou-se que os híbridos enxertados e não enxertados apresentaram produtividades médias de 132 e 153 t ha-1 para as combinações enxertadas de 'Rúbia R' e 'Rúbia R' pé-franco respectivamente e de 144 e 132 t ha-1 para as combinações enxertadas de 'Margarita' e 'Margarita' pé-franco respectivamente. O acúmulo de nutrientes não foi significativamente diferente entre plantas enxertadas e pés-francos, e a ordem decrescente dos nutrientes acumulados foi: K>N>Ca>Mg>P>S. A partir do que foi observado, concluiu-se que, nessas condições, a enxertia em plantas de pimentão não alterou seu desempenho agronômico, nem teve influência sobre a marcha de absorção de nutrientes. / Abstract: It was evaluated the yield, accumulation and exportation of nutrients by sweet pepper plants grafted and non grafted, under protected cultivation. The research was carried out from August 2003 to May 2004, at the Technical School Augusto Tortolero Araújo, part of Paula Souza State Center of Technological Education, in Paraguaçu Paulista, SP, in Brazil. The rootstocks used - AF 2638 and AF 2640, are resistant to Phytophthora capsici Leonian and Meloidogyne incognita race 2. The treatments were constituted of non grafted hybrids 'Rúbia R' and 'Margarita'; grafted on two evaluated rootstocks and grafted on themselves. The experimental design was of completely randomized blocks with eight treatments, four replications and fifteen plants per plot. Five plants were sent for chemical analysis. Evaluations of the total plants height, first fork height, early blossom, length and average number of internodes, total yield and fruits characteristics of 12 harvests, fresh and dry matter of leaves, stems and fruits, were carried out. The samples for the chemical analysis were taken at the 35th, 83th, 135th, 173th and 213th days after transplantation, with the objective of determining the accumulation and exportation of the nutrients. The results proved that the grafted and non grafted plants had average yield, with the average of 132 and 153 t ha-1 for the grafted combinations of 'Rúbia R' and non grafted plants of 'Rúbia R' respectively and 144 and 132 t ha-1 for the grafted combinations of 'Margarita' and non grafted plants of 'Margarita' respectively. The accumulation of the nutrients was equivalent for grafted combinations and non grafted plants, and nutrients in decreasing order of accumulation were: K>N>Ca>Mg>P>S. It was evidenced that grafting sweet pepper plants neither its agronomic performance, nor interfered on the uptake of nutrients' absorption. / Doutor

A infestação de áreas com Meloidogyne exigua é um dos principais fatores limitantes ao desenvolvimento da heveicultura brasileira. Estudos anteriores demonstraram que o nematoide afeta o crescimento da seringueira, reduzindo o desenvolvimento de árvores que estão em fase produtiva podendo comprometer até mesmo a sua sobrevivência. Nesse contexto, o objetivo do presente estudo foi avaliar a distribuição espacial e nível populacional de M. exigua em um seringal e seu controle com plantas antagonistas. Para tanto, foram montados dois experimentos. O primeiro avaliou a distribuição espacial e o nível populacional do nematoide de galha em um plantio comercial de seringueira no Triângulo Mineiro, Minas Gerais. Constatou-se que o nível populacional de M. exigua, na área estudada, concentrou-se em focos elípticos – reboleiras – e sua distribuição espacial era do tipo agregada. O segundo experimento avaliou o efeito das plantas antagonistas Arachis repens, Brassica juncea, Brassica napus, Crotalaria spectabilis, Tagetes sp. consorciadas com mudas de seringueira no controle de Meloidogyne exigua. As plantas Arachis repens, Brassica juncea, Brassica napus e Tagetes sp. demonstraram efeito antagônico sobre a população do nematoide. Os resultados obtidos evidenciam a importância do manejo para expansão da heveicultura brasileira. / The infestation of nematodes of the genus Meloidogyne is one of the main limiting factors for the expansion of Brazilian rubber tree plantations. Previous studies have shown that this root-knot nematode affects growth of the rubber tree, thus reducing the development of trees in the production phase and even jeopardizes its survival. In this context, the objective of this study was to evaluate the spatial distribution of Meloidogyne exigua in a rubber tree plantation and its control with antagonistic plants. In order to perform this, two experiments were done. The first one evaluated the population density of the root-knot nematode in a commercial rubber tree plantation in Triângulo Mineiro, Minas Gerais. The population density of M. exigua, in the studied area, was concentrated in elliptic foci with a clustered spatial distribution. The second experiment evaluated the effect of the antagonistic plants Arachis repens, Brassica juncea, Brassica napus, Crotalaria spectabilis, and Tagetes sp. on the management of M. exigua in rubber tree seedlings. Both Brassica juncea and Arachis repens showed antagonistic effect on nematode population. The results obtained highlight the importance of proper nematode management for the expansion of Brazilian rubber tree plantations. / Dissertação (Mestrado)

Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico / Este trabalho descreve o estudo dos componentes volÃteis e nÃo volÃteis das raÃzes de Petiveria alliaceae, incluindo as atividades nematicida e inseticida do Ãleo essencial. Para o estudo quÃmico, fitonematicida e inseticida utilizou-se as raÃzes da planta, das quais foram obtidos o Ãleo essencial e os constituintes nÃo-volÃteis. Do Ãleo essencial das raÃzes foram identificados os seguintes componentes: benzaldeido (61,5%) (constituinte majoritÃrio) dissulfeto de dibenzila (18,1%), transestilbeno (14,1%) e cinamaldeido (6,3%), sendo que esses dois Ãltimos compostos tambÃm foram isolados atravÃs de cromatografia em camada delgada preparativa e identificados por RMN 1H e 13C. O tratamento cromatogrÃfico dos extratos etanÃlico, acetato de etila e hexÃnico permitiu o isolamento de uma mistura de duas mercaptanas, dissulfeto de dibenzila e o trissulfeto de dibenzila, dissulfeto de dibenzila, uma alantoina e a sacarose, que pela primeira vez foram isoladas das raÃzes de Petiveria alliaceae. As mercaptanas isoladas sÃo conhecidas na literatura por suas atividades fungicidas e nematicida. O Ãleo essencial extraÃdo das raÃzes de P. alliaceae e seus constituintes foram submetidos aos ensaios de atividades nematicida contra larvas de Meloidogyne incÃgnita (nematÃide de galhas) e inseticida contra a Mosca branca (Bemisia tabaci) inseto do feijÃo (Callosobruchus maculatus). Os Ãleos essenciais obtidos de P. alliaceae coletadas nas duas localidades diferentes apresentaram significantes atividades inseticida e nematicida. Os constituintes isolados tiveram suas estruturas elucidadas atravÃs de mÃtodos espectromÃtricos de IV, EM, RMN 1H e 13C uni e bidimensionais (COSY, HMQC e HMBC). / This work describes the study of the volatile and the non-volatile components from the roots of Petiveria alliaceae, including the nematicidal and insecticidal activities of the essential oil. The following components were identified in the essential oil: benzaldehyde as the major constituent (61, 5 %), cinnamaldehyde (6, 3%), dibenzyl disulphide (18, 1%), transstilbene (14, 1%). The two last compounds were also isolated through a chromatography in a preparative thin layer identified by RMN 1H and 13C. The isolation of a mixture of two mercaptans, benzyl disulphide and dibenzyl trisulphide, saccharose and allantoin, which were isolated for the first time from the Petiveria alliaceae, was permitted by the chromatographic treatment of the ethyl acetate, hexane, and ethanolic extracts. The isolated mercaptans are known in literature for their fungicide and insecticide activities. The constituents of the essential oil, extracted from the roots of Petiveria alliaceae, were submitted to the nematicidal activities against Meloidogyne incognita larva, insecticide against white fly (Bemisa tabaci) and insect of the beans (Callosobruchus maculatos). Significant insecticidal and nematicidal activities were present in the essential oil from the P. alliaceae, collected in two different localities. The isolated constituents had their structure elucidated through spectrometric methods of IV, EM, RMN 1H and 13C uni and bi-dimensional (COSY, HMQC and HMBC)

Made available in DSpace on 2014-08-20T14:22:08Z (GMT). No. of bitstreams: 1 Tese_Luciane_Arantes_de_Paula.pdf: 858789 bytes, checksum: 8b70288e22f4a33dd49c0ffd4f1e0624 (MD5) Previous issue date: 2009-07-23 / The Rio Grande do Sul state (RS) represents great importance in the stone fruit, with approximately 65% of the area cultivated with peach country. This should highlight the contribution of the breeding of new cultivars crown, which extend the period allowed for collection and quality of fruit. Still, the average productivity in the RS is still considered low, mainly due to lack of knowledge about factors related to incidence of pests, diseases and lack of root stock suitable for cultivation, because unlike other countries, the improvement in Brazil genetic of the rootstocks for stone fruit of importance has taken only a few years ago. This thesis is divided into three chapters, with chapter 1 was to evaluate the reaction of five peach rootstocks, from front to inoculation with Meloidogyne incognita, in a home-de-vegetation. And we can conclude that 'Selection UFPel-0402', 'Okinawa', 'Flordaguard', Nagano Wild‟ and 'Select NR-0080407' are immune to Meloidogyne incognita, and may be used in genetic improvement programs for the rootstocks of peach and as alternative use for the deployment of orchards in areas with occurrence of the pest, and the strength of the 'Nagano Wild' needs further studies to identify more clearly this characteristic. Chapter 2 objective evaluated the genetic variability and differentiation of 14 rootstocks, peach, setting a standard for molecular characterization of each genotype, based on loci of SSR, SCAR and STS, for future work on genetic improvement and it is concluded that markers of microsatellites can be relatively easily a pattern of molecular genotypes of the rootstocks of peach and solve problem of homonymy, the example of the evaluated genotypes of Okinawa, and shows which are more contrasting genotypes for use in breeding. Chapter 3 objective to estimate frequencies of recombination among molecular markers, and the color of leaf, from the analysis of a F2 segregating population ('Capdeboscq' x 'Flordaguard'), and check if the connection is similar to that obtained in other mapping populations. It can be concluded that based on molecular maps for Prunus spp. available in the literature and from results obtained in this work, it was concluded that the markers UDP96-013 and BPPCT-034 are linked in different mapping populations, and potential candidates for use in the selection of new resistant genotypes to Meloidogyne spp. . / O Rio Grande do Sul (RS) é o principal produtor de frutas de caroço do Brasil, com aproximadamente 65% da área cultivada com pêssego do país. Esse destaque se deve a contribuição dos programas de melhoramento genético de novas cultivares copa, que possibilitou ampliar o período de colheita e a qualidade das frutas. Mesmo assim, a produtividade média no RS ainda é considerada baixa, principalmente devido à falta de conhecimento sobre fatores relacionados à incidência de pragas, doenças e a falta de porta-enxertos adequados para a cultura, pois ao contrário de outros países, no Brasil o melhoramento genético de porta-enxertos para frutíferas de caroço tem assumido importância apenas há poucos anos. Esta tese está dividida em três capítulos, sendo que o capítulo 1 teve como objetivo avaliar a reação de cinco porta-enxertos de pessegueiro à Meloidogyne incognita, em condições de casa-de-vegetação. Pode-se concluir que Seleção UFPel-0402‟, Okinawa‟, Flordaguard‟, Nagano Wild‟ e Seleção NR-0080407‟ são imunes a Meloidogyne incognita, podendo ser utilizados em programas de melhoramento genético de porta-enxertos de pessegueiro e também como alternativa de uso para implantação de pomares em áreas com ocorrência da praga. A resistência do Nagano Wild‟ necessita de estudos complementares para identificar, de forma mais clara, a amplitude dessa característica. No capítulo 2 objetivou-se avaliar a variabilidade genética e diferenciar 14 porta-enxertos de pessegueiro, estabelecendo-se um padrão molecular de caracterização para cada genótipo, baseado em locos de SSR, SCAR e STS, para futuros trabalhos de melhoramento genético. Neste estudo concluindo-se que marcadores de microssatélites permitem estabelecer com relativa facilidade um padrão molecular de genótipos de porta-enxertos de pessegueiro e resolver problema de homonímia, a exemplo dos genótipos de Okinawa avaliados, bem como seu uso permite verificar quais genótipos são mais contrastantes para uso em melhoramento genético. O capítulo 3 teve como objetivo estimar freqüências de recombinação, entre marcadores moleculares e o caractere cor de folha, a partir da análise de uma população F2 segregante ( Capdeboscq‟ x Flordaguard‟), e também verificar se a ligação ocorre de forma similar ao obtido em outras populações de mapeamento. Foram avaliados nove locos de microssatélites, sendo possível verificar, com base nos dados do presente trabalho e em mapas moleculares para Prunus spp. disponíveis na literatura, que os marcadores UDP96-013 e BPPCT-034 estão ligados em diferentes populações de mapeamento, sendo potenciais candidatos para uso na seleção de novos genótipos resistentes à M. incognita.