Terra Incognita: A symbolic mythical journey

This practice-led project is implemented in the context of rites of passage based on significant events in formative transitions of Self. It employs an intuitive methodology to examine and explore the 'Child archetype', mythos, symbolic imagination and self-narrative, through the manifestation of a visual symbolic language. The contexts, methods and processes enable empowerment, heightened awareness of personal and collective relationships, meaningful discovery and development of innovative ideas and forms. The implications for this project highlight the importance of intuition in creativity and innovation. Creative practice is a vehicle for personal and collective interconnectedness. I have discovered self-empowerment, meaningful learning and innovative forms of personal and collective communication as a way of enabling transition of a significant life event.

Resistance of Brassicaceae plants to root-knot nematode (Meloidogyne spp.) in northern Australia

Brassicaceae plants have the potential as part of an integrated approach to replace fumigant nematicides, providing the biofumigation response following their incorporation is not offset by reproduction of plant-parasitic nematodes on their roots. Forty-three Brassicaceae cultivars were screened in a pot trial for their ability to reduce reproduction of three root-knot nematode isolates from north Queensland, Australia: M. arenaria (NQ1), M. javanica (NQ2) and M. arenaria race 2 (NQ5/7). No cultivar was found to consistently reduce nematode reproduction relative to forage sorghum, the current industry standard, although a commercial fodder radish (Raphanus sativus) and a white mustard (Sinapis alba) line were consistently as resistant to the formation of galls as forage sorghum. A second pot trial screened five commercially available Brassicaceae cultivars, selected for their biofumigation potential, for resistance to two nematode species, M. javanica (NQ2) and M. arenaria (NQ5/7). The fodder radish cv. Weedcheck, was found to be as resistant as forage sorghum to nematode reproduction. A multivariate cluster analysis using the resistance measurements, gall index, nematode number per g of root and multiplication for two nematode species (NQ2 and NQ5/7) confirmed the similarity in resistance between the radish cultivar and forage sorghum. A field trial confirmed the resistance of the fodder radish cv. Weedcheck, with a similar reduction in the number of Meloidogyne spp. juveniles recovered from the roots 8 weeks after planting. The use of fodder radish cultivars as biofumigation crops to manage root-knot nematodes in tropical vegetable production systems deserves further investigation.

Beyond chemical dependency for managing plant-parasitic nematodes: Examples from the banana, pineapple and vegetable industries of tropical and subtropical Australia

Plant-parasitic nematodes are important pests of horticultural crops grown in tropical and subtropical regions of Australia. Burrowing nematode (Radopholus similis) is a major impediment to banana production and root-knot nematodes (predominantly Meloidogyne javanica and M. incognita) cause problems on pineapple and a range of annual vegetables, including tomato, capsicum, zucchini, watermelon, rockmelon, potato and sweet potato. In the early 1990s, nematode control in these industries was largely achieved with chemicals, with methyl bromide widely used on some subtropical vegetable crops, ethylene dibromide applied routinely to pineapples and non-volatile nematicides such as fenamiphos applied up to four times a year in banana plantations. This paper discusses the research and extension work done over the last 15 years to introduce an integrated pest management approach to nematode control in tropical and subtropical horticulture. It then discusses various components of current integrated pest management programs, including crop rotation, nematode monitoring, clean planting material, organic amendments, farming systems to enhance biological suppression of nematodes and judicious use of nematicides. Finally, options for improving current management practices are considered.

Linalyl Acetate Is Metabolized by Pseudomonas incognita with the Acetoxy Group Intact

Metabolism of linalyl acetate by Pseudomonas incognita isolated by enrichment culture on the acyclic monoterpene alcohol linalool was studied. Biodegradation of linalyl acetate by this strain resulted in the formation of linalool, linalool- 8-carboxylic acid, oleuropeic acid, and A5-4-acetoxy-4-methyl hexenoic acid. Cells adapted to linalyl acetate metabolized linalyl acetate-8-aldehyde to linalool- 8-carboxylic acid, linalyl acetate-8-carboxylic acid, A5-4-acetoxy-4-methyl hexenoic acid, and geraniol-8-carboxylic acid. Resting cell suspensions previously grown with linalyl acetate oxidized linalyl acetate-8-aldehyde to linalyl acetate-8- carboxylic acid, A5-4-acetoxy-4-methyl hexenoic acid, and pyruvic acid. The crude cell-free extract (10,000 g of supernatant), obtained from the sonicate of linalyl acetate-grown cells, was shown to contain enzyme systems responsible for the formation of linalyl acetate-8-carboxylic acid and linalool-8-carboxylic acid from linalyl acetate. The same supernatant contained NAD-linked alcohol and aldehyde dehydrogenases involved in the formation of linalyl acetate-8-aldehyde and linalyl acetate-8-carboxylic acid, respectively. On the basis of various metabolites isolated from the culture medium, resting cell experiments, growth and manometric studies carried out with the isolated metabolites as well as related synthetic analogs, and the preliminary enzymatic studies performed with the cellfree extract, a probable pathway for the microbial degradation of linalyl acetate with the acetoxy group intact is suggested.

Metabolism of alpha-terpineol by Pseudomonas incognita

Details of the metabolism of alpha-terpineol by Pseudomonas incognita are presented. Degradation of alpha-terpineol by this organism resulted in the formation of a number of acidic and neutral metabolites. Among the acidic metabolites, beta-isopropyl pimelic acid, 1-hydroxy-4-isopropenyl-cyclohexane-1-carboxylic acid, 8-hydroxycumic acid, oleuropeic acid, cumic acid, and p-isopropenyl benzoic acid have been identified. Neutral metabolites identified were limonene, p-cymene-8-ol, 2-hydroxycineole, and uroterpenol. Cell-free extracts prepared from alpha-terpineol adapted cells were shown to convert alpha-terpineol, p-cymene-8-ol, and limonene to oleuropeic acid, 8-hydroxycumic acid, and perillic acid, respectively, in the presence of NADH. The same cell-free extract contained NAD+ -specific dehydrogenase(s) which converted oleuropyl alcohol, p-cymene-7,8-diol, and perillyl alcohol to their corresponding 7-carboxy acids. On the basis of various metabolites isolated from the culture medium, together with the supporting evidence obtained from enzymatic and growth studies, it appears that P. incognita degrades alpha-terpineol by at least three different routes. While one of the pathways seems to operate via oleuropeic acid, a second may be initiated through the aromatization of alpha-terpineol. The third pathway may involve the formation of limonene from alpha-terpineol and its further metabolism.

Metabolism of structurally modified acyclic monoterpenes by Pseudomonas incognita

The ability of Pseudomonas incognita to metabolize some structurally modified acyclic monoterpenes was tested. The 6,7 double bond was found essential for these compounds to serve as a substrate for this organism, whereas the same was not true with the 1,2 double bond. Metabolism of dihydrolinalyl acetate by this strain yielded dihydrolinalool, dihydrolinalool-8-carboxylic acid, dihydrolinalyl acetate-8-carboxylic acid, and 4-acetoxy-4-methyl hexanoic acid. A cell-free extract prepared from dihydrolinalyl acetate grown cells transformed dihydrolinalyl acetate into dihydrolinalool and dihydrolinalool-8-carboxylic acid. Based on the identification of various metabolites isolated from the culture medium, and on growth and manometric studies carried out with the isolated metabolites as well as with related synthetic analogs, probable pathways for the biodegradation of dihydrolinalyl acetate are presented.

Efecto de Neem (Azadirachta indica J.) y Curater sobre meloidogyne y Rotylenchulus spp en tomate (Lycopersicum esculentum M.) a nivel de invernadero

Este experimento fue conducido en la Universidad Nacional Agraria (U.N.A.) a nivel de Invernadero, durante los meses de julio a octubre de 1991, con el objetivo de conocer a través de la evaluación el efecto de neem (Azadirachta indica J.) como nematicida en relación a la aplicación de curater 10G. Se utilizó un Diseño de Parcelas Divididas con dos factores: factor tratamiento con 4 niveles y el factor tiempo con 6 diferentes fechas, esto se realizó para la variable nematodos de suelo. Para el variable número de nematodos de raíz y número de nódulos se utilizó un Diseño de Bloques Completamente Aleatorizado (B. C.A.) Con 4 niveles del factor tratamiento y 6 diferentes fechas. Se realizaron muestreos semanales de suelo y raiz para evaluar las poblaciones de Rotylenchulus y Meloidogyne spp por un periodo de seis semanas. En los resultados neem mostró un índice de efectividad de un 60 a 75% y curater 10G mostró un índice de un 30 a 40%.

Patogenicidad de Fusarium oxysporum fs. y su interacción con meloidogyne sp. en el complejo de la marchitez lenta de cafe

El presente estudio se llevó a cabo de Julio de 1994 a Julio de 1996. Con los objetivos de: (1) Evaluar la Patogenicidad Fusarium oxysporum, sobre el cultivo del café empleando dos métodos de inoculación, un método con navaja, y un método de poda de raíces con inmersión (2) Evaluación de la Interacción Meloidogyne -Fusarium en plantas de café injertadas y no injertadas y, (3) Evaluar el efecto de la interacción Meloidogyne -Fusarium sobre el desarrollo de la marchitez lenta en el comportamiento de la variedad Catrenic. El estudio se dividio en dos fases una fase de campo y una fase de laboratorio. La fase de campo concistió de tres ensayos: Ensayo 1 Evaluación de la patogenicidad de Fusarium oxysporum fs. Cuyos resultados indicaron diferencias significativas en el método de Inmersión concluyendo, que es el método de inoculación más efectivo, para comprobar que Fusarium puede penetrar con mayor rápidez dentro de la planta y causar infección en estas. Ensayo 2 Interacción Meloidogyne sp. - Fusarium oxysporum en plantas de café con injerto y sin injertó,como resultado de este ensayo, las plantas más afectadas en su altura, diámetro del tallo, peso fresco de raíz, e indica de agallas fueron las plantas sin injer.to presentando una menor tolerancia al ataque de nematodos y por ende reflejaron una mayor evidencias de síntomas de la enfermedad marchitez lenta. Ensayo 3 Evaluación de la interacción Meloidogyne sp. - Fusarium oxysporum en la marchitez lenta con la variedad Catrenic. Los resultados de este ensayo demostrarán que Meloidogyne y Fusarium actúan sinergisticamente causando un cuadro claro de deterioro de las plantas de café de la variedad Catrenic.

Evaluación de Paecilomyces lilacinus como controlador biológico de Meloidogyne exigua en el cultivo del café en la IV región

Con el objetivo de evaluar la efectividad del hongo paecilomyces lilacinus como controlador biológico de embriones de meloidogyne exigua y compararlo con el control químico de carbufuran en vivero de café (coffea arábica l.), se realizó entre los meses de abril a diciembre de 1986 en la estación experimental jardín botánico de masatepe, departamento de Carazo, la evaluación de seis tratamiento. El experimento se efectuó en una parcela de 37m2, con cinco repeticiones de un diseño experimental en bloques completo al azar. Se evaluaron las cuatro plantas centrales de cada parcela, en total 120 plantas. El manejo del experimento se basó en la técnica de reaislamiento, reproducción y aplicación de paecilomyces lilacinus del Dr. Parviz jalata (18) y siguiendo las técnica del cultivo del café utilizada en la lV región. Los tratamiento comparados; 3 dosis de arroz cubiertos de colonias de paecilomyces lilacinus; 15 gramos, 10gramos y 5 gramos, respectivamente, furadan 5G a la dosis de 5 gramos y todos los anteriores, incluyendo el testigo relativo con una aplicación de 1000 larvas de meloidogyne exigua por cada planta y un testigo absoluto; todos en bolsas de polietileno con capacidad de 2 kilos de suelo. Los tratamientos que presentaron mejor control de la población nematologica son paecilomyces lilacinus a razón de 5g. y furadan 5G a razón de 5g. y el testigo absoluto. En condiciones de laboratorio se comprobó la efectividad del hongo, donde la agresividad para destruir embriones de meloidogyne exigua fue directamente proporcional a la mayor concentración de esporas del hongo (1 *10 esporas/ml) y al tiempo de exposición a este

Controle de Meloidogyne javanica em tomate-salada e feijao-de-vagem com o cultivo previo de Crotalaria spectabilis.

O feijão-de-vagem é uma hortaliça severamente atacada por Meloidogyne javanica quando cultivada após o tomate-salada. Para avaliar a viabilidade de cultivo do feijão-de-vagem após o tomate-salada, cultivou-se a Crotalaria spectabilis, em faixas, por período de quatro meses, previamente ao cultivo do tomateiro. Faixas cultivadas com quiabeiro, antes do cultivo com tomate-salada, foram mantidas para comparação. Nas faixas cultivadas anteriormente com C. spectabilis, com os índices de multiplicação (IM) variando de 11 a 76 por parcela e os números de ovos do nematóide de 1.500 a 6.000 por planta, as produtividades foram de 2 a 26% maiores em cultivares de tomateiro e de 6 a 31,5% maiores em cultivares de feijão-de-vagem, em comparação com as produtividades obtidas nas faixas de quiabeiro, onde foram obtidos IM de 17 a 165 e números de ovos do nematóide que variaram de 7.200 a 19.000 por planta em cultivares de tomateiro e de feijão-de-vagem. O cultivo prévio da C. spectabilis por quatro meses é uma tecnologia viável para o controle de M. javanica, viabilizando a seqüência de cultivos com tomate-salada e feijão-de-vagem.

Metodologia para seleção de hortaliças com resistência a nematóides: cenoura/Meloidogyne spp.

Etiologia; Sintomatologia; Variabilidade de espécies dos nematóides; Produção de inóculo; Metodologia de avaliação da resistência; Fator de reprodução dos nematóides (FR); Percentagem de infecção de raízes comerciais; Avaliação da resistência das progênies na Embrapa Hortaliças.

Metodologia para seleção de hortaliças com resistência à nematóides: alface/Meloidogyne spp.

2005

Avaliação de acessos do banco de germoplasma de mandioquinha-salsa da Embrapa Hortaliças para resistência a Meloidogyne spp. no campo.

2007