No description available.

Gossypium hirsutum, upland cotton, is one of the major crops grown in the United States and the world. Upland cotton is cultivated in areas that are ideal breeding grounds for the difficult to manage, southern root-knot nematode (RKN), Meloidogyne incognita. Host plant resistance is the most effective way to control RKN populations. However, resistance used in most breeding programs stems from a few related sources. Novel sources of resistance have been identified but have yet to be introduced into elite breeding lines or genetically studied. The objectives of this study are two-fold. The first is to develop elite germplasm by introgressing RKN resistance from primitive accessions into modern cotton genotypes via backcrossing. The second is to use simple sequence repeats (SSRs) to identify loci associated with RKN resistance in the primitive accessions. The genotypes used will be: 1) inoculated with M. incognita, 2) phenotypically analyzed by measuring the nematode reproduction as eggs per gram of fresh root and host response using a root gall index, 3) genetically evaluated by using SSR markers to detect polymorphisms between the RKN resistant TX accessions and DP90 (susceptible genotype), and 4) analyzed using linkage and mapping software. Elite germplasm that contains: 1) high yield potential and a high level of RKN- resistance or 2) high fiber quality and RKN-resistance was developed by performing two backcrosses based on phenotypic analyses. A third screen is currently underway to ensure the introgression of the RKN resistance genes. Agronomic tests will need to be done before the germplasm is released. Genetic analyses using SSR-based primer sets of the TX accessions did not yield expected results. Of the 508 primers sets tested, only 31 were polymorphic between the TX accessions and DP90. A bulked segregant analysis approach was used to test the 31 primer sets on the resistant and susceptible bulks of the F2 population but no polymorphisms were seen. However, analyses found that the TX accessions were more genetically similar to Mexico Wild Jack Jones than to Clevewilt 6-3-5. More work needs to be done to understand the mechanism of RKN resistance in the TX accessions.

Thesis (M.Sc.(Agric.))--University of Western Australia, 2006.

One of the most economically important pathogens of US soybeans is the Southern Root Knot Nematode [(Meloidogyne incognita) (Kofoid and White) Chitwood] (Mi). Evaluation and identification of resistance is highly important to the plant breeding program at SIUC. The main objective of this study was to screen within the greenhouse two F5:7 recombinant inbred line (RIL) (n=96) from crosses between LS90-1920 or LS97-1610 (resistant parents) with `Spencer' (susceptible parent) to identify sources of resistance for Mi. Additionally, the RILs were evaluated in two locations in southern Illinois (Harrisburg and Dowell) in 2011 for several agronomic characteristics including yield performance. The phenotypic data collected from field and greenhouse experiments was used to select for superior lines within the two populations. The screening data was also used to identify single nucleotide polymorphism (SNP) markers associated with Mi resistance. Initial screening of the 5,361 SNP markers indicated four SNP markers (ss247062763, ss247064854, ss247077423 and ss247067293) highly associated with resistance to Mi. The results will help accelerating selection practices, and have provided high yielding resistant lines for the creation of resistant commercial varieties.

No description available.

Thesis(M.Sc.( Agriculture, Horticulture)) -- University of Limpopo, 2019 / Worldwide, tomato (Solanum lycopersicum L.) is one of the most important crops grown for nutritional value and health benefits, and are highly susceptible to root-knot (Meloidogyne species) nematodes. Following the withdrawal of synthetic chemical nematicides, Nemarioc-AL and Nemafric-BL phytonematicides have been researched and developed as alternatives to synthetic chemical nematicides. However, Nemarioc-AL and Nemafric-BL phytonematicides contains allelochemicals namely, cucurbitacin A (C32H46O9) and cucurbitacin B (C32H46O8) as their active ingredients. Therefore, the objective of this study was to determine whether increasing concentration of Nemarioc AL and Nemafric-BL phytonematicides would result in cucurbitacin residues in tomato plant, to generate mean concentration stimulation point (MCSP) values, overall sensitivity (∑k) and selected foliar mineral elements of tomato plant. Two parallel trials of Nemarioc AL and Nemafric-BL phytonematicides were conducted under field conditions, with each validated the next season. Each trial had seven treatments, namely, 0, 2, 4, 8, 16, 32 and 64% of Nemarioc-AL or Nemafric-BL phytonematicide concentrations, arranged in a randomised complete block design (RCBD), with five replications. In each trial, the seasonal interaction on variables was not significant and therefore data were pooled across the two seasons (n = 70). In both phytonematicides, the cucurbitacin residues were not detected in soil and tomato fruit. Plant variables and selected foliar nutrient elements were subjected to the Curve-fitting Allelochemical Response Data (CARD) model to generate biological indices which allowed for the calculation of MCSP of phytonematicides on tomato and their ∑k values of tomato to Nemarioc-AL and Nemafric BL phytonematicides. In Nemarioc-AL phytonematicide experiment, MCSP for tomato plant variables was at 1.13%, with the ∑k of 60 units, while the MCSP for selected tomato nutrient elements in leaf tissues was at 2.49%, with the ∑k of 21 units. Plant height, chlorophyll content, stem diameter, number of fruit, dry fruit mass, dry shoot mass and dry root mass each with increasing concentration of Nemarioc-AL phytonematicide exhibited positive quadratic relations with a model explained by 95, 82, 96, 89, 83, 83 and 92%, respectively. Similarly, K, Na and Zn each with increasing Nemarioc-AL phytonematicide concentration exhibited positive quadratic relations with a model explaining a strong relationship by 91, 96 and 89%. In Nemafric-BL phytonematicide experiment, MSCP for tomato plant variables was at 1.75%, with the ∑k of 45 units, whereas MCSP for selected tomato nutrient elements in leaf tissues was at 3.72% with the ∑k of 33 units. Plant height, chlorophyll content, stem diameter, number of fruit, dry fruit mass, dry shoot mass and dry root mass and increasing Nemafric-BL phytonematicide concentration exhibited positive quadratic relations with the model explaining a strong relationship by 92, 83, 97, 96, 87, 94 and 96%. Likewise, Na and Zn each with increasing Nemafric-BL phytonematicide concentration exhibited positive quadratic relations with a model explaining their relationship by 93 and 83%, respectively. In contrast, K with increasing Nemafric-BL phytonematicide concentration exhibited negative quadratic relations with a model explaining the relationship by 96%. In conclusion, tomato plant variables and selected foliar nutrient elements over increasing concentration of phytonematicides exhibited DDG patterns, characterised by three phases, namely, stimulation, neutral and inhibition. The developed non-phytotoxic concentration would be suitable for successful tomato production under field conditions.

No description available.

Thesis (M.Sc. Agriculture (Soil Science)) -- University of Limpopo, 2019 / Nutritional water productivity (NWP) is an assessment tool, which describes the amount of water that has been used to produce selected mineral malnutrition (MMN) elements and micronutrient malnutrition (MNMN) substances. Therefore, it links agricultural production to human nutrition. Deficiencies in MMN elements and/or MNMN substances in human nutrition referred to as malnutrition, had been linked with fatal diseases. Agricultural soils could be affected by soil-borne pathogens such as plant-parasitic nematodes, which could limit the availability of MMN elements and MNMN substances. In some communities, vegetable crops, including chilli are regarded as a major source of MMN elements and MNMN substances. Effects of root-knot (Meloidogyne species) nematodes on NWP of chilli (Capsicum annuum L.) have not been documented. The objective of the study was to determine the effects of increasing population densities of M. incognita race 2 and M. javanica on the NWP of hot chilli plants. A microplot trial was conducted at the Green Biotechnologies Research Centre of Excellence (GBRCE), University of Limpopo, South Africa. Pots were filled with 10-L steam-pasteurised (300oC) sandy clay loam soil sourced from GBRCE and Hygromix-T (Hygrotech, Pretoria North) growth medium in the ratio 3:1 (v/v). Thereafter, three-week-old hot chilli cv. 'Serrano' seedlings were transplanted into each pot, with inoculum prepared by extracting eggs and second-stage juveniles (J2) of M. incognita race 2 and M. javanica from roots of grown nematode susceptible tomato cv. 'Floradade' (Solanum lycopersicum L.) in a 1% NaOCl solution. Fourteen days after transplanting, treatments 0, 50, 125, 250, 625, 1250 and 2000 eggs and second-stage juveniles (J2) of M. incognita race 2 and M. javanica were separately inoculated using a 20 ml plastic syringe into 5-cm-deep holes in pots. At 56 days after the initiation of the treatments, Meloidogyne species xiv decreased soil pH and increased organic carbon, contributing 29 and 43% in total treatment variation (TTV) of the respective variables. Treatment effects caused the pH to decrease. NWP variables against increasing nematode numbers exhibited quadratic relations, with coefficients of determination ranging from 59 to 86% for M. incognita race 2 trial and 80 to 98% for M. javanica trial. Meloidogyne species population densities against plant variables did not show any significant relationship, except for root galling and chlorophyll content where treatments contributed 76, 98 and 47% TTV of the respective variables. Generally, root galling increased with increase in Meloidogyne species population densities, whereas chlorophyll content decreased with increasing inoculum levels. Nematode variables against their increasing population exhibited quadratic relationship with the model explained by 44 to 95% for M. incognita race 2 and 28 to 82%, association, respectively for M. javanica. In conclusion, Meloidogyne species interfered with NWP of mineral elements in chilli plant and therefore, nematode management practices should be done to reduce the nematode population densities that would confer quality to agricultural produce for human health benefits.

No description available.

Plant parasitic nematodes cause billons of dollars in annual crop losses. One of the most damaging is the root-knot nematode, Meloidogyne incognita, which is known to attack more than 3000 plants. This research will contribute to the understanding of host-plant resistance through characterization of the early infection processes of Meloidogyne incognita race 3 in susceptible (Lahontan) and resistant (Moapa) alfalfa cultivars by light microscopy and transmission electron microscopy. Neither differential penetration of M. incognita J2 into Lahontan, nor migration of J2 from Moapa, played a significant role in the resistance mechanism(s). Coiled nematodes in the cortex were observed in greater numbers in the Moapa 48 hours after inoculation. This position was interpreted as a sign of disorientation and starvation. By 96 hours after inoculation, no coiled nematodes were observed in Lahontan. In Moapa, resistance probably depends not only on the failure of the J2 to identify a suitable feeding site and initiate giant cells, but also on its inability to maintain the giant cells, once they are initiated. At the ultrastructural level, 48 hours after inoculation, the most evident change in both cultivars was the appearance of a uniform interstitial material (IM) between the nematode cuticle and the root cell wall. At 96 hours, IM in Moapa was completely agglutinated while in Lahontan it was still uniform or only slightly agglutinated. Due to these clear differences between both cultivars I propose that the IM plays a role in the resistance of Moapa to M. incognita. Immunolabeling techniques were employed to determine if the distribution of the nematode's surface coat, deposited in host tissues, differs in resistant and susceptible alfalfa cultivars. At 72 hours after inoculation, labeling of surface coat epitopes in Moapa was stronger than at 24 and 48 hours after inoculation. Labeling was observed on the nematode's cuticle, the plant cell wall, and the IM. In Lahontan, 72 and 96 hours after penetration, labeling of the surface coat epitopes was observed on the nematode's cuticle, the root cell walls, and the cell wall junctions of cells near the nematode, but not in direct contact with the cell.