Interaction of Endomycorrhizal Fungi,Superphosphate, and Meloidogyne incognita on Cotton in Microplot and Field Studies

Microplot and field experiments were conducted to determine the effects of two vesicular-arbuscular mycorrhizal (VAM) fungi, Glomus intraradices (Gi) and Gigaspora margarita (Gm), and dicalcium phosphate (P) on Meloidogyne incognita (Mi) reproduction and seed cotton yield of the Mi-susceptible cotton cultivar, Stoneville 213. In 1983 population densities of Mi juveniles were significantly lower 60 and 90 days after planting in microplots receiving Gi. Mycorrhizal fungi reduced the severity of yield losses to Mi, whereas P fertilization increased yield losses to Mi. In 1984 microplot yields were reduced linearly as nematode inoculum densities increased in treatments of Mi alone, Gm, or P, but the response was curvilinear with Gi. Yield suppressions in the 1984 field experiment occurred only in plots infested with Mi alone. In the 1984 microplots, numbers of Mi juveniles penetrating seedling roots increased Iinearly with increasing nematode inoculum densities and was favored when mycorrhizal fungi or superphosphate were added. Juvenile penetration of roots was negatively correlated with yields in all treatments (r = -0.54 to -0.81) except Gm and with number of bolls in Mi alone (r = -0.85) and P (r = -0.81) treatments. Mycorrhizal fungi can increase host tolerance to M. incognita in field conditions and may function as important biological control agents in soils infested with high population densities of efficient VAM species.     

Effects of Heterodera glycines and Meloidogyne incognita on Early Growth of Soybean

Greenhouse and field microplot studies were conducted to compare soybean shoot and root growth responses to root penetration by Heterodera glycines (Hg) and Meloidogyne incognita (Mi) individually and in combination. Soybean cultivars Centennial (resistant to Hg and Mi), Braxton (resistant to Mi, susceptible to Hg), and Coker 237 (susceptible to Hg and Mi) were selected for study. In the greenhouse, pot size and number of plants per pot had no effect on Hg or Mi penetration of Coker 237 roots; root weight was higher in the presence of either nematode species compared with the noninoculated controls. In greenhouse studies using a sand or soil medium, and in field microplot studies, each cultivar was grown with increasing initial population densities (Pi) of Hg or Mi. Interactions between Hg and Mi did not affect early plant growth or number of nematodes penetrating roots. Root penetration was the only response related to Pi. Mi penetration was higher in sand than in soil, and higher in the greenhouse than in the field, whereas Hg penetration was similar under all conditions. At 14 days after planting, more second-stage juveniles were present in roots of susceptible than in roots of resistant plants. Roots continued to lengthen in the greenhouse in the presence of either Mi or Hg regardless of host genotype, but only in the presence of Mi in microplots; otherwise, responses in field and greenhouse studies were similar and differed only in magnitude and variability.     

Fertilizer nitrogen budgets of two doses of Na15NO3 dressings split-applied to winter wheat in microplots on a loam soil

In a field experiment performed in microplots, winter wheat was fertilized at two different total N dressings (135 and 180 kg ha^–1) split-applied as Na¹⁵NO₃ in three equal applications at tillering, stem elongation, and flag leaf.No significant differences were found in the percentage recovery values for the entire plant at the three split applications between the two N dressings. The total percentage recovery of fertilizer N by the plant was high and practically equal at both fertilization levels (76.65% and 75.84% for 135 and 180 kg N ha^–1, respectively); crop yields were also similar. In contrast, gaseous losses calculated after drawing up the balance sheet were, in absolute values, higher for the tillering and stem elongation split applications when using the 180 kg N ha^–1 dressing (7.67 and 4.84 kg N ha^–1, respectively) than for the 135 kg N ha^–1 dressing (3.45 and 1.26 kg N ha^–1, respectively). They were found to be zero at flag leaf at both fertilization levels. The amount of applied fertilizer N did not influence the amount of N taken up from the soil which was about 143 kg ha^–1.     

Fertilizer and soil nitrogen accumulation by irrigated barley grown on a red-brown earth in south-eastern Australia

¹⁵N labelled (NH₄)₂SO₄ was applied to barley at 5 g N m⁻² (50 kg N ha⁻¹) in microplots at sowing to study the timing of the N losses and the contribution of soil and fertilizer N to the plant. Water treatments included rainfed and irrigation at 45–50 mm deficit beginning in the spring. Recovery of¹⁵N in the plant increased to a maximum of about 20% within 91 days after sowing (DAS 91) and then remained constant. Approximately 16% (0.8 g N m⁻²) of the fertilizer was in the stem and leaves at DAS 91 and this N was subsequently redistributed to the head. At maturity, approximately 75% of the¹⁵N assimilated by the tops was recovered in the grain. Soil N contributed 3.6 g N m⁻² to the head; 2.2 g N m⁻² was remobilized from the stem and leaves, and the balance, approximately 1.4 g N m⁻², was taken up from the soil between DAS 69 to 91. Effects of irrigation treatments on N accumulation were not significant. Residual¹⁵N fertilizer in the soil decreased with time from sowing, and at maturity 40% of the applied N was recovered in the surface 0.15 m.¹⁵N movement to depth was limited and less than 5% of the fertilizer was recovered below 0.15 m. Irrigation had no effect on the¹⁵N recovery at depth. Total recovery of the¹⁵N varied between 60 and 67% and implies that 33–40% was lost from the soil-plant system. The total recovery in the soil and plant was not affected by time or irrigation in the interval DAS 39 to 134. Losses occurred before DAS 39 when crop uptake of N was small and soil mineral N content was high. There was an apparent loss of 1.9 g fertilizer N m⁻² (i.e. 38% of that applied) between DAS 1 and 15. This loss occurred before crop emergence when rainfall provided conditions suitable for denitrification.     

Fertilizer nitrogen budget of Na15NO3 and (15NH4)2SO4 split-applied to winter wheat in microplots on a loam soil

Labelled fertilizer N applied to winter wheat as Na¹⁵NO₃ and (¹⁵NH₄)₂SO₄ at a total N dressing of 100kg ha⁻¹ was used in a microplot balance study to investigate the fate of each split fraction at three growth stages: end of tillering, heading and beginning of flowering. Results indicated that while the percentage utilization of the applied N by the grain and total crop increased considerably from the first to the third split application, these values diminished steadily in the straw. Grain recovery values for the first, second and third split applications were 34.2%, 51.5% and 55.7% for the NO₃ and 32.3%, 48.4% and 52.5% for the NH₄ carrier, respectively. The corresponding recovery values for the whole plant were 54.6%, 67.8% and 69.9% for the NO₃ and 51.7%, 63.5% and 66.1% for the NH₄ carrier. A greater proportion of the fertilizer N applied at the end of tillering stage was found in the vegetative plant components as compared with the grain. The reverse occurred for the N applied at the heading and at the beginning of the flowering stages. The residual fertilizer N found in the soil amounted to 18.0%, 10.4% and 11.6% of the applied NO₃−N and to 22.5%, 12.7% and 15.2% of the applied NH₄−N for the respective split applications. No differences were found for each split application between the two carriers as far as the unaccounted fertilizer N was concerned. The losses were 26.6%, 22.3% and 18.6% of the applied N for the three split applications, respectively. The application of fertilizer N did not lead to any increase in soil N uptake by the crop.     

Response of Resistant Soybean Plant Introductions to Meloidogyne arenaria Races 1 and 2

Resistant plant introductions, PI 230977 and PI 200538, and partially resistant Jackson and susceptible CNS were evaluated for seed yield in response to races 1 and 2 of Meloidogyne arenaria. Initial soil population densities (Pi) of the nematode were 0, 31, 125, and 500 eggs/100 cm³ soil. At the highest Pi, yield suppressions of CNS, Jackson, PI 230977, and PI 200538 were 55, 28, 31, and 29%, and 99, 86, 66, and 58% for races 1 and 2 compared with uninfested controls. Numbers of second-stage juveniles (J2) present in roots 14 days after planting increased as Pi increased, but did not differ between the two races. At the highest Pi, fewer race 1 (40-57%) and race 2 (53-68%) J2 were present in roots of the plant introductions than in roots of Jackson. Soil population densities of race 1 J2 at 135 days after planting were 83-89% lower on the resistant genotypes than on CNS. These numbers did not differ for race 2. Reproductive factors were considerably higher for race 2 compared to race 1 for all genotype by Pi combinations, except for CNS at the highest Pi.     

Efficacy of Bacillus thuringiensis,Paecilomyces marquandii,and Streptomyces costaricanus with and without Organic Amendments against Meloidogyne hapla Infecting Lettuce

Chitin, wheat mash, or brewery compost were incorporated into unfumigated and methyl bromide-fumigated organic soils placed in microplots formed from cylindrical drainage tiles (0.25 m-diam. clay tile). After 3 weeks, Meloidogyne hapla and cell or spore suspensions of Bacillus thuringiensis, Paecilomyces marquandii, and Streptomyces costaricanus were individually added to the soils of designated microplots. A B. thuringiensis + S. costaricanus combination was also tested. Lettuce seedlings, cv. Montello, were transplanted into the soils 3 to 4 days later. All the bacterial and fungal antagonists applied without a soil amendment, except the B. thuringiensis + S. costaricanus treatment, reduced root galling and increased lettuce head weight in the unfumigated organic soil, but not in the fumigated soil. All three amendments were also effective against M. hapla and reduced root galling in fumigated and unfumigated soils. Wheat mash amendment increased lettuce head weight in the unfumigated soil. In general, no antagonist × amendment interaction was detected. Soil populations of B. thuringiensis were maintained at ≥4.0 log10 colony-forming units/g organic soil during the first 14 days after planting. However, viable cells of B. thuringiensis were not detected after 49 days.     

Relationship Between Population Densities of Pratylenchus penetrans and Crop Losses in Flue-Cured Tobacco in Ontario

Flue-cured tobacco was grown in microplots consisting of concrete drainage tries, 40-cm (i.d.), infested with 0; 666 ; 2000; 6000 or 18,000 root-lesion nematodes, Pratylenchus penetrans/kg of soil. Yield and grade index decreased with preplant soil population densities in excess of 2000/kg of soil. At initial densities of 6000 and 18,000/kg of soil losses in crop returns were 11.0% and 27.5%, respectively. Decreases in the maturity index and in percentage dry stalk weight with increasing densities showed that the nematode delayed maturity. Increases in population densities of nematodes were correlated with decreases in weights of tops and roots and in plant height. All final population densities in soil were lower than the initial densities except at the lowest pre-plant density. All soil populations at midseason were lower than those at the beginning and end of the growing season. Populations of P. penetrans at harvest were in excess of half a million per root system with the 18,000/kg initial soil population density. The results suggest that fumigation, which costs $75/ha, or approximately 2% of the crop value, is economically warranted at preplant densities in excess of 2000/kg of soft.     

Influence of Planting Date on Population Dynamics and Damage Potential of Pratylenchus brachyurus on Soybean

Planting date was used as a variable to determine the effects of time and different environmental conditions on the population dynamics and damage potential of Pratylenchus brachyurus on soybean at two locations in North Carolina. An initial population slightly less than the damage threshold (275 nematodes/500 cm³ soil) was used to minimize the influence of host damage on this nematode''s population dynamics and to gain greater precision in characterizing factors which influence the damage potential of P. brachyurus to soybean. Equivalent nematode numbers generally resulted in greater yield suppression of soybean in early plantings. Early planting of soybean also resulted in greater (P = 0.01) population densities of P. brachyurus at midseason which often persisted until soybean harvest. Length of time for reproduction and intraspecific competition occurring when soybeans were stunted by the nematode were the most important factors influencing the population dynamics of P. brachyurus.