Effect of Meloidogyne incognita on Plant Nutrient Concentration and Its Influence on the Physiology of Beans.

Phaseolus vulgaris plants, 3, 8, 11, and 13 days old, were inoculated with 0, 2,000, 4,000, or 8,000 second-stage Meloidogyne incognita larvae and maintained under controlled conditions. The photosynthetic rate and the shoot and root concentration of K, Ca, Mn, Fe, Cu, and Zn were determined by destructive assay at 1-27-day intervals and by nondestructive assay of leaves, stems, and roots at 27 or 28 days after inoculation. In the destructive assay, the concentration of the elements in the plant tissues did not change until 1 week after inoculation. Thereafter, the trend was mostly decreasing for shoot K and Fe and increasing in the root, whereas Ca had the opposite trend in the shoots. Manganese, Cu, and Fe showed variable trends. Generally, the concentration of K and Mn increased, whereas Ca and Fe decreased, with duration of infection in all treatments. Zinc and Cu decreased in the highest nematode treatments. The overall elemental content generally decreased with level of infection from 1 week after inoculation. Photosynthetic rate based on shoot K concentration significantly decreased with level of infection. In most of the nondestructive assays, the concentrations of shoot K, Zn, and Mn decreased, whereas Ca increased with increasing nematode treatment. One of the first effects of the nematode on host physiology appears to be a change in concentration of nutrient elements in the host plant.

[1]  H. Melakeberhan,et al.  Relationship between physiological response of French beans of different age to Meloidogyne incognita and subsequent yield loss , 1986 .

[2]  N. Hague,et al.  The effect of Heterodera avenae, on the root system of susceptible and resistant oat seedlings , 1986 .

[3]  J. D'auria,et al.  The influence of Meloidogyne incognita on the growth, physiology and nutrient content of Phaseolus vulgaris , 1985 .

[4]  K. Torimitsu,et al.  Effect of K+ and H+ stress and role of Ca2+ in the regulation of intracellular K+ concentration in mung bean roots , 1985 .

[5]  H. Melakeberhan,et al.  Response of phaseol us vulgaris to a single generation of meloidogyne incognita , 1985 .

[6]  I. Ferguson Calcium in plant senescence and fruit ripening , 1984 .

[7]  D. Clarkson Calcium transport between tissues and its distribution in the plant , 1984 .

[8]  J. Sanderson,et al.  The translocation of calcium from oat roots infected by the cereal cyst nematode Heterodera avenae (Woll.) , 1984 .

[9]  M. Hassan,et al.  Effect of Root-Knot Nematodes On the Mineral, Amino Acid and Carbohydrate Concentrations of Almond and Peach Rootstocks , 1980 .

[10]  J. Popham,et al.  Monitoring trace elements in the mussel, Mytilus edulis using X-ray energy spectroscopy , 1979 .

[11]  K. Evans,et al.  Tolerance to cyst-nematode attack in commercial potato cultivars and some possible mechanisms for its operation , 1979 .

[12]  H. R. Wallace,et al.  Changes in free proline following infection of plants with either Meloidogyne javanica or Agrobacterium tumefaciens , 1978 .

[13]  N. J. Brown,et al.  Effects of Potato Cyst-Nematodes On Potato Plants , 1975 .

[14]  R. E. Paulson,et al.  Giant cell formation in tomato roots caused by Meloidogyne incognita and Meloidogyne hapla (Nematoda) infection. A light and electron microscope study , 1970 .

[15]  K. G. Parker,et al.  Effect of phosphorus and potassium nutrition of sour cherry on the soil population levels of five plant-parasitic nematodes. , 1964 .

[16]  R. Cory,et al.  Translocation of Calcium in the Bean Plant. , 1959, Plant physiology.

[17]  A. H. Hunter NUTREENT ABSORPTION AND TRANSLOCATION OF PHOSPHORUS AS INFLUENCED BY THE ROOT KNOT NEMATODE (MELOIDOGYNE INGOGNITA ACRITA) , 1958 .