Expression of resistance to Meloidogyne incognita and M. javanica from Aegilops squarrosa was studied in a synthetic allohexaploid produced from Triticum turgidum var. durum cv. Produra and Ae. squarrosa G 3489. The reproductive rate of different races of M. incognita and M. javanica, expressed in eggs per gram of fresh root, was low (P < 0.05) on the synthetic allohexaploid and the resistant p...

The antagonistic effects of raw sewage sludge on infection of tomato by Meloidogyne incognita were tested in greenhouse pot experiments. Sludge was mixed with the soil or added on its surface before and after inoculation of tomato plants with nematode eggs. Juvenile penetration was determined 1 and 10 days after inoculation, and 6 weeks later root systems were assessed for nematode reproduction...

The tethered-nematode technique was adapted for use with second-stage juveniles of Meloidogyne incognita. The data demonstrate that M. incognita exhibits the same patterns of behavior as adults of the free-living nematode, Caenorhabditis elegans. The principal differences are that M. incognita is slower and less regular in its behavior than C. elegans. The frequency of normal waves is about 0.2...

Seedlings of Corchorus capsularis (cv. C4444) were inoculated with Meloidogyne incognita, Hoplolaimus indicus, and a fungus pathogen of jute, Macrophomina phaseoli, separately and in all possible combinations. The significant damage of jute plants caused individually by the pathogens was aggravated when the fungus was associated with either of the nematode species. M. incognita alone caused gre...

Meloidogyne incognita wartellei n. subsp, is described and illustrated from roots of soybean (Glycine max L.) near Washington, Louisiana. It is rather limited in distribution in that state, being known at five locations comprising about 60,000 acres. It not only attacks commonly susceptihle soybeans but is a destructive pest on other commercial soybean varieties that are resistant to other form...

Rates of penetration and development ofMeloidogyne incognita race 4 in roots of resistant (inbred Mp307, and S4 lines derived from the open-pollinated varieties Tebeau and Old Raccoon) and susceptible (Pioneer 3110) corn genotypes were determined. Seedlings grown in styrofoam containers were inoculated with 5,000 eggs of M. incognita. Roots were harvested at 3-day intervals starting at 3 days a...

field experiments were conducted to determine the optimum application rate of sunn hemp crotalaria juncea leaf residue in the management of meloidogyne incognita on tomato. sunn hemp applied at rates of 0 (control), 2, 4 and 6 kg/ha showed a varied effect on second stage juveniles of m. incognita. there were no differences in plant height and stem girth. the 6 kg/ha treatment reduced the m. inc...

The effects of soil temperature and initial inoculum density (Pi) of Meloidogyne incognito and M. javanica on growth of wheat (Triticum aestivum cv. Anza) and nematode reproduction were studied in controlled temperature baths in the glasshouse. Nematode reproduction was directly proportional to temperature between 14 and 30 C for M. incognita and between 18 and 26 C for M. javanica. Reproductio...

A total of 1,256 populations of Meloidogyne incognita and 442 populations of M. arenaria were collected from vegetables in eight districts of Uttar Pradesh, India. Host differentials were used to identify the host race of each population. All four host races of M. incognita were present in six of the eight districts. In the other two districts, only host races 1, 2, and 4 were found. Although f...

The effects of nematicides carbofuran (C) and fenamiphos (F) and herbicides metribuzin (M) and trifluralin (T), alone and in combination, on hatching, penetration, development, and reproduction of Meloidogyne incognita race 3 were determined under laboratory conditions. To study hatching, entire egg masses were exposed to nematicides (6 mug/ml), herbicides (0.5 mug/ml), and their combinations o...