,  , The nematicidal and egg haching inhibitory effects of extracts from 30 herbal plants (total 32 samples) against Meloidogyne hapla J2 juveniles and eggs was tested using the dipping method. At 1,000 ppm, extracts of Daphne genkwa flower buds, Eugenia caryophyllata flowers, Quisqualis indica fruits, and Zingiber officinale rhizomes produced >, 80% mortality in J2 juveniles. At 125 ppm, extracts of D. genkwa and Q. indica produced 91 and 99% mortality, respectively. The toxicity of 5 selected plant extracts to M. hapla differed depending on the solvent used (i.e. hexane, methanol, hot water, or cold water). Hot water extracts of Z. officinale and Q. indica produced nematicidal efficacies of99 and 99%, compared to 36 and 98%, respectively, with cold water extraction. Q. indica extract was highly active against M. hapla regardless of extraction method. The inhibitory effects of Areca catechu, D. genkwa, Desmodium caudatum, Pharbitis nil, Q. indica, and Z. officinale extracts on egg hatching of M. hapla was evaluated. At 1,000 ppm, D. genkwa, P. nil, and Q. indica extracts significantly reduced hatching at 7, 14 and 21 days after treatment. Numbers of juveniles in soil treated with the methanol extract

The toxicity of Kaempferia galanga rhizome materials and constituents against Meloidogyne incognita second‐stage juveniles (J2) and eggs were examined. The active principles of K. galanga rhizome were identified as the phenylpropanoids ethyl (E)‐cinnamate (EC, 1) and ethyl (E)‐p‐methoxycinnamate (EMC, 2) by spectroscopic analysis. Results were compared with those of carbofuran, fosthiazate, and metam‐sodium. In direct‐contact mortality bioassay, EC (LC50, 0.037 mg/ml) was the most toxic constituent, followed by EMC (0.041 mg/ml). EC was more effective than carbofuran (LC50, 0.092 mg/ml) but less active than fosthiazate (0.002 mg/ml). EC, egg hatch was inhibited 100, 93, and 87% at 125, 62.5, and 31.25 μg/ml, respectively. EMC caused 100, 81, and 75% inhibition of egg hatch at 125, 62.5, and 31.25 μg/ml, respectively. The inhibition of two phenylpropanoids were similar or more inhibition to that of either carbofuran or metam‐sodium but was lower than that of fosthiazate. In contact + fumigant mortality bioassay, EC and EMC treatments resulted in 86 and c 73% mortality at 0.5 and 0.125 mg/g soil, respectively. The lethality of these phenylpropanoids was almost similar to that of either carbofuran or metam‐sodium but was lower than that of fosthiazate. In vapor‐phase mortality bioassay, EC and EMC were more effective in closed container than open containers, indicating that the mode of delivery of these compounds was, in part, a result of vapor action. K. galanga rhizome‐derived materials, merit further study as potential nematicides and hatching inhibitors for the control of M. incognita populations.

The toxicity of Kaempferia galanga rhizome-derived methanol extract (RME), powder (RP) and steam distillate (RSD) to Meloidogyne incognita second-stage juveniles (J2) and eggs and their effects on Lycopersicon esculentum germination and growth were examined in vitro and in pot experiments. Results were compared with those of three nematicides. In contact+fumigant bioassays with J2, RME applied at 1, 0.5 and 0.25mg/g soil exhibited 92, 88, and 73% mortality, respectively. The lethality of RME was almost similar to that of carbofuran but lower than that of either fosthiazate or metam-sodium. RSD and RP were less active than RME. In vapor-phase mortality bioassayswith J2, the test materials were effective in closed container than in open one, indicating that mode of delivery was, in part, a result of vapor action. RME, RSD, and fosthiazate treatments resulted in 91, 100, and 95% inhibition of egg hatch at 250μg/ml and 82, 88, and 81% inhibition of egg hatch at 100μg/ml, respectively. In filter-paper bioassays with L. esculentum seed at 8.8μg/cm2, RME and RP did not cause germination inhibition, while RSD and fosthiazate treatments resulted in 84 and 13% germination inhibition. In pot tests, RME and RSD applied at 8mg/g soil reduced galling caused by M. incognita significantly and fosthiazate at 0.02mg/g soil reduced galling completely. Rhizome materials did not cause any adverse effect on growth of L. esculentum, while fosthiazate application caused significantly reduced root weight. K. galanga rhizome-derived materials, particularly methanol extract, merit further study as potential nematicides and hatching inhibitors for the control of M. incognita populations as fumigants with contact action.