Main Article Content

Authors

Entomopathogenic nematodes (EPN) are potential agents for the control of agricultural pests. Studies to improve their survival and pathogenicity under storage conditions are necessary where factors like temperature, concentration and time determine their viability. In this experiment the percent survival of nematodes (PSN) in storage was determined for six species of EPN, three steinernematids (Rhabditida: Steinernematidae): Steinernema carpocapsae (Weiser), S. glaseri (Steiner) and S. arenarium (Artyukhovsky), and three heterorhabditids: (Rhabditida: Heterorhabditidae) Heterorhabditis bacteriophora (Poinar), H. bacteriophora HP88 (Grenier) and H. baujardi LPP7 (Dolinski), at five temperatures (8, 12, 16, 20, and 24°C), two concentrations (1000 and 10000 IJ/mL) and two times (15 days and 3 months).   The experimental design was plots subdivided by time, with a 6 x 2 factorial design in the plot over two times, respectively, where each treatment had 10 replications. In the survival of all EPN, the three-way interaction among temperature, concentration and storage time was significant (P<0,05). In most of the steinernematids the PSN gradually increased in a wide range of temperature from 8 to 20°C, in both concentrations and in the shortest time, registering survival between 87 and 95%. On the contrary, high temperatures of 20 and 24°C, together with the low concentration and shortest time, favored a high survival of heterorhabditids, being between 78 and 92%, respectively. In this experiment it was possible to determine the specific conditions for each EPN that represent a high survival, for their use in programs of biological control and preservation with high viability in the laboratory.

MOLINA-ACEVEDO, J. P., MOINO-JR, A., SOUSA-CAVALCANTI, R., ANDALÓ, V., & APARECIDA MENDONÇA, L. (2006). Effect of temperature, concentration and storage time on the survival of entomopathogenic nematodes. Revista Colombiana De Entomología, 32(1), 24–30. https://doi.org/10.25100/socolen.v32i1.9354

EHLERS R. U. 1996. Current and future use of nematodes in biocontrol: Practice and commercial aspects with regard to regulatory policy issues. Biocontrol Science and Technology 6: 303-316.

FAN, X.; HOMINICK M. W. 1991. Effects of low storage temperature on survival and infectivity of two Steinernema species (Nematoda: Steinernematidae). Revue Nematologia. 14:407-412.

GEORGIS, R.; S. A. MANWEILER. 1994. Entomopathogenic nematodes: A developing biological control technology. Agriculture Zoology Review 6:63-94.

GREWAL, P.S. 2000. Anhydrobiotic potential and long-term storage of entomopathogenic nematodes (Rhabditida: Steinernematidae). International Journal for Parasitology 30, p. 995-1000.

KAYA, H. K.; STOCK, P. 1997. Techniques in insect nematology. In: Lacey, L. Manual of techniques in insect pathology. Academic Press p.281-324.

KAYA, H. K. 1990. Soil ecology. En: Entomopathogenic nematodes in biological control. R. Gaugler and H. K. Kaya (Eds.). CRC Press, Boca Raton, FL, pp. 93-115.

KAYA, H. K.; GAUGLER, R. 1993. Entomopathogenic nematodes. Annual Review of Entomology, 38:181206.

MOLINA J. P.; LÓPEZ N. J. C. 2003. Supervivencia y parasitismo de nematodos entomopatógenos para el control de Hypothenemus hampei, (Coleoptera: Scolytidae) en frutos de café. Revista Boletín de Sanidad Vegetal. Plagas 29(4): 523-533.

MOLINA J. P.; LÓPEZ N. J. C. 2001. Producción in vivo de tres entomonemátodos con dos sistemas de infección en dos hospedantes. Revista Colombiana de Entomología 27(1-2): 73-78.

MOLINEUX A. C. 1985. Survival of infective juveniles of Heterorhabditis spp and Steinernema spp (Nematoda: Rhabditida) at varies temperatures and their subsequent infectivity for insects. Review Nematology 8: 165.

SEGAL, D.; GLAZER, I. 2000. Genetics for improving biological control agents: the case of entomopathogenic nematodes. Crop Protection 19: 685-689.

SMITS, P. H. 1996. Post-application persistence of entomopathogenic nematodes. Biocontrol Science and Technology 6: 379-387.

WHITE, G. F. 1927. A method for obtaining infective nematode larvae from cultures. Science 66: 302-303.