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1 September 2003 PATHOGENS AND PARASITIC NEMATODES ASSOCIATED WITH POPULATIONS OF FALL ARMYWORM (LEPIDOPTERA: NOCTUIDAE) LARVAE IN MEXICO
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Abstract

Larvae of fall armyworm (FAW), Spodoptera frugiperda (J. E. Smith) and soil samples were collected in six Mexican states. Larvae were collected from whorl-stage corn, grain sorghum, forage sorghum, and Sudan grass fields in 64 locations during the summer of 2000, to determine the occurrence of entomopathogens and parasitic nematodes. A total of 5591 FAW larvae from 64 locations were examined for indigenous FAW biological control agents. Overall total larval mortality was 3.935%. The larval mortality percent due to entomopathogens and parasitic nematodes was 3.524%, other causes reached 0.411% of total mortality. Three species of entomopathogenic fungi representing two classes, Hyphomycetes (Nomuraea rileyi, and Hirsutella sp.) and Zygomycetes (Entomophthora sp.) were recovered from FAW larvae, and two species of Hyphomycetes (Metarhizium anisopliae and Beauveria bassiana) were isolated from soil samples. An unidentified microsporidian was recovered from four locations in the State of Jalisco, three from Michoacán, three from Nayarit, and one from Veracruz and Colima, respectively. Mermithid nematodes were recovered from 24 FAW larvae at three locations in Nayarit and three larvae were recovered from two locations in Veracruz. Six larvae showing symptoms of viral disease were collected from Sinaloa (2), Jalisco (2), Michoacán (1), and Nayarit (1). Entomopathogenic nematodes from the genus Heterorhabditis sp. and Steinernema sp. were isolated from soil samples from Colima in one and two locations, respectively. Steinernema sp., and Heterorhabditis sp. were isolated from soil in one location in Michoacán. Steinernema sp. was recovered from two locations of Jalisco. In this survey, N. rileyi, mermithid nematodes, and microsporidia were the most frequent pathogens and parasites.

The fall armyworm (FAW), Spodoptera frugiperda (J. E. Smith), causes considerable economic losses in maize, sorghum, peanuts, cotton, soybeans and occasionally other crops, in most of the countries of the Western Hemisphere (Sparks 1986). Control of this pest is usually achieved through the application of synthetic insecticides (Hruska & Gould 1997), but their high cost, environmental contamination, development of resistance to chemicals, and pest resurgence (Colborn 1995; Crowe & Booty 1995) have encouraged the search for alternatives more compatible with the environment. Microbial control is an environmentally sound and a valuable alternative to the use of chemicals for controlling this pest.

Interactions between insect host, environment, insect host age (Fuxa et al. 1988; Molina-Ochoa et al. 1996), pathogens and plant to be protected (Bergman & Tingey 1979; Hamm & Wiseman 1986; Barbercheck 1993; Wiseman & Hamm 1993; Molina-Ochoa et al. 1997, Molina-Ochoa 1999) determine the strategies for using pathogens in microbial control (Hamm 1984). FAW larvae are susceptible to entomopathogenic bacteria, fungi, nematodes, protozoa, and viruses (Gardner & Fuxa 1980; Agudelo-Silva 1986; Hamm et al. 1986; Patel & Habib 1988; Richter & Fuxa 1990; Lezama-Gutierrez et al. 1996; Molina-Ochoa et al. 1996; Molina-Ochoa et al. 1999). The insect host age, habitat and soil type, pesticide use, agricultural practices, and location, influence the natural distribution of biological control organisms (Croft & Brown 1975; Fuxa 1982; Agudelo-Silva 1986; Hamm et al. 1986; Sosa-Gomez & Moscardi 1994; Vanninen 1996; Chandler et al. 1997; Mietkiewski et al. 1997;Molina-Ochoa et al. 2001).

As a result of economic and environmental concerns, surveys for natural enemies of the FAW occurring in Mexico have been conducted to develop a better understanding of the pathogen complex, parasitic nematodes and parasitoids (Lezama-Gutierrez 2001, Molina-Ochoa 2001, Molina-Ochoa et al. unpublished). These two surveys conducted in four Mexican states reported the occurrence of the fungi Beauveria bassiana, Nomuraea rileyi, and Hirsutella sp., an unidentified microsporidian, mermithid nematodes, and an ascovirus affecting FAW larvae. The occurrence of the bacterium Bacillus thuringensis and steinernematid and heterorhabditid nematodes are reported from soil samples.

This paper reports on the presence of entomopathogens and parasitic nematodes in FAW larval populations and recovered from soil samples of corn, grain sorghum, forage sorghum, and Sudan grass fields from six Mexican states, during the summer of 2000.

Materials and Methods

Isolation of Entomopathogens from FAW Larvae

During August and September of 2000, FAW larvae were collected from whorl-stage corn, grain and forage sorghum, and Sudan grass fields in 64 locations in the Mexican states of Sinaloa, Nayarit, Jalisco, Colima, Michoacán, and Veracruz. Concurrently, four soil samples were obtained from each location in all of the states. Location 43 comprised a combination of collections from adjacent corn and grain sorghum field in whorl-stage. Sample size ranged from 33 to 119 FAW larvae per field, but most often sample size was about 90. The number collected was corrected by subtracting the number that died from injury or unknown causes during the first days after collection. Collection data and percent infection by entomopathogens and parasitic nematodes is presented in Table 1. Larval mortality due to insect parasitoids is reported elsewhere (Molina-Ochoa et al., in press).

Larvae were placed individually in 30 cc plastic cups with regular pinto bean diet (Burton & Perkins 1989) and maintained in the laboratory to record the larvae infected by entomopathogens and parasitic nematodes. Mermithid nematodes that emerged from larvae were collected and placed in crystal vials containing 2 ml of 70% ethanol. Dead FAW larvae showing signs of fungal infection were placed in plastic Petri dishes (60 × 10 mm) lined with a piece of 5.5 cm-diameter filter paper (Whatman No. 1) moistened with sterile distilled water until the fungus sporulated on the insect surface. A medium composed of 200 ml of V8 vegetable juice, 5 g glucose, 2 g yeast extract, 3 g CaCO3, 15 g agar, and 800 ml distilled water (Fargues & Rodriguez-Rueda 1980) for isolating the fungus Nomuraea rileyi was used. A Sabouraud-dextrosa-agar medium enriched with 1% (w/v) yeast extract (SDAY), and 500 ppm chloramphenicol (Lezama et al. 1996) for growing other fungus species was used. Entomophthorales were not isolated.

Isolation of Entomopathogenic Fungi and Nematodes from Soil

In each location of the six surveyed states, a 2 kg combined soil sample was collected. A soil sub-sample, about 500 g from four different points a few meters apart, was obtained by digging to a depth of 10-15 cm with a small shovel. Soil samples were deposited into double plastic bags, tagged, stored in a plastic cooler, and taken to the laboratory where they were kept at 25°C until processing. The storage time ranged from a few days to three weeks. Soil was thoroughly mixed and passed through a 0.4 mm mesh sieve, breaking soil lumps and separating any litter.

For isolating entomopathogenic nematodes and fungi, greater wax moth (GWM) larvae, Galleria mellonella L., were used as bait (Bedding & Akhurst 1975; Tarasco et al. 1997). From the 2 kg combined soil sample from each location, two samples were placed in 1000 ml capacity plastic pots and five GWM last instar larvae were released into each pot. Pots were incubated at 25°C in the dark for a 10-day period (Woodring & Kaya 1988, Bidochka et al. 1998). Larval cadavers were removed and surface-sterilized with 1% Sodium hypochlorite for a 3 minute-period, then washed three times with sterile distilled water and placed on damp filter paper in a 60 mm diameter sealed Petri dish, and incubated at 25°C for 12 days (Chandler et al. 1997). Entomopathogenic fungi from the larvae were isolated using SDAY, with 500 ppm of chloramphenicol (Lezama-Gutierrez et al. 1996). Fungi were identified by microscopic inspection of morphological characteristics in situ or after isolation in SDAY according to the criteria by Brady (1979) and Samson et al. (1988).

The entomopathogenic nematodes were separated to genera by identifying coloration of Galleria cadavers according to Woodring & Kaya (1988).

Entomopathogenic viruses and bacteria from FAW larvae and soil, respectively, have not been yet isolated or identified.

Geographical Coordinates and Collection Data

A Garmin GPS III Plus™ was used for obtaining the coordinates and altitude data. Location, date, place, coordinates, altitude, crop, sample size, and percentage of infected larvae are shown in Table 1.

Results

In this survey, out of 5591 FAW larvae collected from 64 locations in six Mexican states, the entomopathogens and parasitic nematodes killed 197 larvae. Overall larval mortality percentage due to these organisms was 3.524%. Mortality percentage per location ranged from 0.000 to 44.444% (Table 1). Considering the total mortality due to entomopathogens and parasitic nematodes, 137 (69.54%) larvae were killed by entomopathogenic fungi, 26 (13.19%) larvae were killed by microsporidia, six (3.04%) larvae were killed by viruses, and 28 (14.21%) larvae were killed by mermithid nematodes. Two classes of entomopathogenic fungi were collected. The class Zygomycetes was represented by Entomophthora sp. which infected a larva from Colima and a larva from Veracruz. The class Hyphomycetes was represented by Nomuraea rileyi and Hirsutella sp. which infected 134 and one larvae, respectively. N. rileyi was responsible for 68.020% of total mortality due to entomopathogens and parasitic nematodes, and was the most abundant and widely distributed, occurring in all the states. Hirsutella sp. occurred in Sinaloa, only. Mermithids were collected from the states of Nayarit (23), and Veracruz (5), only, and accounted for approximately 14.21% of total mortality of FAW larvae.

The 26 FAW larvae infected by microsporidia were collected in five of six states sampled (Michoacán (10), Nayarit (9), Jalisco (5), Colima (1), Veracruz (1) and Sinaloa (0)). These entomopathogens accounted for 13.19% of the total FAW larval mortality. The symptoms of larvae infected with these entomopathogens were similar to the unidentified microsporidia reported by Lezama-Gutierrez et al. (2001). They often were dry and fragile when dead, resembling cigarette ashes. Few FAW larvae showed symptoms of ascovirosis infection (Hamm et al. 1986). Two were detected in Jalisco in one location, two in two separate locations in the same municipality in Sinaloa, one in Michoacán, and one in Nayarit. The viruses were not identified by electron microscopy. The percentage of fall armyworm larvae infected by pathogens and parasitic nematodes at each location is shown in Table 2.

Entomopathogens Isolated from Soil

Two species of entomopathogenic fungi, Metarhizium anisopliae and Beauveria bassiana, were recovered from 10 of 64 soil samples. M. anisopliae was recovered from four of eleven locations in Colima, and in one location in each of Nayarit, Jalisco, and Michoacán. Beauveria bassiana was recovered from two locations in Veracruz and one in Michoacán.

Two genera of entomopathogenic nematodes, Steinernema sp., and Heterorhabditis sp. were collected from soil samples. Steinernematid nematodes were recovered from five of 64 locations (two locations in Colima, two in Jalisco, and in one in Michoacán). Heterorhabditid nematodes were recovered in two locations, one in Colima and one in Michoacán.

Discussion

Current research efforts are focused on selecting native and exotic entomopathogens, which are highly virulent to arthropod pests, for developing efficient and environmentally-sound bioinsecticides. The high susceptibility of fall army-worm larvae and other lepidopterous pests to strains of N. rileyi, B. bassiana and M. anisopliae has been demonstrated (Bustillo & Posada 1986; Habib & Patel 1990; Lecuona & Lanteri 1999). N. rileyi has been reported infecting FAW larvae naturally in Brasil (Valicente 1989), Venezuela (Agudelo-Silva 1986), Puerto Rico (Pantoja et al. 1985), Colombia (Vargas & Sánchez 1983), United States (Fuxa 1982), Mexico (Lezama-Gutiérrez et al. 2001), and other countries. In this survey, N. rileyi caused 68.020% of the total FAW larval mortality due to pathogens and parasitic nematodes, and was the most abundant and widely distributed entomopathogen, occurring in each of the six states surveyed. Similar results were reported by Lezama-Gutiérrez et al. (2001) from a survey conducted in Colima, Jalisco, and Michoacán.

Entomophthora aulicae was reported attacking FAW larvae on grain sorghum in Georgia (Hamm 1980; Schwehr & Gardner 1982), and Argentina (Vera et al. 1995). Entomophthora sp. and Hirsutella sp. were reported attacking larvae of this pest with parasitism rates that ranged from 0.6% to 1.1%, respectively (Lezama-Gutiérrez et al. 2001). In this study, parasitism rates for E. sp., and H. sp. were 3.030 and 1.520%, respectively. Total FAW mortality caused by all the pathogens was 3.524% (197 larvae killed).

An unidentified microsporidian was the third cause of FAW total larval mortality with 13.19%, and was similar to that reported by Lezama-Gutierrez et al. (2001). Most larvae infected with the microsporidian were collected from Michoacán, Nayarit, and Jalisco, with 10, 8, and 5 infected larvae, respectively. The arrangement of the spores of this microsporidian suggested that this entomopathogen was neither Nosema nor Vairimorpha as previously reported by Gardner & Fuxa (1980).

A few larvae showed symptoms and signs similar to those from ascoviruses, but the identity of these viruses was not verified by electron microscopy. Occurrence of entomopathogenic viruses has been reported in Latin America, in Puerto Rico, Argentina, Brasil, and Mexico (Valicente 1989; Pantoja & Fuxa 1992; Vera et al. 1995; Lezama-Gutierrez et al. 2001).

In this survey, the mermithid nematodes were important natural enemies of FAW larvae. They were the second most important mortality factor, causing 14.21% of total mortality. Nematodes from the genus Hexamermis have been reported attacking FAW larvae in Honduras, Brasil, Nicaragua, and Argentina (Van Huis 1981; Valicente 1989; Wheeler et al. 1989; Vera et al. 1995). Mermithids attacking FAW larvae in Mexico were reported by Alcocer-Gómez & Méndez-Villa (1965). They found parasitism ranging from 8 to 100% during a 3-year study. An association between the pest density and percent of parasitism was determined. Rainfall also was cited as an important factor in influencing percent parasitism. In a recent survey conducted in Mexico, mermithid nematodes caused larval mortality ranging from 0.0 to 14.9% in Colima (Lezama-Gutierrez et al. 2001). But in our survey, mermithids were not recovered in Colima. However, similar percentages of mortalities were recorded (0.000 to 15.054%) from other locations, with the highest rate of parasitism from Nayarit and Veracruz. A possible reason for the difference between the findings of Lezama-Gutierrez et al. (2001) and those we report is that most of the locations in Colima were different than those sampled by Lezama-Gutierrez et al. (2001) during the summer of 1998.

The entomopathogenic fungi and nematodes were recovered in 26.5% of the soil samples (17 of 64 locations). M. anisopliae and B. bassiana were isolated in 15.6% of the samples. They occurred in Colima, Michoacán, Nayarit, and Veracruz, but were not found in Jalisco and Sinaloa. M. anisopliae was recovered from five locations in Colima, and one location each in Michoacán and Nayarit. B. bassiana was recovered in two locations of Veracruz and one location in Michoacán. In a study conducted in Szczecin, Poland using soils collected from forests during the spring and autumn, the entomopathogenic fungi M. anisopliae and B. bassiana infected wax moth larvae (Mietkiewski et al. 1998), and M. anispoliae was the dominant species. Recently, Lezama-Gutierrez et al. (2001) reported three species of entomopathogenic fungi recovered from soil samples using the Galleria technique; M. anisopliae, B. bassiana, and Paecilomyces fumosoroseus, with M. anisopliae being the most dominant species. In our soil samples, M. anisopliae was also the most dominant, occurring in 10.9% of the locations, while B. bassiana occurred only in 4.7% of the locations (Table 3).

Steinernematid and Heterorhabditid nematodes were found in seven of 64 locations (10.9%). Steinernematid nematodes were recovered from Colima in two locations, one in Michoacán, and two in Jalisco. Heterorhabditids occurred in Colima and Michoacán, in one location, respectively. Low rates of entomopathogenic nematode recovery have been reported in different regions around the world, and range from 3.9% to 21.4% (Constant et al. 1998; Tangchitsomkid et al. 1998; Griffin et al. 2000; Rosa et al. 2000; Lezama-Gutierrez et al. 2001). Soil pH and type, altitude, habitat, soil temperature, croplands, orchards, pastures, and proximity to coastal lands were discussed as possible factors affecting the occurrence of these entomopathogens.

The diversity and distribution of entomopathogens and parasitic nematodes occurring in Mexico could play an important role in regulating the FAW larval populations. Additional research is needed on the identification, biology, and potential of the microsporidia frequently recovered in the surveys conducted during 1998 and 2000. There is also a need to identify the role of mermithid nematodes as potential biological control agents. Additional research has already been conducted at the Universidad de Colima, Mexico, to identify the steinernematid and heterorhabditid nematodes isolated, and to determine their potential for biological control of fall armyworm larvae and other lepidopterous pests.

Acknowledgments

This work was supported by funds from Universidad de Colima, Mexico, we thank Dr. Carlos Salazar Silva, Rector of this institution. The authors express their gratitude to Dr. J. J. Hamm, and Dr. R. E. Lynch (USDA-ARS, Crop Protection and Management Research Unit, Tifton, GA) for their assistance and identification of the pathogens. We also thank Dr. J. E. Foster, Dr. E. A. Heinrichs (University of Nebraska Lincoln, Lincoln, NE), and Dr. S. R. Skoda (USDA-ARS, Midwest Livestock Insects Research Laboratory, Lincoln, NE) for review of the manuscript. We recognize J. J. Molina-Cárdenas, O. F. Aguilar-Meza, G. May-Mora, and M. A. Reyes-Hernández for their technical assistance.

References Cited

1.

F. Agudelo-Silva 1986. Naturally occurring pathogens of Spodoptera frugiperda (Lepidoptera: Noctuidae) larvae collected in Venezuela. Florida Entomol. 69:768–769. Google Scholar

2.

L. Alcocer-Gomez and M. Mendez-Villa . 1965. Estudios preliminares sobre parasitismo en larvas de Laphigma frugiperda Smith y Abbot, por un nematodo de la familia mermitidae. Fitófilo 48:5–20. Google Scholar

3.

M. E. Barbercheck 1993. Tritrophic level effects on entomopathogenic nematodes. Environ. Entomol. 22:1166–1171. Google Scholar

4.

R. A. Bedding and R. A. Akhurst . 1975. A simple technique for the detection of insect parasitic rhabditid nematodes in soil. Nematologica 21:109–110. Google Scholar

5.

J. M. Bergman and W. M. Tingey . 1979. Aspects of interactions between plant genotypes and biological controls. Bull. Entomol. Soc. Am. 25:275–279. Google Scholar

6.

M. J. Bidochka, J. E. Kasperski, and G. A M. Wild . 1998. Occurrence of the entomopathogenic fungi Metarhizium anisopliae and Beauveria bassiana in soils from temperate and near-northern habitats. Can. J. Bot. 76:1198–1204. Google Scholar

7.

B. L K. Brady 1979. CMI description of pathogenic fungi and bacteria, Sets 61 and 62 (Nos. 601-620), Commonwealth Mycological Institute, England, UK. Google Scholar

8.

R. L. Burton and W. D. Perkins . 1989. Rearing the corn earworm and fall armyworm for maize resistance studies, pp. 37-45. In CIMMYT. 1989. Toward insect resistant maize for the third world: Proceedings of the International Symposium on methodologies for developing host plant resistance to maize insects. Mexico, D.F.: CIMMYT.  Google Scholar

9.

A. E. Bustillo-P. and F. J. Posada-F. . 1986. Pathogenicity of Nomuraea rileyi isolate to larvae of the maize borer Spodoptera frugiperda. Revista Colombiana de Entomología 12:5–15. Google Scholar

10.

T. Colborn 1995. Pesticides-how research has succeeded and failed to translate Science into Policy: Endocrinological effects on wildlife. Environ. Health Perspect. 103:81–86. Google Scholar

11.

P. Constant, L. Marchay, M. Fischer-Le Saux, S. Briand-Panoma, and H. Mauleon . 1998. Natural occurrence of entomopathogenic nematodes (Rhabditida: Steinernematidae and Heterorhabditidae) in Guadelopupe islands. Fund. Appl. Nematol. 21:667–672. Google Scholar

12.

B. A. Croft and A. W. Brown . 1975. Responses of arthropod natural enemies to insecticides. Annu. Rev. Entomol. 20:285–335. Google Scholar

13.

A. S. Crowe and W. G. Booty . 1995. A multi-level assessment methodology for determining the potential for groundwater contamination by pesticides. Environ. Monitor. Assess. 35:239–261. Google Scholar

14.

D. Chandler, D. Hay, and A. P. Reid . 1997. Sampling and occurrence of entomopathogenic fungi and nematodes in UK soils. Applied Soil Ecol. 5:133–141. Google Scholar

15.

J. Fargues and D. Rodriguez-Rueda . 1980. Sensibilité des larves de Spodoptera littoralis (Lepidoptera: Noctuidae) aux hyphomycètesentomopathogènes Nomuraea rileyi et Paecilomyces fumosoroseus. Entomophaga 25:43–54. Google Scholar

16.

J. R. Fuxa 1982. Prevalence of viral infection in populations of fall armyworm, Spodoptera frugiperda, in Southeastern Louisiana. Environ. Entomol. 11:239–242. Google Scholar

17.

J. R. Fuxa, A. R. Richter, and F. Agudelo-Silva . 1988. Effect of host age and nematode strain on susceptibility of Spodoptera frugiperda to Steinernema feltiae. J. Nematol. 20:91–95. Google Scholar

18.

W. A. Gardner and J. R. Fuxa . 1980. Pathogens for the suppression of the fall armyworm. Florida Entomol. 63:439–447. Google Scholar

19.

C. T. Griffin, R. Chaerani, D. Fallon, A. P. Reid, and M. J. Downes . 2000. Occurrence and distribution of the entomopathogenic nematodes Steinernema spp., and Heterorhaditis indica in Indonesia. J. Helminthol. 74:143–150. Google Scholar

20.

M. E M. Habib and P. N. Patel . 1990. Patogenicidade de Nomuraea rileyi (Farlow) Samson em larvas de Spodoptera frugiperda (J. E. Smith, 1797), praga de milho. Revista de Agricultura Piracicaba 65:83–90. Google Scholar

21.

J. J. Hamm 1980. Epizootics of Entomophthora aulicae in lepidopterous pests of sorghum. J. Invertebr. Pathol. 36:60–63. Google Scholar

22.

J. J. Hamm 1984. Invertebrate pathology and biological control. J. Georgia Entomol. Soc. 19:6–13. Google Scholar

23.

J. J. Hamm and B. R. Wiseman . 1986. Plant resistance and nuclear polyhedrosis virus for suppression of the fall armyworm (Lepidoptera: Noctuidae). Florida Entomol. 69:541–549. Google Scholar

24.

J. J. Hamm, S. D. Pair, and O. G. Marti . 1986. Incidence of host range of a new ascovirus isolated from fall armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae). Florida Entomol. 69:524–531. Google Scholar

25.

A. J. Hruska and F. Gould . 1997. Fall armyworm (Lepidoptera: Noctuidae)and Diatraea lineolata (Lepidoptera: Pyralidae): Impact of larval population level and temporal occurrence on maize yield in Nicaragua. J. Econ. Entomol. 90:611–622. Google Scholar

26.

R. E. Lecuona and A. A. Lanteri . 1999. Control microbiano con hongos entomopatógenos en la Argentina. Revista de la Sociedad Entomológica Argentina 58:301–306. Google Scholar

27.

R. Lezama-Gutierrez, R. Alatorre-Rosas, L. F. Bojalil-Jaber, J. Molina-Ochoa, M. Arenas-Vargas, M. Gonzalez-Ramirez, and O. Rebolledo-Dominguez . 1996. Virulence of five entomopathogenic fungi (Hyphomycetes) against Spodoptera frugiperda (Lepidoptera: Noctuidae) eggs and neonate larvae. Vedalia 3:35–39. Google Scholar

28.

R. Lezama-Gutierrez, J. J. Hamm, J. Molina-Ochoa, M. Lopez-Edwards, A. Pescador-Rubio, M. Gonzalez-Ramirez, and E. Styer . 2001. Occurrence of entomopathogens of Spodoptera frugiperda (Lepidoptera: Noctuidae) in the mexican states of Michoacan, Colima, Jalisco and Tamaulipas. Florida Entomol. 84:23–30. Google Scholar

29.

R. T. Mietkiewski, J. K. Pell, and S. J. Clark . 1997. Influence of pesticide use on the natural occurrence of entomopathogenic fungi in arable soils in the UK, field and laboratory comparisons. Biocontrol Sci. Technol. 7:565–575. Google Scholar

30.

R. Mietkiewski, M. Dziegielewska, and K. Janowicz . 1998. Entomopathogenic fungi isolated in the vicinity of Szczecin. Acta Mycologica 33:123–130. Google Scholar

31.

J. Molina-Ochoa, J. J. Hamm, R. Lezama-Gutierrez, L. F. Bojalil-Jaber, M. Arenas-Vargas, and M. Gonzalez-Ramirez . 1996. Virulence of six entomopathogenic nematodes (Steinernematidae and Heterorhabditidae) on immature stages of Spodoptera frugiperda (Lepidoptera: Noctuidae). Vedalia 3:25–29. Google Scholar

32.

J. Molina-Ochoa, B. R. Wiseman, R. Lezama-Gutierrez, J. J. Hamm, O. Rebolledo-Dominguez, M. Gonzalez-Ramirez, and M. Arenas-Vargas . 1997. Impact of resistant "Zapalote Chico" corn silks on Spodoptera frugiperda (Lepidoptera: Noctuidae) growth and development. Vedalia 4:31–34. Google Scholar

33.

J. Molina-Ochoa, R. Lezama-Gutierrez, J. J. Hamm, B. R. Wiseman, and M. Lopez-Edwards . 1999. Integrated control of fall armyworm (Lepidoptera: Noctuidae) using resistant plants and entomopathogenic nematodes (Rhabditida: Steinernematidae). Florida Entomol. 82:263–271. Google Scholar

34.

J. Molina-Ochoa, J. J. Hamm, R. Lezama-Gutierrez, M. Lopez-Edwards, M. Gonzalez-Ramirez, and A. Pescador-Rubio . 2001. A survey of fall armyworm (Lepidoptera: Noctuidae) parasitoids in the Mexican states of Michoacan, Colima, Jalisco, and Tamaulipas. Florida Entomol. 84:31–36. Google Scholar

35.

A. Pantoja, C. M. Smith, and J. F. Robinson . 1985. Natural control agents affecting Spodoptera frugiperda (Lepidoptera: Noctuidae) infesting rice in Puerto Rico. Florida Entomol. 68:488–490. Google Scholar

36.

A. Pantoja and J. R. Fuxa . 1992. Prevalence of biotic control agents in the fall armyworm Spodoptera frugiperda (J. E. Smith) (Lepidoptera: Noctuidae). Folia. Entomol. Mex. 84:79–84. Google Scholar

37.

P. N. Patel and M. E M. Habib . 1988. Protozoosis caused by Vairimorpha necatrix microsporidia Nosematidae in larvae of Spodoptera frugiperda Lepidoptera Noctuidae. Rev. Bras. Zool. 5:593–598. Google Scholar

38.

A. R. Richter and J. R. Fuxa . 1990. Effect of Steinernema feltiae on Spodoptera frugiperda and Heliothis zea (Lepidoptera: Noctuidae) in corn. J. Econ. Entomol. 83:1286–1291. Google Scholar

39.

J. S. Rosa, E. Bonifaassi, J. Aamarl, L. A. Lacey, N. Simoes, and C. Laumond . 2000. Natural occurrence of entomopathogenic nematodes (Rhabditida: Steinernema, Heterorhabditis) in the Azores. J. Nematol. 32:215–222. Google Scholar

40.

R. A. Samson, H. C. Evans, and J. P. Latgé . 1988. Atlas of entomopathogenic fungi. 187 pp. Springer-Verlag, Berlin, Germany. Google Scholar

41.

R. D. Schwehr and W. A. Gardner . 1982. Disease incidence in fall armyworm and corn earworm populations attacking grain sorghum. J. Georgia Entomol. Soc. 17:38–46. Google Scholar

42.

D. R. Sosa-Gomez and F. Moscardi . 1994. Effect of till and no-till soybean cultivation on dynamics of entomopathogenic fungi in the soil. Florida Entomol. 77:284–287. Google Scholar

43.

A. N. Sparks 1986. Fall armyworm (Lepidoptera: Noctuidae) potential for area-wide management. Florida Entomol. 69:603–614. Google Scholar

44.

N. Tangchitsomkid, S. Sontirat, Nuchanart-Tangchitsomkid, and Suebsak-Sontirat . 1998. Occurrence of entomopathogenic nematodes in Thailand. Kasetsart Journal Natural Sciences 32:347–354. Google Scholar

45.

E. Tarasco, C. De Bievre, B. Papierok, M. Poliseno, O. Triggiani, and C. De Bievre . 1997. Occurrence of entomopathogenic fungi in soils in Southern Italy. Entomologica 31:157–166. Google Scholar

46.

F. H. Valicente 1989. Levantamento dos inimigos naturais de Spodoptera frugiperda (J. E. Smith, 1797) (Lepidoptera: Noctuidae) em diferentes regioes de Minas Gerais. Annais da Sociedade Entomologica do Brasil 18:119–130. Google Scholar

47.

A. Van Huis 1981. Integrated pest management in the small farmer’s maize crop in Nicaragua. Med. Land. Wageningen 81:93–100. Google Scholar

48.

I. Vanninen 1996. Distribution and occurrence of four entomopathogenic fungi in Finland: Effect of geographical location, habitat type and soil type. Mycol. Res. 100:93–101. Google Scholar

49.

M. L. Vargas and G. Sanchez-G. . 1983. Natural control of some pests of the rice varieties IR-22 and CICA-6. Revista Colombiana de Entomología 9:50–54. Google Scholar

50.

M. L. Vera, L. Valverde, S. B. Popich, and Z. D. Ajmat-De Toledo . 1995. Preliminary evaluation of natural enemies of Spodoptera frugiperda (J. E. Smith) (Lepidoptera: Noctuidae) in Tucuman, Argentina. Acta Entomologica Chilena 19:135–141. Google Scholar

51.

G. S. Wheeler, T. R. Ashley, and K. L. Andrews . 1989. Larval parasitoids and pathogens of the armyworm in Honduran maize. Entomophaga:34:331–340. Google Scholar

52.

B. R. Wiseman and J. J. Hamm . 1993. Nuclear polyhedrosis virus and resistant corn silks enhance mortality of corn earworm (Lepidoptera: Noctuidae) larvae. Biological Control 3:337–342. Google Scholar

53.

J. L. Woodring and H. K. Kaya . 1988. Steinernematid and Heterorhabditid nematodes: A handbook of techniques. Southern Cooperative Series Bulletin 331. 30 pp. Arkansas Agricultural Experiment Station, Fayetteville. Google Scholar

Appendices

Table 1.

Geographic location, date, altitiude, crop (*), sample size (n), and total percent FAW larvae infected by entomopathogens and parasitic nematodes in six Mexican states (**) during 2000.

i0015-4040-86-3-244-t101.gif

Table 1.

(Continued) Geographic location, date, altitiude, crop (*), sample size (n), and total percent FAW larvae infected by entomopathogens and parasitic nematodes in six Mexican states (**) during 2000.

i0015-4040-86-3-244-t102.gif

Table 1.

(Continued) Geographic location, date, altitiude, crop (*), sample size (n), and total percent FAW larvae infected by entomopathogens and parasitic nematodes in six Mexican states (**) during 2000.

i0015-4040-86-3-244-t103.gif

Table 2.

Percentage of FAW larvae infected by entomopathogens and mermithids at each location.

i0015-4040-86-3-244-t201.gif

Table 2.

(Continued) Percentage of FAW larvae infected by entomopathogens and mermithids at each location.

i0015-4040-86-3-244-t202.gif

Table 3.

Entomopathogenic fungi (Hyphomycetes) and nematodes (Rhabditida: Steinernematidae and Heterorhabditidae) recovered from soil samples in different Mexican locations.

i0015-4040-86-3-244-t03.gif
Jaime Molina-Ochoa, Roberto Lezama-Gutierrez, Martin Gonzalez-Ramirez, Marilu Lopez-Edwards, Manuel A. Rodriguez-Vega, and Francisco Arceo-Palacios "PATHOGENS AND PARASITIC NEMATODES ASSOCIATED WITH POPULATIONS OF FALL ARMYWORM (LEPIDOPTERA: NOCTUIDAE) LARVAE IN MEXICO," Florida Entomologist 86(3), 244-253, (1 September 2003). https://doi.org/10.1653/0015-4040(2003)086[0244:PAPNAW]2.0.CO;2
Published: 1 September 2003
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