INTRODUCTION
The sexual communication system of a many of moth species is mediated by pheromones and may vary geographically among populations (Toth et al., 1992; Gemeno et al., 2000; Groot et al., 2009). This variation includes qualitative or quantitative changes of sexual pheromone components and/or male responses to them (Phelan, 1992; Baker, 2002; Smadja & Butlin, 2009). From a practical point of view, the geographical variation in sexual communication of moths may be important for the management of agricultural pests, by either monitoring or control (i.e., mass trapping, attraction-annihilation, or mating disruption) using synthetic pheromones (Cardé & Minks, 1995; El-Sayed et al., 2009; Witzgall et al., 2010). For instance, a monitoring program could be less successful if it uses pheromone lures formulated from populations distributed in regions different from the target population.
-
Toth et al., 1992
Attraction of male turnip moths Agrotis segetum (Lepidoptera:
Noctuidae) to sex pheromone components and their mixtures at 11 sites in
Europe, Asia, and Africa
Journal of Chemical Ecology, 1992
-
Gemeno et al., 2000
Pheromone blend variation and cross-attraction among populations
of the black cutworm moth (Lepidoptera: Noctuidae)
Annals of the Entomological Society of America, 2000
-
Groot et al., 2009
Geographic and temporal variation in moth chemical
communication
Evolution: International Journal of Organic Evolution, 2009
-
Phelan, 1992
Evolution of sex pheromones and the role of asymmetric
tracking
Insect Chemical Ecology: An Evolutionary Approach, 1992
-
Baker, 2002
Mechanism for saltational shifts in pheromone communication
systems
Proceedings of the National Academy of Sciences USA, 2002
-
Smadja & Butlin, 2009
On the scent of speciation: the chemosensory system and its role
in premating isolation
Heredity, 2009
-
Cardé & Minks, 1995
Control of moth pests by mating disruption: successes and
constraints
Annual Review of Entomology, 1995
-
El-Sayed et al., 2009
Potential of “lure and kill” in long-term pest management and
eradication of invasive species
Journal of Economic Entomology, 2009
-
Witzgall et al., 2010
Sex pheromones and their impact on pest
management
Journal of Chemical Ecology, 2010
The fall armyworm (FAW), Spodoptera frugiperda (J. E. Smith), is the most important insect pest of corn crops in Mexico (Blanco et al., 2014), but it is also widely distributed from north of the USA to north of Argentina (Prowell et al., 2004; Hardke et al., 2011; Pashley, 1986). However, recently, FAW has become a harmful, invasive pest of corn in sub-Saharan Africa (Goergen et al., 2016; Stokstad, 2017) and Asia (Wu et al., 2019; Padhee & Prasanna, 2019).
-
Blanco et al., 2014
Maize pests in Mexico and challenges for the adoption of
integrated pest management programs
Journal of Integrated Pest Management, 2014
-
Prowell et al., 2004
Multilocus genetic analysis of host use, introgression, and
speciation in host strains of fall armyworm (Lepidoptera:
Noctuidae)
Annals of the Entomological Society of America, 2004
-
Hardke et al., 2011
Damage and survivorship of fall armyworm (Lepidoptera: Noctuidae)
on transgenic field corn expressing Bacillus thuringiensis Cry
proteins
Crop Protection, 2011
-
Pashley, 1986
Host-associated genetic differentiation in fall armyworm
(Lepidoptera: Noctuidae): a sibling species complex?
Annals of the Entomological Society of America, 1986
-
Goergen et al., 2016
First report of outbreaks of the fall armyworm Spodoptera
frugiperda (JE Smith) (Lepidoptera, Noctuidae), a new alien invasive pest in
West and Central Africa
PloS One, 2016
-
Stokstad, 2017
New crop pest takes Africa at lightning speed
Science, 2017
-
Wu et al., 2019
Estimation of the potential infestation area of newly-invaded
fall armyworm Spodoptera frugiperda in the yangtze river valley of
China
Insects, 2019
-
Padhee & Prasanna, 2019
The emerging threat of fall armyworm in India
Indian Farming, 2019
Spodoptera frugiperda females expose the last abdominal segments for releasing their sex pheromone components into the environment during calling behavior (Cruz-Esteban et al., 2017). The effluvia and gland pheromone extracts from calling FAW females contain several acetates, including (Z)-9-tetradecenyl acetate (Z9-14:OAc) as a major component, (Z)-7-dodecenyl acetate (Z7-12:OAc), (Z)-11-hexadecenyl acetate (Z11-16:OAc), (Z)-9-dodecenyl acetate (Z9-12:OAc), and (E)-7-dodecenyl acetate (E7-12:OAc) (Mitchell et al., 1985; Tumlinson et al., 1986; Descoins et al., 1988; Groot et al., 2008; Lima & McNeil, 2009; Unbehend et al., 2013; Batista-Pereira et al., 2006). The latter compound has only been reported being produced by Brazilian FAW populations (Batista-Pereira et al., 2006).
-
Cruz-Esteban et al., 2017
Calling behavior, copulation time, and reproductive compatibility
of corn-strain fall armyworm (Lepidoptera: Noctuidae) from populations in
Mexico
Environmental Entomology, 2017
-
Mitchell et al., 1985
Field evaluation of commercial pheromone formulations and traps
using a more effective sex pheromone blend for the fall armyworm
(Lepidoptera: Noctuidae)
Journal of Economic Entomology, 1985
-
Tumlinson et al., 1986
Sex pheromone of fall armyworm, Spodoptera frugiperda (JE
Smith)
Journal of Chemical Ecology, 1986
-
Descoins et al., 1988
Monitoring of crop pests by sexual trapping of males in
Guadeloupe and Guyana
Agriculture, Ecosystems & Environment, 1988
-
Groot et al., 2008
Host strain specific sex pheromone variation in Spodoptera
frugiperda
Frontiers in Zoology, 2008
-
Lima & McNeil, 2009
Female sex pheromones in the host races and hybrids of the fall
armyworm, Spodoptera frugiperda (Lepidoptera: Noctuidae)
Chemoecology, 2009
-
Unbehend et al., 2013
Pheromonal divergence between two strains of Spodoptera
frugiperda
Journal of Chemical Ecology, 2013
-
Batista-Pereira et al., 2006
Isolation, identification, synthesis, and field evaluation of the
sex pheromone of the Brazilian population of Spodoptera
frugiperda
Journal of Chemical Ecology, 2006
-
Batista-Pereira et al., 2006
Isolation, identification, synthesis, and field evaluation of the
sex pheromone of the Brazilian population of Spodoptera
frugiperda
Journal of Chemical Ecology, 2006
Commercial FAW sex pheromone lures formulated from USA populations are used for monitoring this agricultural pest in several countries. However, the capture of FAW males by traps baited with these commercial lures are erratic when these were evaluated in Mexico, Central America and South America (Andrade et al., 2000; Malo et al., 2001; Batista-Pereira et al., 2006), suggesting that pheromonal communication of this moth species may vary geographically. Generally, the commercial lures of FAW are formulated with three pheromone components: Z9-14:OAc, Z11-16:OAc, and Z7-12:OAc (Malo et al., 2001; Bratovich et al., 2019). In Mexico, FAW females collected from corn consistently emitted Z9-14: OAc (65-90%), Z11-16: OAc (4-34%), and Z7-12: OAc (traces-5%) (Cruz-Esteban et al., 2018).
-
Andrade et al., 2000
Optimization of a pheromone lure for Spodoptera frugiperda
(Smith) in Central America
Journal of the Brazilian Chemical Society, 2000
-
Malo et al., 2001
Evaluation of commercial pheromone lures and traps for monitoring
male fall armyworm (Lepidoptera: Noctuidae) in the coastal region of
Chiapas, Mexico
Florida Entomologist, 2001
-
Batista-Pereira et al., 2006
Isolation, identification, synthesis, and field evaluation of the
sex pheromone of the Brazilian population of Spodoptera
frugiperda
Journal of Chemical Ecology, 2006
-
Malo et al., 2001
Evaluation of commercial pheromone lures and traps for monitoring
male fall armyworm (Lepidoptera: Noctuidae) in the coastal region of
Chiapas, Mexico
Florida Entomologist, 2001
-
Bratovich et al., 2019
Evaluation of sex pheromone formulations to attract Spodoptera
frugiperda (Lepidoptera: Noctuidae) adult males in Argentina
Revista de la Sociedad Entomológica Argentina, 2019
-
Cruz-Esteban et al., 2018
Geographic variation in pheromone component ratio and antennal
responses, but not in attraction, to sex pheromones among fall armyworm
populations infesting corn in Mexico
Journal of Pest Science, 2018
In this work, we investigated whether all three components emitted by FAW females from Mexican populations are crucial for attracting conspecific males in field conditions. The objective of this work was the optimization of a sex pheromone lure that would be useful for monitoring S. frugiperda in corn crops in Mexico.
MATERIALS AND METHODS
Chemicals. Synthetic Z7-12:OAc, Z9-14:OAc and Z11-16:OAc were purchased from commercial sources (Sigma-Aldrich, Toluca, Mexico). The purity of synthetic compounds (<97%) was determined with a Shimadzu GC-2010 plus gas chromatograph (Tokyo, Japan) equipped with a flame ionization detector. We prepared standard solutions of the compounds in (HPLC)-grade hexane (Sigma-Aldrich, Toluca, Mexico).
Field tests. In the first experiment, we evaluated the attractiveness of single compounds or the binary and tertiary blends of synthetic pheromone compounds formulated according to the relative proportion of each compound as released by FAW females from Tapachula, Chiapas (Cruz-Esteban et al., 2018). The compound (Z7-12:OAc) that was found at trace levels was assigned to 1% of the blend. The experiment was performed in the Ejido Joaquín Miguel Gutiérrez (14° 44' N, 92° 19' W), municipality of Tapachula, Chiapas, Mexico, in March 2017. This experiment was deployed in a fully randomized block design with four replicates per treatment. In each block, nine yellow plastic jug traps (Malo et al., 2018) were used for one of each treatment (see below). The blocks were arranged in parallel lines separated ca. 50 m apart in a corn crop (approximately 8 ha). Rubber septa lures containing 400 µg of each synthetic compound (Z9-14:OAc, Z7-12:OAc or Z11-16:OAc) or the binary and tertiary blends were placed in the traps. A virgin female of four-five day old, reared in the laboratory, was used as a positive control, and a non-baited trap was used as a negative control. The traps with the lures were hung at a height of 1.5 m above the ground on wooden stakes placed 50 m apart from each another.
-
Cruz-Esteban et al., 2018
Geographic variation in pheromone component ratio and antennal
responses, but not in attraction, to sex pheromones among fall armyworm
populations infesting corn in Mexico
Journal of Pest Science, 2018
-
Malo et al., 2018
A home-made trap baited with sex pheromone for monitoring
Spodoptera frugiperda males (Lepidoptera: Noctuidae) in corn crops in
Mexico
Journal of Economic Entomology, 2018
In the second experiment, we tested the effect of the proportion of the most attractive blend obtained in the first experiment. This experiment was performed in the Ejido Joaquín Miguel Gutiérrez in June 2017. The experiment was deployed in a fully randomized block design. Yellow plastic jug traps were placed and distributed as in the first experiment. Lures consisted of rubber septa loaded with 400 µg of Z7-12:OAc + Z9-14:OAc at 99:1, 1:99, 50:50, 89:11, or 11:89 proportion.
In the third experiment, we evaluated the effect of three proportions (1:99, 1.5:98.5, and 2:98) of the binary blend Z7-12:OAc + Z9-14:OAc for catching FAW males. Three trials of this experiment were performed, one in the Ejido Joaquín Miguel Gutiérrez, another in San Nicolás Lagartero (14° 49' N, 92° 15' W), Tapachula, Chiapas, and Ciudad Guzmán (19° 42' N, 103° 28' W), Jalisco. The distance between the Ejido Joaquín Miguel Gutiérrez and San Nicolás Lagartero was greater than 10 km. The first two trials were performed during August-September 2017. The distribution of the yellow plastic jug traps was like the first experiment.
In the fourth experiment, we tested the effect of the dose of the binary blend of Z7-12:OAc + Z9-14:OAc on the capture of FAW males. The experiment was performed in the Ejido Joaquín Miguel Gutiérrez in October-November 2017. The experiment was deployed in a fully randomized block design. The distribution of the yellow plastic jug traps was like the first experiment. Rubber septa were loaded with 200, 400, 600, or 1600 µg of Z7-12:OAc + Z9-14:OAc (99:1).
In all experiments, the traps were checked every 3 days. On each observation date, traps were emptied, and the number of males caught was recorded. Treatments were rotated within each block, and all experiment lures were changed every 15 days and virgin females were exchanged daily for another of the same age.
Data analysis. Data were analyzed with statistical
software R version 3.6.1 (R Development Core Team,
2019). The number of moths captured/trap/night was analyzed by repeated
measures analysis of variance (ANOVA). Prior to analysis, we checked that data meet
the ANOVA´s assumptions, otherwise they were transformed according to the Box-Cox
method. Treatment means were compared with a Tukey test (α = 0.05).
-
R Development Core Team,
2019
R: A language and environment for statistical computing, 2019
RESULTS
In the first experiment, we found that the treatments affected the captures of FAW males (F = 17.6; df = 8, 135; P < 0.001). Traps baited with the binary blend of Z9-14:OAc + Z7-12:OAc caught significantly more FAW males than traps baited with other treatments (Fig. 1). Traps baited with Z7-12:OAc caught a similar number of males as traps baited with females. There were no differences in the number of FAW males captured by traps baited with Z9-14:OAc alone, Z11-16:OAc alone, Z7-12:OAc + Z11-16:OAc, Z9-14:OAc + Z11-16:OAc, Z7-12:OAc + Z9-14:OAc + Z11-16:OAc, and non-baited traps (Fig. 1).
Figure 1
Mean number (± S. E.) of males caught by traps baited with single compounds, binary, and tertiary blend in corn cultivations. The binary and tertiary blends were prepared according was found in the effluvia of females from Tapachula, Chiapas. The numbers related to each compound are the percentages used to prepare the blend, and the different letters above column indicate significant differences among treatments (α = 0.05).
In the second experiment, our results showed that the proportion of the Z9-14: OAc+Z7-12:OAc blend affected the capture of FAW males (F = 16.6; df = 4, 95; P < 0.0001). Traps baited with the proportion 99:1 of this binary blend captured more males in comparison to the other proportions tested (Fig. 2).
Figure 2
Mean number (± S. E.) of males caught by traps baited with blends of different proportion of the synthetic components (Z7-12:OAc + Z9-14:OAc) tested in corn cultivations. The numbers related to each compound are the percentages used to prepare the blend, and different letters above column indicate significant differences among treatments (α = 0.05).
In the third experiment, we found that there was no effect of the three proportions of the binary blend Z9-14:OAc + Z7-12:OAc tested on the FAW male captures in the Ejido Joaquín Miguel Gutiérrez (F = 1.8; df = 2, 126; P = 0.71) and Ejido San Nicolás Lagartero (F = 1.52; df = 2, 117; P = 0.22), Tapachula, Chiapas (Fig. 3A, 3B), but there was a significant effect at Ciudad Guzman (F = 11.64; df = 2,105; P < 0.0001), Jalisco (Fig. 3C). In the last location (Jalisco), traps baited with the proportion 99:1 (Z9-14:OAc and Z7-12:OAc, respectively) captured more FAW males than traps baited with the proportions of 98.5:1.5 and 98:2 (Fig. 3C). In the two experiments that were carried out in Tapachula, Chiapas, the proportion of 99:1 (Z9-14:OAc and Z7-12:OAc, respectively) attracted numerically the largest number of males (Fig. 3A, 3B).
Figure 3
Mean number (± S. E.) of males caught by traps baited with the binary blend (Z7-12:OAc + Z9-14:OAc) in different proportion in corn cultivations. (A) Joaquín Miguel Gutiérrez, Tapachula Chiapas, Mexico. (B) San Nicolás Lagartero, Tapachula Chiapas, Mexico. (C) Ciudad Guzmán, Jalisco, Mexico. The numbers related to each compound are the percentages used to prepare the blend, and the letters above column indicate significant differences among treatments (α = 0.05).
In the fourth experiment, our results showed that the dose of the blend constituted by the Z9-14: OAc + Z7-12:OAc blend affected the capture of FAW males (F = 14.47; df = 4, 5; P < 0.001). Traps baited with 600 µg of Z9-14: OAc + Z7-12:OAc captured more males than traps baited with 200 µg of this blend or non-baited traps (Fig. 4). The captures of traps baited with 600 µg of the blend were not different than those baited with 400 and 1600 µg of the blend. There were no significant differences in the captures of traps baited with 200 µg of the blend and those traps baited with 400 and 1600 µg of the blend (Fig. 4).
Figure 4
Mean number (( S. E.) of males caught by traps baited with different doses (µg) of the
binary blend of Z9-14:OAc (99%) +
Z7-12:OAc (1%) tested in the corn cultivations. The
numbers related to each compound are the percentages used to prepare the
blend, and different letters above column indicate significant
differences among treatments (α = 0.05).
DISCUSSION
In this study, we optimized a synthetic sexual pheromone for monitoring S. frugiperda males in Mexico. Our results demonstrated that the binary blend of Z9-14:OAc + Z7-12:OAc captured more males. Previously, we found that Z11-16:OAc elicited lower antennal responses in comparison to those evoked by Z9-14:OAc and Z7-12:OAc (Cruz-Esteban et al., 2018). Thus, the male antennal responses matched with the attraction of FAW males to both compounds. Our results also confirm that both acetates are critical components of the sex pheromones of FAW, as reported previously for other studies performed in several regions of the North American continent (Tumlinson et al., 1986; Andrade et al., 2000; Fleischer et al., 2005; Unbehend et al., 2014), but not in Brazil. In the latter country, in addition to Z7-12:OAc and Z9-14:OAc, E12:OAc is a third active component in the sex pheromone of the Brazilian populations of S. frugiperda (Batista-Pereira et al., 2006).
-
Cruz-Esteban et al., 2018
Geographic variation in pheromone component ratio and antennal
responses, but not in attraction, to sex pheromones among fall armyworm
populations infesting corn in Mexico
Journal of Pest Science, 2018
-
Tumlinson et al., 1986
Sex pheromone of fall armyworm, Spodoptera frugiperda (JE
Smith)
Journal of Chemical Ecology, 1986
-
Andrade et al., 2000
Optimization of a pheromone lure for Spodoptera frugiperda
(Smith) in Central America
Journal of the Brazilian Chemical Society, 2000
-
Fleischer et al., 2005
Spodoptera frugiperda pheromone lures to avoid nontarget captures
of Leucania phragmatidicola
Journal of Economic Entomology, 2005
-
Unbehend et al., 2014
Geographic variation in sexual attraction of Spodoptera
frugiperda corn-and rice-strain males to pheromone lures
PloS One, 2014
-
Batista-Pereira et al., 2006
Isolation, identification, synthesis, and field evaluation of the
sex pheromone of the Brazilian population of Spodoptera
frugiperda
Journal of Chemical Ecology, 2006
We found that a change in the proportions of Z7-12:OAc and Z14:OAc did not affect the capture of FAW males in Chiapas, but it did in Jalisco. This result could suggest that there is a geographical variation in the sexual communication in the Mexican populations of S. frugiperda. However, in a previous study, we found that while the proportion of pheromone components emitted by females and the male antennal responses to the compounds varied among regions, males were not differentially caught by traps baited with different proportions of Z7-12:OAc, Z9-14:OAc and Z11-16:OAc (Cruz-Esteban et al., 2018). Thus, other factors such as habitat composition or population density of FAW may affect the capture of FAW males in Chiapas and Jalisco. For example, traps were placed in different corn varieties from different phenological states. Environmental factors were also different in the experimental sites. Thus, background odors could have influenced the response of the males to their pheromone. For instance, other studies have documented that capture of FAW males of the corn race differ in traps baited with the same pheromone blend placed in sorghum, corn, rice, sugarcane, turfgrass or vegetables located in North and South Florida, USA (Unbehend et al., 2013; Meagher & Nagoshi, 2013). Previously, we reported that host volatiles elicited antennal responses in both sexes of S. frugiperda (Malo et al., 2004). Further studies will be performed to investigate the role of host volatiles in the male response to sex pheromones.
-
Cruz-Esteban et al., 2018
Geographic variation in pheromone component ratio and antennal
responses, but not in attraction, to sex pheromones among fall armyworm
populations infesting corn in Mexico
Journal of Pest Science, 2018
-
Unbehend et al., 2013
Pheromonal divergence between two strains of Spodoptera
frugiperda
Journal of Chemical Ecology, 2013
-
Meagher & Nagoshi, 2013
Attraction of fall armyworm males (Lepidoptera: Noctuidae) to
host strain females
Environmental Entomology, 2013
-
Malo et al., 2004
Antennal sensilla and electrophysiological response of male and
female Spodoptera frugiperda (Lepidoptera: Noctuidae) to conspecific sex
pheromone and plant odors
Annals of the Entomological Society of America, 2004
At first glance, it seems that the addition of Z11-16:OAc to the binary blend of Z9-14:OAc + Z7-12:OAc interrupted the capture of FAW males. This result could also explain the erratic results of male capture by commercially available sex pheromones of S. frugiperda, which, generally, contain Z11-16:OAc (Malo et al., 2001; Bratovich et al., 2019). However, Z11-16:OAc did not affect the capture of FAW males when added to Z7-12:OAc and Z14:OAc in similar trials in Florida, USA, Brazil, and Argentina (Tumlinson et al., 1986; Batista-Pereira et al., 2006). A possibility to explain this contradiction is that we used a higher percentage of Z11-16:OAc in the tertiary blend compared to previous studies. However, Cruz-Esteban et al. (2018) found that a similar percentage of Z11-16:OAc in the tertiary blend did not affect the males caught in the same region that we performed the present study. Unfortunately, the binary blend of Z7-12:OAc and Z9-14:OAc was not included in the study of Cruz-Esteban et al. (2018). The compound Z11-16:OAc was found in the effluvia of calling females from 22 regions of Mexico (Cruz-Esteban et al., 2018). It will be necessary to perform further experiments to investigate if this compound has an ecological role in the sexual communication of S. frugiperda or if it is only an unavoidable byproduct of the pheromone biosynthetic pathway of this moth species (Groot et al., 2008).
-
Malo et al., 2001
Evaluation of commercial pheromone lures and traps for monitoring
male fall armyworm (Lepidoptera: Noctuidae) in the coastal region of
Chiapas, Mexico
Florida Entomologist, 2001
-
Bratovich et al., 2019
Evaluation of sex pheromone formulations to attract Spodoptera
frugiperda (Lepidoptera: Noctuidae) adult males in Argentina
Revista de la Sociedad Entomológica Argentina, 2019
-
Tumlinson et al., 1986
Sex pheromone of fall armyworm, Spodoptera frugiperda (JE
Smith)
Journal of Chemical Ecology, 1986
-
Batista-Pereira et al., 2006
Isolation, identification, synthesis, and field evaluation of the
sex pheromone of the Brazilian population of Spodoptera
frugiperda
Journal of Chemical Ecology, 2006
-
Cruz-Esteban et al. (2018)
Geographic variation in pheromone component ratio and antennal
responses, but not in attraction, to sex pheromones among fall armyworm
populations infesting corn in Mexico
Journal of Pest Science, 2018
-
Cruz-Esteban et al. (2018)
Geographic variation in pheromone component ratio and antennal
responses, but not in attraction, to sex pheromones among fall armyworm
populations infesting corn in Mexico
Journal of Pest Science, 2018
-
Cruz-Esteban et al., 2018
Geographic variation in pheromone component ratio and antennal
responses, but not in attraction, to sex pheromones among fall armyworm
populations infesting corn in Mexico
Journal of Pest Science, 2018
-
Groot et al., 2008
Host strain specific sex pheromone variation in Spodoptera
frugiperda
Frontiers in Zoology, 2008
Our results suggest that a dose of 400 or 600 (g can be used for monitoring S. frugiperda males. In contrast, other authors used 2000 (g of the sex pheromone blend (Tumlinson et al., 1986; Andrade et al., 2000). However, our results were similar to those reported by Unbehend et al. (2014), who found that a blend of 300 (g of Z9-14:OAc + 6 (g Z7-12:OAc was the most effective to capture males of S. frugiperda in corn fields in several countries in North and South America. In Mexico, only Z9-14:OAc and Z7-12:OAc are needed to capture S. frugiperda males in corn and sorghum fields, it differs to other regions where it needs the addition of Z11-16:OAc and Z9-12:OAc (Malo et al., 2001; Bratovich et al., 2019). Future studies will be necessary to test the commercial sex pheromones of S. frugiperda to find the most attractive for geographical region.
-
Tumlinson et al., 1986
Sex pheromone of fall armyworm, Spodoptera frugiperda (JE
Smith)
Journal of Chemical Ecology, 1986
-
Andrade et al., 2000
Optimization of a pheromone lure for Spodoptera frugiperda
(Smith) in Central America
Journal of the Brazilian Chemical Society, 2000
-
Unbehend et al. (2014)
Geographic variation in sexual attraction of Spodoptera
frugiperda corn-and rice-strain males to pheromone lures
PloS One, 2014
-
Malo et al., 2001
Evaluation of commercial pheromone lures and traps for monitoring
male fall armyworm (Lepidoptera: Noctuidae) in the coastal region of
Chiapas, Mexico
Florida Entomologist, 2001
-
Bratovich et al., 2019
Evaluation of sex pheromone formulations to attract Spodoptera
frugiperda (Lepidoptera: Noctuidae) adult males in Argentina
Revista de la Sociedad Entomológica Argentina, 2019
In summary, we found that traps baited with binary blends of pheromones Z9-14:OAc (99%) and Z7-12:OAc (1%) caught significantly more S. frugiperda males in corn crops compared to other binary blends, a tertiary blend of Z7-12:OAc, Z9-14:OAc, and Z11-16:OAC, and a natural pheromone (e.g., females). This result suggests that this blend may be useful for monitoring FAW males in Mexico. Future studies will be performed to test the binary blend of the sex pheromone using a mass trapping to control S. frugiperda in corn crops in Mexico.
Acknowledgements
We thank Armando Virgen Sanchez, Neby M. Méridia Torres, and Álvaro José Campuzano Granados for their support in field tests, and Ferosex S.A. de C.V. for the logistic support during the trial performed in Jalisco. SCE (CVU: 316166) acknowledges receipt of a doctoral scholarship from the Mexican National Council for Science and Technology (CONACyT).
LITERATURE CITED
Andrade, R., Rodriguez, C., Oehlschlager, A. C. (2000)
Optimization of a pheromone lure for
Spodoptera frugiperda
(Smith) in Central America.
Journal of the Brazilian Chemical
Society, 11 (6), 609-613.
http://dx.doi.org/10.1590/S0103-50532000000600009
Links
Baker, T. C. (2002) Mechanism for saltational shifts in
pheromone communication systems.
Proceedings of the National Academy of
Sciences USA, 99 (21), 13368-13370.
https://doi.org/10.1073/pnas.222539799
Links
Batista-Pereira, L. G., Stein, K., de Paula, A. F., Moreira,
J. A., Cruz, I., Figueiredo, M. L. C., Perri, J. Jr., Corrêa, A. G.
(2006) Isolation, identification, synthesis, and field evaluation of the sex
pheromone of the Brazilian population of
Spodoptera frugiperda.
Journal of Chemical Ecology, 32 (5), 1085.
https://doi.org/10.1007/s10886-006-9048-5
Links
Blanco, C. A., Pellegaud, J. G., Nava-Camberos, U.,
Lugo-Barrera, D., Vega-Aquino, P., Coello, J., Terán-Vargas, A. P.,
Vargas-Camplis, J. (2014) Maize pests in Mexico and challenges for
the adoption of integrated pest management programs.
Journal of
Integrated Pest Management, 5 (4), E1-E9.
https://doi.org/10.1603/IPM14006
Links
Bratovich, C., Saluso, A., Murua, M. G., Guerenstein, P.
G. (2019) Evaluation of sex pheromone formulations to attract
Spodoptera frugiperda (Lepidoptera: Noctuidae) adult males
in Argentina.
Revista de la Sociedad Entomológica Argentina, 78
(3), 7-14.
Links
Cardé, R. T., Minks, A. K. (1995) Control of moth pests
by mating disruption: successes and constraints.
Annual Review of
Entomology, 40 (1), 559-585.
https://doi.org/10.1146/annurev.en.40.010195.003015
Links
Cruz-Esteban, S., Rojas, J. C., Malo, E. A. (2017)
Calling behavior, copulation time, and reproductive compatibility of corn-strain
fall armyworm (Lepidoptera: Noctuidae) from populations in Mexico.
Environmental Entomology, 46 (4), 901-906.
https://doi.org/10.1093/ee/nvx120
Links
Cruz-Esteban, S., Rojas, J. C., Sánchez-Guillén, D.,
Cruz-López, L., Malo, E. A. (2018) Geographic variation in pheromone
component ratio and antennal responses, but not in attraction, to sex pheromones
among fall armyworm populations infesting corn in Mexico.
Journal of
Pest Science, 91 (3), 973-983.
https://doi.org/10.1007/s10340-018-0967-z
Links
Descoins, C., Silvain, J. F., Lalanne-Cassou, B., Cheron,
H. (1988) Monitoring of crop pests by sexual trapping of males in
Guadeloupe and Guyana.
Agriculture, Ecosystems &
Environment, 21 (1-2), 53-56.
https://doi.org/10.1016/0167-8809(88)90139-9
Links
El-Sayed, A. M., Suckling, D. M., Byers, J. A., Jang, E. B.,
Wearing, C. H. (2009) Potential of “lure and kill” in long-term pest
management and eradication of invasive species.
Journal of Economic
Entomology, 102 (3), 815-835.
https://doi.org/10.1603/029.102.0301
Links
Fleischer, S. J., Harding, C. L., Blom, P. E., White, J.,
Grehan, J. (2005)
Spodoptera frugiperda pheromone
lures to avoid nontarget captures of
Leucania phragmatidicola.
Journal of Economic Entomology, 98 (1), 66-71.
https://doi.org/10.1093/jee/98.1.66
Links
Gemeno, C., Lutfallah, A. F., Haynes, K. F. (2000)
Pheromone blend variation and cross-attraction among populations of the black
cutworm moth (Lepidoptera: Noctuidae).
Annals of the Entomological
Society of America, 93 (6), 1322-1328.
https://doi.org/10.1603/0013-8746(2000)093[1322:PBVACA]2.0.CO;2
Links
Goergen, G., Kumar, P. L., Sankung, S. B., Togola, A., Tamò,
M. (2016) First report of outbreaks of the fall armyworm
Spodoptera frugiperda (JE Smith) (Lepidoptera, Noctuidae),
a new alien invasive pest in West and Central Africa.
PloS One,
11 (10), e0165632. https://doi.org/10.1371/journal.pone.0165632
Links
Groot, A. T., Marr, M., Schöfl, G., Lorenz, S., Svatos, A.,
Heckel, D. G. (2008) Host strain specific sex pheromone variation in
Spodoptera frugiperda.
Frontiers in
Zoology, 5 (1), 20. https://doi.org/10.1186/1742-9994-5-20
Links
Groot, A. T., Inglis, O., Bowdridge, S., Santangelo, R. G.,
Blanco, C., López, Jr., Terán-Vargas, A., Fred, G., Schal, C. (2009)
Geographic and temporal variation in moth chemical communication.
Evolution: International Journal of Organic Evolution, 63
(8), 1987-2003. https://doi.org/10.1111/j.1558-5646.2009.00702.x
Links
Hardke, J. T., Leonard, B. R., Huang, F., Jackson, R.
E. (2011) Damage and survivorship of fall armyworm (Lepidoptera:
Noctuidae) on transgenic field corn expressing
Bacillus
thuringiensis Cry proteins.
Crop Protection, 30
(2), 168-172. https://doi.org/10.1016/j.cropro.2010.10.005
Links
Lima, E. R., McNeil, J. N. (2009) Female sex pheromones
in the host races and hybrids of the fall armyworm,
Spodoptera
frugiperda (Lepidoptera: Noctuidae).
Chemoecology,
19 (1), 29-36. https://doi.org/10.1007/s00049-009-0005-y
Links
Malo, E. A., Cruz-Lopez, L., Valle-Mora, J., Virgen, A.,
Sanchez, J. A., Rojas, J. C. (2001) Evaluation of commercial
pheromone lures and traps for monitoring male fall armyworm (Lepidoptera:
Noctuidae) in the coastal region of Chiapas, Mexico.
Florida
Entomologist, 84 (4), 659-664.
Links
Malo, E. A., Castrejón-Gómez, V. R., Cruz-López, L., Rojas, J.
C. (2004) Antennal sensilla and electrophysiological response of male
and female
Spodoptera frugiperda (Lepidoptera: Noctuidae) to
conspecific sex pheromone and plant odors.
Annals of the Entomological
Society of America , 97 (6), 1273-1284.
https://doi.org/10.1603/0013-8746(2004)097[1273:ASAERO]2.0.CO;2
Links
Malo, E. A., Cruz-Esteban, S., González, F. J., Rojas, J.
C. (2018) A home-made trap baited with sex pheromone for monitoring
Spodoptera frugiperda males (Lepidoptera: Noctuidae) in
corn crops in Mexico.
Journal of Economic Entomology , 111 (4),
1674-1681. https://doi.org/10.1093/jee/toy128
Links
Meagher, R. L., Nagoshi, R. N. (2013) Attraction of
fall armyworm males (Lepidoptera: Noctuidae) to host strain females.
Environmental Entomology , 42 (4), 751-757.
https://doi.org/10.1603/EN13007
Links
Mitchell, E. R., Tumlinson, J. H., McNeil, J. N. (1985)
Field evaluation of commercial pheromone formulations and traps using a more
effective sex pheromone blend for the fall armyworm (Lepidoptera: Noctuidae).
Journal of Economic Entomology , 78 (6), 1364-1369.
https://doi.org/10.1093/jee/78.6.1364
Links
Padhee, A. K., Prasanna, B. M. (2019) The emerging
threat of fall armyworm in India.
Indian Farming, 69 (1),
51-54.
Links
´Pashley, D. P. (1986) Host-associated genetic
differentiation in fall armyworm (Lepidoptera: Noctuidae): a sibling species
complex?
Annals of the Entomological Society of America , 79
(6), 898-904. https://doi.org/10.1093/aesa/79.6.898
Links
Phelan, P. L. (1992) Evolution of sex pheromones and
the role of asymmetric tracking.
Insect Chemical Ecology: An
Evolutionary Approach, 265-314. Kluwer,
Netherlands.
Links
Prowell, D. P., McMichael, M., Silvain, J. F. (2004)
Multilocus genetic analysis of host use, introgression, and speciation in host
strains of fall armyworm (Lepidoptera: Noctuidae).
Annals of the
Entomological Society of America , 97 (5), 1034-1044.
https://doi.org/10.1603/0013-8746(2004)097[1034:MGAOHU]2.0.CO;2
Links
R Development Core Team (2019) R: A language and
environment for statistical computing. R Foundation for Statistical Computing,
Vienna, Austria. Available online:
http://www.R-project.org/
Links
Smadja, C., Butlin, R. K. (2009) On the scent of
speciation: the chemosensory system and its role in premating isolation.
Heredity, 102 (1), 77-97.
https://doi.org/10.1038/hdy.2008.55
Links
Stokstad, E. (2017) New crop pest takes Africa at
lightning speed.
Science, 356 (6337), 473-474.
https://doi.org/10.1126/science.356.6337.473
Links
Toth, M., Löfstedt, C., Blair, B. W., Cabello, T., Farag, A.
I., Hansson, B. S., Kovalec, B. G., Maini, S., Nesterov, E. A., Pajor, I.,
Sazonov, A. P., Shamshev, I. V., Subchev, M., Szöcs, G. (1992)
Attraction of male turnip moths
Agrotis segetum (Lepidoptera:
Noctuidae) to sex pheromone components and their mixtures at 11 sites in Europe,
Asia, and Africa.
Journal of Chemical Ecology, 18 (8),
1337-1347. https://doi.org/10.1007/BF00994360
Links
Tumlinson, J. H., Mitchell, E. R., Teal, P. E. A., Heath, R.
R., Mengelkoch, L. J. (1986) Sex pheromone of fall armyworm,
Spodoptera frugiperda (JE Smith).
Journal of
Chemical Ecology, 12 (9), 1909- 1926.
https://doi.org/10.1007/BF01041855
Links
Unbehend, M., Hänniger, S., Meagher, R. L., Heckel, D. G.,
Groot, A. T. (2013) Pheromonal divergence between two strains of
Spodoptera frugiperda.
Journal of Chemical
Ecology, 39 (3), 364-376.
https://doi.org/10.1007/s10886-013-0263-6
Links
Unbehend, M., Hänniger, S., Vásquez, G. M., Juárez, M. L.,
Reisig, D., McNeil, J. N., Meager R. L., Jenkins, D. A., Heckel, D. G.,
Groot, A. T. (2014) Geographic variation in sexual attraction of
Spodoptera frugiperda corn-and rice-strain males to
pheromone lures.
PloS One , 9(2), e89255.
https://doi.org/10.1371/journal.pone.0089255
Links
Witzgall, P., Kirsch, P., Cork, A. (2010) Sex
pheromones and their impact on pest management.
Journal of Chemical
Ecology, 36 (1), 80-100.
https://doi.org/10.1007/s10886-009-9737-y
Links
Wu, Q. L., He, L. M., Shen, X. J., Jiang, Y. Y., Liu, J., Hu,
G., Wu, K. M. (2019) Estimation of the potential infestation area of
newly-invaded fall armyworm
Spodoptera frugiperda in the
yangtze river valley of China.
Insects, 10 (9), 298.
https://doi.org/10.3390/insects10090298
Links