Manipulation of fire ant density, Solenopsis spp., for short-term reduction of Diatraea saccharalis larval densities in Brazil

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Rearing of Pseudacteon spp (Dipt, Phoridae), parasitoids of fire ants (Solenopsis spp) (Hym, Formicidae)

After exposure of Solenopsis saevissima colonies maintained in plastic trays to phorid attack in the field, and subsequent transfer of colonies to covered plastic buckets, we confirmed that P. wasmanni and P. litoralis are indeed parasitoids of fire ant workers. The period from attack to emergence of phorid adults ranged from 35 to 46 days. Adult phorids were maintained live in glass vials with sugar water as a food source for 5 days. These results indicate that Pseudaceton can be reared for biological control release programs with minimal difficulty. Furthermore, parasitized workers could be easily transferred from South America to quarantine laboratories within the egg to adult emergence time period.

HOST-SPECIFICITY OF SEVERAL PSEUDACTEON (DIPTERA, PHORIDAE) PARASITES OF FIRE ANTS (HYMENOPTERA, FORMICIDAE) IN SOUTH-AMERICA

We tested the host specificity of several parasitic Pseudacteon scuttle flies in South America with 23 species of ants in 13 genera. None of these ant species attracted Pseudacteon parasites except Solenopsis saevissima (F. Smith) and to a lesser extent Solenopsis geminata (Fab.). This result is encouraging because it indicates that the Pseudacteon flies tested in this study would not pose an ecological danger to other ant genera if these flies were introduced into the United States as classical biological control agents of imported fire ants. This prediction of host specificity will, of course, need to be validated with potential hosts in the United States before these flies can be released.

SOLENOPSIS (HYMENOPTERA, FORMICIDAE) FIRE ANT REACTIONS TO ATTACKS OF PSEUDACTERON FLIES (DIPTERA, PHORIDAE) IN SOUTHEASTERN BRAZIL

We studied the responses of Solenopsis fire ants to Pseudacteon phorid fly attacks in southeastern Brazil. The presence of these phorid parasites triggered a suite of phorid-specific defense responses including reduced foraging, bait guarding, a curled defensive posture, and general colony immobility. The existence of these phorid-specific defenses indicates that Pseudacteon phorids exert substantial evolutionary pressure on South American fire ant populations.

FIRE ANT MOUND DENSITIES IN THE UNITED-STATES AND BRAZIL (HYMENOPTERA, FORMICIDAE)

To compare fire ant populations (Solenopsis) in North and South America, we surveyed 102 preselected roadside sites, half in the southeastern United States and half in the state of Mato Grosso do Sul, Brazil. Fire ants were considerably more abundant in the United States. They occurred at more sites (100 versus 70%), in higher densities (170 versus 30 mounds/ha), in larger mounds (27.0 versus 13.8 liters), and they constituted a larger fraction of the local ant community (97 versus 13% of occupied baits). These data are consistent with the hypothesis that North American populations of S. invicta have escaped natural biological control; however, cultural and climatic factors are also likely explanations.

Intercontinental Differences in the Abundance of Solenopsis Fire Ants (Hymenoptera: Formicidae): Escape from Natural Enemies?

The absence of natural enemies often allows exotic pests to reach densities that are much higher than normally occur in their native habitats. When Solenopsis fire ants were introduced into the United States, their numerous natural enemies were left behind in South America. To compare intercontinental fire ant densities, we selected 13 areas in South America and another 12 areas in North America. Sample areas were paired with weather stations and distributed across a broad range of climatic conditions. In each area, we measured fire ant densities at 5 preselected roadside sites that were at least 5 km apart. At each site, we also measured foraging activity, checked for polygyne colonies, and recorded various kinds of environmental data. In most areas, we also measured fire ant densities in lawns and grazing land. Fire ant populations along roadsides in North America were 4-7 times higher than fire ant populations in South America. Similar intercontinental differences were found in lawns and on grazing lands. These intercontinental differences in fire ant abundance were not associated with sampling conditions, seasonal variability, habitat differences, or the frequency of polygyny. Although several correlations were found with long-term weather conditions, careful inspection of the data suggests that these correlations were probably more coincidental than causal. Cultural differences in roadside maintenance may explain some of the intercontinental differences in fire ant abundance, but they did not account for equivalent intercontinental differences in grazing land and mowed lawns. Bait tests showed that competition with other ants was much more important in South America; however, we were not able to determine whether this was a major cause of intercontinental differences or largely a consequence of other factors such as the numerous pathogens and parasites that are found in South America. Because this study was correlational, we were unable to determine the cause(s) of the large intercontinental difference in fire ant abundance that we observed. However, we were able to largely exclude a number of possible explanations for the differences, including sampling, season, polygyny, climate, and aspects of habitat. By a process of elimination, escape from natural enemies remains among the most likely explanations for the unusually high densities of fire ants found in North America.