The Mutillidae are a family of wasps whose wingless females resemble large, hairy ants

The Mutillidae are a family of more than 7,000 species of wasps whose wingless females resemble large, hairy ants. Their common name velvet ant refers to their dense pile of hair, which most often is bright scarlet or orange, but may also be black, white, silver, or gold. Their bright colors serve as aposematic signals. North American Mutillidae have eight phenotypically distinct and geographically limited Müllerian mimicry rings (Desert, Eastern, Madrean, Texan, Red-headed Timulla, Black-headed Timulla, Tropical, and Western) making up one of the largest Müllerian mimicry complexes on the planet. These mimicry rings are the result of repeated convergent evolution of aposematic traits between co-occurring velvet ant species, rather than shared, phylogenetic history. Through the evolution of aposematic traits in velvet ant species in the same ring, local predators have learned to avoid this well-defended species. Adult mutillids feed on nectar. Although some species are strictly nocturnal, females are often active during the day. Females of Tricholabiodes thisbe are sometimes active up to two hours before sunset. Guido Nonveiller (1963) hypothesized the Mutillidae are generally stenothermic and thermophilic; they may not avoid light, but rather are active during temperatures that usually occur only after sunset. The venom that velvet ants inject through their stinger has an unknown composition. According to one researcher, the painfulness of the sting of Dasymutilla klugii outscored 58 other species of stinging insects tested; the only species this researcher rated as having a more painful sting were the Paraponera clavata (bullet ant), Synoeca septentrionalis (warrior wasp), Pepsis spp. and Hemipepsis spp. (tarantula hawks). In an experimental setting, only two lizard species (one whiptail and one side-blotched lizard) attacked a velvet ant it was exposed to. In both cases the velvet ants were exhibiting rapid lateral and vertical movements to ward off an attack. Once the attack occurred the velvet ants would immediately sting the lizards. This sting resulted in the dropping of the ants in both cases and avoidance for the remainder of the trial. The side-blotched lizard was found dead in its tank 24 hours later. The side-blotched lizard is a natural predator of velvet ants, while the whiptail is not. The aposematic coloration of velvet ants often corresponds to a specific Müllerian mimicry ring consisting of dozens of species. This offers protection because many local predators have learned to avoid prey with this same coloration. To test the aposematic coloration on birds, mealworms were painted to resemble a velvet ant. During these trials, none of the painted mealworms were consumed, while all the control mealworms were consumed immediately. However, the painted mealworms were attacked by the birds, but the birds immediately ceased the attack. The stridulatory organ that velvet ants possess produces an audible squeaking when the abdomen is contracted. This mechanism is an auditory cue warning predators that are about to attack to stay away. In shrews, every time they would get within 1 meter of a velvet ant, the velvet ant would begin stridulating. Stridulations became more frequent as the predator moved closer to the velvet ant, and the shrew never attempted to attack the velvet ant. However, different scenarios with shrews have shown that the velvet ant would also stridulate after the shrew attacked it. Every time this occurred the shrew dropped the wasp. The exoskeleton of the velvet ant is remarkably strong. When compared to the exoskeleton of a honeybee, the velvet ant’s required 11 times more force to crush using a force transducer. As well as being durable, the exoskeleton is also round, making it more difficult for predators to pierce it with attempted stings or bites. During all the trials that led to the fracture of a velvet ant’s exoskeleton, a total of 4 times, resulted in the death of that velvet ant within 24 hours. Aside from protection from predators, the exoskeleton also serves a function in maintaining moisture control. Due to these strong defense mechanisms, local predators generally avoid the velvet ants, so it has been difficult to determine their predators. One study found tropical/ subtropical iguan Male mutillids fly in search of females; after mating, the female enters a host insect nest, typically a ground-nesting bee or wasp burrow, and deposits one egg near each larva or pupa. Only a few species are known to parasitize other types of hosts; exceptions include the European velvet ant, Mutilla europaea, one of the only species that attacks social bees (e.g., Bombus), and the genus Pappognatha, whose hosts are tree-dwelling orchid bees. The mutillid larvae then develop as idiobiont ectoparasitoids, eventually killing their immobile larval/pupal hosts within a week or two. Velvet ants exhibit haplodiploid sex determination, as do other members of the su