Mischocyttarus Mexicanus

''Mischocyttarus mexicanus'' (de Saussure) is a New World paper waspPost, DC & Jeanne, RL. (1982). "Sternal Glands in Three Species of Male Social Wasps of the Genus ''Mischocyttarus'' (Hymenoptera: Vespidae)." ''Journal of the New York Entomological Society''. 90(1):8–15. that exhibits facultative eusocial behavior and includes at least two subspecies living in the southern United States and Central America.Gunnels IV, CW, Dubrovskiy, A, & Avalos, A. (2008). "Social interactions as an ecological constraint in a eusocial insect." ''Animal Behavior''. 75:681–691. This social wasp species is a good model for studying the selective advantage of different nesting tactics within a single species.Clouse, R. (2001). "Some effects of group size on the output of beginning nests of ''Mischocyttarus mexicanus'' (Hymenoptera: Vespidae)." ''Florida Entomologist''. 84(3):418–424. ''M. mexicanus'' females can form nests both as individuals and as members of a colony, and are even known to switch between these two nesting strategies throughout their life, which is an unusual phenomenon in the field of social biology. Individuals in a colony have particular social roles that are plastic, as opposed to rigid castes, and brood parasitism and usurpation have been observed between unrelated conspecifics. They nest in a variety of types of plants and human constructions, although they have most frequently been observed in palm trees, and they are known to interact with a number of other species as prey, competitors over resources, or foragers.

Taxonomy and phylogeny

''M. mexicanus'' was described by Henri de Saussure in 1854, and it is a member of the social polistine wasp genus '' Mischocyttarus''.Silveira, OT. (2008). "Phylogeny of wasps of the genus ''Mischocyttarus'' de Saussure (Hymenoptera, Vespidae, Polistinae)." ''Revista Brasileira de Entomologia''. 52(4):510–549. ''Mischocyttarus'' is actually cited as the largest genus of social wasps, and it consists entirely of New World wasp species. ''M. mexicanus'' includes at least two subspecies: ''M. mexicanus cubicula'' (Richards, 1978) and ''M. mexicanus mexicanus'' (de Saussure).Carpenter, JM, Hunt, JH, Strassmann, JE. (2009). "''Mischocyttarus mexicanus cubicola'': Major Extension of Its Range to Texas (Hymenoptera: Vespidae)." ''Entomologica Americana''. 115(1):95–96. ''Mischocyttarus'' biology is, reportedly, very similar to that of several wasps of the genus ''Polistes''.

Description and identification

The genus ''Mischocyttarus'' is recognized by having asymmetrical internal and external lobes of the tarsal segments in adults and by appendix-like projections extending forward from the abdominal sternum of mature larvae. ''M. mexicanus'' belongs to a group of species within the genus that all share certain similarities, which includes ''Mischocyttarus flavitarsis'' and ''Mischocyttarus angulatus''. This group of species is known for having a sharp secondary margin on their pronotum, which is the dorsal surface of the prothorax. In addition, males have very short, thick antennae. Females also have a clypeus, or head plate, with a flattened apex. ''M mexicanus'' typically has an orange-yellow color.Landolt, PJ, Gonzalez, M, Chambers, DL, & Heath, RR. (1991). "Comparison of Field Observations and Trapping of Papaya Fruit Fly in Papaya Plantings in Central America and Florida." ''The Florida Entomologist''. 74(3):408–414.

Distribution and habitat

''M. mexicanus'' is a New World wasp species found anywhere from the southern United States to Costa Rica. Subspecies ''M. m. mexicanus ''is predominantly present anywhere between Mexico and Costa Rica, though it has been sighted in Texas. On the other hand, the subspecies ''M. m. cubicola'' has been observed in the southeastern U.S., the Bahamas, Cuba, Puerto Rico, Texas, and Missouri. ''M. m. cubicola'' has been seen in almost every county of Florida except for the most northwestern counties of the state. It has been proposed that there is a distribution barrier that runs through northwestern Florida preventing the spread of ''M. m cubicola'' west of Alabama.Hermann, HR & Chao, JT. (1984). "Distribution of ''Mischocyttarus (Monocyttarus) mexicanus cubicola'' in the United States." ''The Florida Entomologist''. 67(4):516–520. However, this subspecies was observed in Texas and Missouri in 2009 nesting in a number of palm species, other trees, and human constructions.

Colony cycle

The colony cycle of ''M. mexicanus'' was detailed extensively by Marcia Litte in the 1970s.Strassmann, JE, Queller, DC, & Solís, CR. (1995). "Genetic relatedness and population structure in the social wasp ''Mischocyttarus mexicanus'' (Hymenoptera: Vespidae)." ''Insectes Sociaux''. 42:379–383. The nests of ''M. mexicanus'' can be founded by one to twenty females, and while there is an "early" and "late" period for nests, they can be initiated at any point during the year. The founders of a nest are typically born together, and they do not range far from their natal nest site. There is a range in the sexual development of females, and each nest can have one or more queen. However, most females are reproductively viable and are capable of becoming a queen. The nests include a comb consisting of open cells made of paper, and are attached to leaves by a stem. The life cycle of a nest can be divided into pre-daughter or post-daughter stages,Litte, M. (1977). "Behavioral Ecology of the Social Wasp, ''Mischocyttarus mexicanus''." ''Behavioral Ecology and Sociobiology''. 2(3):229–246. or sometimes referred to as pre-eclosion and post-eclosion nests. The duration of a nest is estimated at 8 months, although a large percentage of nests fail long before then.

Behavior

Nesting tactics

''M. mexicanus'' has been found to have two stable nesting strategies: haplometrosis and pleometrosis. Haplometrosis refers to the single-foundress nesting strategy, while pleometrosis refers to a strategy involving multiple cofoundresses. Both of these tactics are stable in ''M. mexicanus'' and it has been found that this is because each of these strategies is favorable in certain conditions, so this is an example of a context-dependent trait. Haplometric nests are more susceptible to greater mortality, and indeed up to 80% of haplometrotic nests fail within 20 days. However, haplometrosis has been found to be more frequent in the winter and spring, while pleometrosis is more frequent during the fall. It has been proposed that larger females are more likely to be solitary foundresses in the spring, and group foundresses in the summer, which a preference not found in smaller females.Gunnels IV, CW. (2007). "Seasonably Variable Eusocially Selected Traits in the Paper Wasp, ''Mischocyttarus mexicanus''." ''Ethology''. 113:648–660. Additionally, when the number of potential habitats is experimentally decreased in an area, then nests are more likely to be founded by multiple females, and the converse has been found to hold true as well, indicating that these nesting tactics are context-dependent. Additionally, a female can switch between nesting tactics as an adult, suggesting that this trait is plastic.

Nest construction

Nests of ''M. mexicanus'' have been observed on saw palmetto (''Serenoa repens''), cabbage palm (''Sabal palmetto''), oak trees, Spanish moss, and human constructions. Fiber sources for the paper nests are often located rather close to the nest compared to food sources. However, it has been found that ''M. mexicanus'' nests are often constructed on the eastern-facing side of palm fronds, probably because this orientation increases the activity of the nest early in the day, as a consequence of the increased luminance and temperature. It was also found that foundresses preferred the outside curl of palm fronds over the inside curl and that the cabbage palm may provide greater protection against birds than other habitats.Hermann, HR, Gonzalez, JM, & Hermann, BS. (1985). "''Mischocyttarus mexicanus cubicola'' (Hymenoptera), Distribution and Nesting Plants." ''The Florida Entomologist''. 68(4):609–614.

Social structure

''M. mexicanus'' females in a colony are at various levels of ovary development, and though there is typically one or more queen per colony, a relatively large proportion of females are reproductively viable. Females within a nest have been found to be highly variable, in that after a nest is initiated, one female may become the primary reproductive female, and the others may become subordinates.Mora-Kepfer, F. (2014). "Context-dependent acceptance of non-nestmates in a primitively eusocial insect." ''Behavioral Ecology and Sociobiology''. 68:363–371. However, nest switching is frequent, and if a queen is removed, then a nestmate may replace her within the span of a week. The females in any given nest have a surprisingly low level of relatedness. Some reasons why ''M. mexicanus'' nests would be pleiotropic in spite of this low relatedness include reduced mortality rates of multiple-foundress nests, reduced development times, and larger colony sizes.

Cannibalism and usurpation

It has been observed that upon removal of a queen from the nest, the larvae and eggs gradually disappear over the course of a week. During this period no new cells of the nest are constructed, and at the end of this period, a subordinate wasp from the nest may begin to lay eggs and become the queen. It was also observed that non-nestmates are accepted into the colony when the foreign wasp is young, and when the nest itself is relatively new. However, an older wasp is often prevented from joining a colony, and older nests tend to reject non-nestmates of any age. These observations lead to speculation that ''M. mexicanus'' individuals reject foreigners based on the risk that they may usurp their nest. Intercolonial cannibalism was found to occur in nests, and foreign conspecific females may intrude on any given nest at a rate of once every 5 hours.Clouse, RM. (1995). "Nest Usurpation and Intercolonial Cannibalism in ''Mischocyttarus mexicanus'' (Hymenoptera: Vespidae)." ''Journal of the Kansas Entomological Society''. 68(1):67–73. Additionally, it is possible that ''M. mexicanus'' females may be brood parasites, cannibalizing eggs of a foreign nest and placing an egg of their own in the empty cell.

Interaction with other species

Predators

Birds are a major source of predation on ''M. mexicanus''. Carolina wrens, scrub jays, blue jays, common yellowthroats, cardinals, thrashers, mockingbirds, woodpeckers, and robins are suspected to be predators of this species and are thought to destroy nests. Additionally, spiders such as orb weavers ''Argiope aurantia'' and ''Nephila clavipes'' are thought to be predators of ''M. mexicanus''.

Ants are commonly found raiding nests of this species, though it is rare that ants will raid a nest that hasn’t already been abandoned. Species including ''Campanotus floridanus'', '' Crematogaster ashmeadi'', and ''Pheidole floridana'' are known to raid live nests and eat the brood of the wasp colony. However, it was found that most commonly, a single ant will encounter a nest and be successfully deterred.

Other wasps

Apart from the conspecific interactions that are discussed above, it is expected that ''M. mexicanus'' competes with other wasp species for nesting places. It was found that nesting areas of ''M. mexicanus'' were mutually exclusive with ''Polistes exclamans'' and '' P. metricus'', two sympatric wasp species that are also known to nest in similar habitats.

Mimicry

The papaya fruit fly, ''Toxotrypana curvicauda'', has evolved different color variations in populations living in distinct geographic regions. In the areas of Florida that it shares with ''M. mexicanus'', it has been found to have a brown and dark orange-yellow color, which is similar to ''M. mexicanus''. The females have a long ovipositor which is often mistaken as a stinger, and increases the resemblance of this species to ''M. mexicanus'' and other similar wasp species.Landolt, PJ. (2000). "Chapter 14: Behavior of Flies in the Genus ''Toxotrypana'' (Trypetinae: Toxotrypanini)." In Aluja, M, Norrbom AL. (Eds.). ''Fruit Flies (Tephritidae): Phylogeny and Evolution of Behavior'' (363–373). Boca Raton, Florida: CRC Press LLC. Print. It appears that the fruit flies also mimic certain defensive behaviors of wasps. When being handled by humans, the flies often curve their bodies and appear as if they are attempting to use their ovipositor as a stinger. The selective advantage of this morphological and behavioral mimicry has not yet been fully elucidated.

Communication

Biting has been found to be a frequent occurrence between nestmates. The individuals that do the most foraging in a multi-foundress colony were found to be the least aggressive individuals of the group. It was also found that the individuals with the least developed ovaries were the individuals that did the most foraging of the group. Additionally, there has been speculation that ''M. mexicanus'' individuals accumulate a particular odor as they age, which is consistent with the observation that older females are more often rejected by foreign nests.Neves, EF, Andrade, LHC, Súarez, YR, Lima, SM, & Antonialli-Junior, WF. (2012). "Age-related changes in the surface pheromones of the wasp ''Mischocyttarus consimilis'' (Hymenoptera: Vespidae)." ''Genetics and Molecular Research''. 11(3):1891–1898. Males were found to have exocrine gland cells in their gastral sternites, though they have very few ducted exocrine gland cells when compared to other species of ''Mischocyttarus''. However, these observations are consistent with the idea that ''M. mexicanus'', like other wasps, use chemicals to communicate through nestmate recognition, pheromone signaling, etc.

Diet

''M. mexicanus'' was found to forage both arthropod and nectar-based foods. It is suspected that they prey on arthropod larvae. Additionally, females have been observed foraging on palmetto and '' Lyonia'' flowers. Males are also commonly found on flowers, and they often pounce on other ''M. mexicanus'' individuals that are foraging on those flowers, which is presumably related to the mating habits of this species.

References

{{Taxonbar, from=Q14424227

Vespidae
Hymenoptera of North America
Insects described in 1854
Insects of Central America