Eastern yellowjacket

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Eastern yellowjacket
48085134.yellowj.web.jpg
Conservation status
Not evaluated (IUCN 3.1)
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Vespidae
Genus: Vespula
Species: V. maculifrons
Binomial name
Vespula maculifrons
(Buysson, 1905)
Synonyms
  • V. flavida Sladen, 1918
  • V. inexpectata Eck, 1994

The Eastern yellow jacket or Eastern yellowjacket (Vespula maculifrons) is a wasp found in eastern North America and throughout the Great Plains region of the United States.[1] Although most of their nests are subterranean, they are often considered a pest due to their nesting in recreational areas and buildings.[2] This yellow jacket is a social insect, living in colonies of hundreds to thousands of individuals.[3] Along with their subfamily, Vespinae, this species demonstrates supportive parental care for offspring, separation of reproductive and sterile castes, and overlapping generations.[4] They will aggressively defend their hive from threats and are known to inflict painful stings.

Taxonomy and phylogenetics[edit]

V. maculifrons is within the family Vespidae, which is commonly found throughout the Northern Hemisphere. The Vespidae family consists of three subfamilies – Stenogastrinae, Polistinae, and Vespinae – which display common features such as tarsal claws. V. maculifrons is part of the Vespinae subfamily, and these species are part of the yellowjackets, distinguished by their black and yellow color.[5] V. maculifrons is commonly called the eastern yellowjacket and found in eastern North America.[6] The species name maculifrons is derived from the Latin word ‘macula,’ which means spot, and ‘frons,’ which means forehead. This refers to the spots on the head of species, which is another distinguishing characteristic. Like other Vespula species, V. maculifrons is a social wasp. As a result, the species participates in cooperative brood care and division between reproductive and non-reproductive groups.[5]

Description and identification[edit]

V. maculifrons can be differentiated from other wasp species due to its smaller size and abdominal pattern.[6] The most recognizable features of V. maculifrons are the black and yellow lines on the head, thorax and abdomen. The body is curved and wider than the head. The abdomen narrows at its attachment to the thorax, which is thinner than the abdomen. The lines on the abdomen also differ based on caste, with the queens having one flared black line nearest the thorax followed by thinner black lines. The queen also has two black dots in between each black line.[5] The individuals of the species range in size from 12.7–15.9 mm (0.5–0.625 in).[7] and weigh roughly 0.04 grams.[8] The queens are the largest, followed by the males and then the workers. A V. maculifrons nest can be anywhere from 9.5 to 30 cm in diameter, allowing for hundreds to thousands of workers inside. A large nest can contain 10,000 to 15,000 cells, with a little less than a third of them dedicated to the larger queen cells.[5] The envelope of the nest is tan-brown to red-orange in color. It is constructed out of worn, decaying wood, which results in a fragile structure.[2] These nests are typically subterranean, but have been found in various site above-ground, including buildings.

Distribution and habitat[edit]

V. maculifrons is commonly found throughout eastern North America to the Great Plains. In most of the areas that it is found, V. maculifrons is the most common yellowjacket species. In the spring, the queen selects the spot where the colony will be located. Their subterranean nests are not deep, mostly covered by less than 5 cm of soil.[2] However, nests have been found anywhere from 0 to 25 cm deep.[2] These nests are found in hardwood forests and creek banks, but also in urban and suburban areas.[5] Within these areas, nests are typically built in sheltered places, which can include under-ground areas, tree stumps, and attics.[2] Their nests are so frequently found in recreational and residential areas that they are seen as a pest problem.

The queen begins the initial structure of the nest. By chewing wood and adding in saliva to make a quick drying pulp, these wasps assemble paper nests. The first part of the nest constructed is the stalk, which eventually narrows into a cord and then expands again to make the first hexagonal cell. Other cells are then added to the sides of the first and an envelope is built around the first group of cells which form a miniature comb. The queen then lays eggs in these cells, which will become workers when hatched. As soon as the workers emerge from their larval state, the nest begins to enlarge rapidly. As more cells are added, the comb grows fast and when there are enough cells on the first comb, a second comb is added, and so on. To make room for more cells, the inner layers of the envelope are re-chewed and used to make more envelope layers outside. Because most of the nests are located underground, the cavity in which the nest is built is enlarged by removing earth, carrying it and dropping it outside of the nest.[9]

Colony cycle[edit]

A colony consists of three types of individuals in a social group: queens, workers, and males. A new colony is started annually during the spring. This is determined by location, but will occur around May or June in the northern regions and around September in southern regions.[8] Due to the seasonal differences, the northern cycle is typically shorter than in the south, resulting in smaller nest sizes.[5] A queen, who mated earlier in the year and spent the winter in diapause, will found a colony by raising the first group of workers.[10] Until the first offspring emerge as adults, the lone queen lays eggs, forages for food, cares for the young, and defends the nest.[11] These workers will maintain and expand the nest when they mature, while the queen will continue to produce more offspring.[10] It will be the workers job to build anywhere from 850 to 9700 cells, of which about 30% are dedicated to queen cells. When these queen cells begin to be constructed, the nest is said to have matured. In the north, colonies will peak around August or September, while southern colonies tend to peak around October to November.[2] When winter comes, the colony demises and only some of the queens will survive to begin a new colony the next nesting cycle.

Behavior[edit]

Communication[edit]

In order for V. maculifrons workers to communicate with others in the nest about a potential predator, they have an alarm pheromone that stimulates defense. This pheromone is linked to the sting apparatus and prompts attraction and attack. When the alarm pheromone is expressed, wasps around the nest entrance are typically seen circling, outlining a zigzagging flight, and going directly towards the target. However, foragers who were not at the nest when the pheromone was expressed did not respond in a similar manner. On the other hand, the facultative social parasite of V. maculifrons, V. squamosa, do respond to the alarm response of V. maculifrons, suggesting common chemistry between pheromones.[12] Since V. squamosa is known to take over nests of V. maculifrons, it would be selected for V. squamosa to be able to recognize and respond to alarm calls within the nest.

Mating behavior[edit]

Male/Male interactions[edit]

Male V. maculifrons tend to form loose aggregations, resembling leks, during mating.[13] In one area, hundreds to thousands of males will patrol prominent trees and bushes by constantly flying around them. Males typically patrol large areas randomly, rather than limiting to a few trees. If a male sees a female while patrolling, he flies closer to the female in a zigzag fashion and stops on a nearby leaf. This then allows the male to climb onto the female’s gaster from behind. Other males do not try to approach an ongoing copulation, but a male might try to copulate immediately after. If a second mating occurs, sperm competition may favor the second male. As a result, males can prevent competition from another male by elongating copulation.[13]

Female/Male interactions[edit]

A queen is capable of mating starting 48 hours after birth. To find a male, queens fly to trees and bushes where males form aggregations. Males frequently groom their legs, antennae, and gasters throughout courtship, mating, and after contact with a queen. The queens have also been seen to groom the face and antennae, but only briefly. At the end of copulation, a queen is able to produce an olfactory or contact pheromone to signal release to the male. The queen also begins to nibble the dorsal surface of the male’s gaster to further signal the end of copulation. Since both queens and males can mate multiple times, the queen’s signals are advantageous if her spermatheca is full, thereby preventing the waste of resources and time. It is also advantageous for the male to have strong genitalic locks for mating, due to male-male competition, but can cause problems during disengagement. In the laboratory, both females and males have died during disengagement, sometimes leaving reproductive ends attached to the opposite sex.[14]

Kin selection[edit]

Genetic relatedness within colonies[edit]

As a social species, V. maculifrons colonies depend on collaboration. However, polyandry tends to create subfamilies with lower relatedness, which can lead to conflict within the colony. Yet, V. maculifrons queens, and many other species’ queens, mate multiply. This occurrence is explained by the fact that potential conflict between subfamilies is offset by the reproductive success of queens; the mate number of queens is correlated to the number of queen cells a colony creates.This phenomenon may occur due to higher genetic diversity, which could lead to genetically varying workers who are more efficient at their jobs.[10]

Kin recognition and discrimination[edit]

As seen in many social insects, cuticular lipids are a source of communication among adults. In general, cuticular lipids function to avoid dehydration by acting as a seal to keep moisture in. However, the hydrocarbons on the surface of cuticular lipids can also serve in identifying the individual’s species, and more importantly, kin. Kin recognition occurs because each species has a unique cuticular hydrocarbon composition. However, the hydrocarbon composition between V. maculifrons and V. squamosa was very similar, which was unexpected because of their differing subgenera. This occurrence is advantageous to V. squamosa because the species is a social parasite of V. maculifrons, and if their hydrocarbon composition is similar, it can act as a chemical camouflage to help V. squamosa parasitize nests. There were also minor differences between the cuticular hydrocarbon compositions between workers and queens.[15]

Worker queen conflict[edit]

When queen cell construction begins in late August to early September, it would be in the male’s best interest to mate with a queen and produce a gyne.[2] Similar wasp species illustrate workers who help their own kin or harm non-relatives from growing as a gyne. Thus, reproductive competition would occur so that the genes of specific subfamilies can be passed on and survive. However, there has been no evidence of reproductive competition within V. maculifrons colonies. Although a second male may occasionally attempt to grasp a queen immediately after copulation with another male, post-copulatory sperm competition is not common. In addition, reproductive skew among males is low.[16]

Life history and survivorship curves[edit]

Towards the end of the seasonal cycle, the gynes mate with multiple males. Then, around November to December, the colony begins to demise.[6] At this point, the queens undergo diapause, which is a dormancy period to avoid the adverse environmental conditions of winter. During these months, only a few queens survive. Those that do typically exhibit larger overall body size as well as a thin shape. However, specific genotypes and previous mating did not affect queen survival during this period.[17] Queen survival is very important because those that survive diapause are able initiate a new colony in the spring.

Interaction with other species[edit]

Diet[edit]

V. maculifrons is a polyphagous species, meaning that they can feed on a variety of food.[18] The number of trips a worker makes to forage depends on the age of the worker as well as the size of the nest, since more food is necessary to feed a larger nest.[19] Workers dedicated to foraging are capable of olfactory learning, allowing them to distinguish odors specific to food.[18] Workers will utilize this ability to scavenge for dead insects like earwigs and fall webworm larvae, as well as live arthropods.[5] They are also frugivores, obtaining carbohydrates from fruits, nectar, and honeydew.[8] Workers go to flowers in attempt to catch insects, but often end up feeding on nectar and pollinating the flower while doing so. They feed on honeydew, which is a sweet, sticky liquid. However, honeydew is susceptible to fermentation, causing individuals who feed on it to become inebriated and unable to fly or walk.[19] Since this species is attracted to sugar sources, they may be attracted to soft drinks or other foods that are consumed by humans.[3] Adults feed larvae with a chewed paste made from other insects as well as carrion.

Predators[edit]

There are many predators to V. maculifrons. Most of the predators are mammals much larger than a V. maculifrons individual, such as raccoons, black bears, and skunks.[2] Raccoons have been found to be one of the main predators in states like Georgia and Indiana.[5] To consume the colony, raccoons dig to uncover the nest, distribute brood cells, and finally scrape individual broods away from the cell using their teeth.[2] Dolichovespula maculate, a hornet species, is another predator to V. maculifrons and other yellowjacket species.[5] Predation of V. maculifrons may occur over other wasp species due to the shallow depths and fragile envelopes of their nests.

Parasites[edit]

Vespula squamosa is a common parasite of V. maculifrons, though they are facultative, which means that they can live both independently as well as parasitically. Roughly 80% of V. squamosa colonies are parasitic, which can be determined if any V. maculifrons workers are present or if the nest itself has the characteristics of a V. maculifrons nest, such as its typical small, tan cells.[5] However, parasitic colonies were not as frequent in areas of unobstructed forest.[2] To become parasitic, a V. squamosa queen forcibly takes control of the nest from the host queen. Then, the host colony’s workers raise the first brood of V. squamosa, until their own workers are mature.[5] Eventually, all V. maculifrons workers will die out.[20]

Commensals[edit]

Commensals, which is a relationship where one organism benefits from living on or with another organism without harm, occurs with two species of muscid flies: Fannia canicularis, which is commonly known as the Lesser house fly, and Dendrophaonia querceti. Females of both species will lay their eggs directly on the outer portion of the nest envelope. Therefore, when the eggs hatch, the larvae will fall into the soil below the nest, where waste products and debris also fall.[2] The larvae will feed on this waste, thereby preventing waste and debris buildup under the nest.

Economic importance[edit]

V. maculifrons destroy many insects that consume cultivated and ornamental plants, providing a valuable service to humans. They can, however, be a source of irritation when their nests are located near homes. V. maculifrons are adept at stinging, especially if the nest is threatened. Not to be confused with certain bees that die after a single sting, these wasps may sting repeatedly whenever they feel it necessary and can inflict a very painful sting.[3]

References[edit]

  1. ^ Hoffman, Eric A., Kovacs, Jennifer L. and Goodisman, Michael A. D. (August 20, 2008). Genetic structure and breeding system in a social wasp and its social parasite. BMC Evolutionary Biology.
  2. ^ a b c d e f g h i j k MacDonald, J. F., and R. W. Matthews. "Nesting Biology of the Eastern Yellowjacket, Vespula Maculifrons (Hymenoptera: Vespidae)." Journal of the Kansas Entomological Society 54.3 (1981): 433-57. JSTOR. Web. 22 Sept. 2014. <http://www.jstor.org/stable/25084177>.
  3. ^ a b c Yellowjackets and Hornet Vespula and Dolichovespula spp. (Insecta: Hymenoptera: Vespidae). Grissell, E. E. and Fasulo, Thomas R. 2007, University of Florida IFAS Extension, pp. 1-5.
  4. ^ Identification Atlas of the Vespidae (Hymenoptera, Aculeata) of the northeastern Nearctic region. Buck, Matthias, Marshall, Stephen A. and Cheung, David K. B. 2008, Canadian Journal of Arthropod Identification No. 5, pp. 20-21; 402-403.
  5. ^ a b c d e f g h i j k 12 Greene, Albert, John F. Macdonald, Peter J. Landolt, and Harry G. Davis. "Biology." The Yellowjackets of America North of Mexico. By Roger D. Akre. Washington, D.C.: U.S. Dept. of Agriculture, 1980. 3+. Print.
  6. ^ a b c Grissell, E. E., and Thomas R. Fasulo. "Yellowjackets and Hornets, Vespula and Dolichovespula Spp. (Insecta: Hymenoptera: Vespidae)." DPI Entomology Circular 142 (1999): 1-4. Web. 24 Sept. 2014. <http://edis.ifas.ufl.edu/pdffiles/IN/IN23800.pdf>.
  7. ^ Milne, Lorus and Milne, Margery. (1980). Yellow Jackets. The Audubon Society Field Guide to North American Insects and Spiders. s.l. : Alfred A. Knopf, Inc. pp. 836-837.
  8. ^ a b c Coelho, J.r., and A.j. Ross. "Body Temperature and Thermoregulation in Two Species of Yellowjackets, Vespula Germanica and V. Maculifrons." Journal of Comparative Physiology B 166.1 (1996): 68-76. Academia.edu. Web. 22 Sept. 2014. <http://www.academia.edu/836035/Body_temperature_and_thermoregulation_in_two_species_of_yellowjackets_Vespula_germanica_and_V._maculifrons>.
  9. ^ Andrews, Christopher. (1971). The Lives of Wasps and Bees. New York:American Elsevier Publishing Company, Inc. pp.100-107.
  10. ^ a b c Goodisman, Michael A. D., Jennifer L. Kovacs, and Eric A. Hoffman. "The Significance Of Multiple Mating In The Social Wasp Vespula Maculifrons." Evolution 61.9 (2007): 2260-267. Wiley Online Library. Web. 22 Sept. 2014. <http://onlinelibrary.wiley.com/doi/10.1111/j.1558-5646.2007.00175.x/full>.
  11. ^ Evans, Howard E. and West Eberhard, Mary Jane. The Wasps. Ann Arbor : The University of Michigan Press, 1970.
  12. ^ Landolt, P. J., R. R. Heath, H. C. Reed, and K. Manning. "Pheromonal Mediation of Alarm in the Eastern Yellowjacket (Hymenoptera: Vespidae)." The Florida Entomologist 78.1 (1995): 101-08. JSTOR. Web. 22 Sept. 2014. <http://www.jstor.org/stable/3495673>.
  13. ^ a b Post, David C. "Observations on Male Behavior of the Eastern Yellowjacket, Vespula Maculifrons (Hymenoptera: Vespidae)." Entomological News 91.4 (1980): 113-16. Internet Archive. Web. 22 Sept. 2014. <http://www.archive.org/details/cbarchive_119394_observationsonmalebehaviorofth1925>.
  14. ^ Ross, Kenneth G. "Laboratory Studies of the Mating Biology of the Eastern Yellowjacket, Vespula Maculifrons (Hymenoptera: Vespidae)." Journal of the Kansas Entomological Society 56.4 (1983): 523-37. JSTOR. Web. 22 Sept. 2014. <http://www.jstor.org/stable/25084456>.
  15. ^ Butts, Douglas P., Karl E. Espelie, and Henry R. Hermann. "Cuticular Hydrocarbons of Four Species of Social Wasps in the Subfamily Vespinae: Vespa Crabro L., Dolichovespula Maculata (L.), Vespula Squamosa (Drury), and Vespula Maculifrons (Buysson)." Comparative Biochemistry and Physiology Part B: Comparative Biochemistry 99.1 (1991): 87-91. Web. 22 Sept. 2014. <http://ac.els-cdn.com/0305049191900123/1-s2.0-0305049191900123-main.pdf?_tid=7874e64a-4435-11e4-a97d-00000aacb360&acdnat=1411595897_3c9f713cc1f0d051323806b88701ba07>.
  16. ^ Goodisman, Michael A. D., Jennifer L. Kovacs, and Eric A. Hoffman. "Lack of Conflict during Queen Production in the Social Wasp Vespula Maculifrons." Molecular Ecology16 (2007): 2589-595. Wiley Online Library. Web. 22 Sept. 2014. <http://onlinelibrary.wiley.com/store/10.1111/j.1365-294X.2007.03316.x/asset/j.1365-294X.2007.03316.x.pdf?v=1&t=i0h819xz&s=96b3381872cb772244e1edc0427fc380e78e7586>.
  17. ^ Kovacs, Jennifer L., and Michael A. D. Goodisman. "Effects of Size, Shape, Genotype, and Mating Status on Queen Overwintering Survival in the Social Wasp Vespula Maculifrons." Environmental Entomology 41.6 (2012): 1612-620. BioOne. Web. 22 Sept. 2014. <http://www.bioone.org/doi/full/10.1603/EN12023>.
  18. ^ a b Jander, Rudolf. "Olfactory Learning of Fruit Odors in the Eastern Yellow Jacket, Vespula Maculifrons (Hymenoptera: Vespidae)." Journal of Insect Behavior 11.6 (1998): 879-88. Springer. Web. 22 Sept. 2014. <http://link.springer.com/article/10.1023/A:1020868311982>.
  19. ^ a b Edwards, Robin. "The Behaviour of Workers outside the Nest." Social Wasps: Their Biology and Control. East Grinstead: Rentokil, 1980. 120-45. Academia.edu. Web. 23 Sept. 2014. <http://www.academia.edu/2325339/Edwards_1980_Social_Wasps_Their_Biology_and_Control>.
  20. ^ Mcdonald, J. F., and R. W. Matthews. "Vespula Squamosa: A Yellow Jacket Wasp Evolving Toward Parasitism." Science 190.4218 (1975): 1003-004. Academia.edu. Web. 22 Sept. 2014. <http://www.academia.edu/3404263/Macdonald_and_Matthews_1975_Vespula_squamosa_A_yellowjacket_wasp_evolving_toward_parasitism>.

External links[edit]