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Contents

   



(Top)
 


1 Description  





2 Biochemistry  





3 Life cycle  



3.1  Founding (or pre-emergence) phase  





3.2  Worker phase  





3.3  Reproductive phase  





3.4  Intermediate phase  







4 Behavior  



4.1  Kin selection  





4.2  Dominance hierarchy system  





4.3  Nestmate recognition  







5 Gallery  





6 Species  





7 Pest status  





8 Parasites  





9 References  





10 Further reading  





11 External links  














Polistes






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Polistes
Polistes gallicus
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Vespidae
Subfamily: Polistinae
Tribe: Polistini
Genus: Polistes
Latreille, 1802
Type species
Polistes gallicus

Linnaeus, 1767 [1]

Synonyms[2]
  • Eupolistes Dalla Torre, 1904
  • Sulcopolistes Blüthgen, 1938
  • Polistula Weyrauch, 1939
  • Pseudopolistes Weyrauch, 1939
  • Leptopolistes Blüthgen, 1943
P. metricus, female

Polistes is a cosmopolitan genus of paper wasps and the only genus in the tribe Polistini. Vernacular names for the genus include umbrella wasps, coined by Walter Ebeling in 1975 to distinguish it from other types of paper wasp, in reference to the form of their nests,[3] and umbrella paper wasps.[4] Polistes is the single largest genus within the family Vespidae, with over 200 recognized species.[5] Their innate preferences for nest-building sites leads them to commonly build nests on human habitation, where they can be very unwelcome; although generally not aggressive, they can be provoked into defending their nests. All species are predatory, and they may consume large numbers of caterpillars, in which respect they are generally considered beneficial.[citation needed]

Description[edit]

As part of subfamily Polistinae, Polistes wasps are covered in short and inconspicuous hair, have a clypeus with a pointed apex, have a gena that is wide throughout, tergum 1 of the metasoma is almost straight to gently arched in profile, the tibia of the mid leg has two spurs, and the legs end in simple tarsal claws. The genus can be distinguished from other Polistinae by a sessile metasoma (the first segment at most slightly longer than wide) and the fourth tarsomeres of the mid and hind legs being symmetrical.[6]

Polistes show sexual dimorphism, with males having seven externally visible metasomal segments whereas females have six. This trait is shared with other vespid wasps.[6]

Polistes species have single-layered nests which are shaped like an umbrella, with the cells exposed to the air from the bottom, and no layer wrapping around the nest. The nests are suspended from a surface by a petiole and are constructed from a paper-like substance made of a mix of saliva and wood fibres chewed off old and soft wood or dead twigs. Many Polistes species in general often have nests supported by a longer petiole than those of Vespula.[3]

Biochemistry[edit]

Similar to many insects, Carlson et al 1998 finds Polistes cuticular hydrocarbons to be predominantly many branched, methyl branched alkanes. The reviews of Nelson 1978, Lockey 1988 and Nelson 1993 concur.[7]

Life cycle[edit]

The general life cycle of Polistes can be divided into four phases:[8]

  1. Founding (or pre-emergence) phase
  2. Worker phase
  3. Reproductive phase
  4. Intermediate phase

Founding (or pre-emergence) phase[edit]

The founding stage begins in the spring when a solitary female (the "foundress") (or a small group of related females) initiates the construction of a nest. The wasps begin by fashioning a petiole, a short stalk which will connect the new nest to a substrate (often the eave of a house or outbuilding), and building a single brood cell at the end of it. Further cells are added laterally in a hexagonal pattern, each cell surrounded by six others. Although nests can achieve impressive sizes, they almost always maintain a basic shape: petiolated (stellocyttarous), single-combed, unprotected, and open (gymnodomous).

Eggs are laid by the foundress directly into the brood cells and are guarded by the foundress and the assisting females (if present). After the first larvae hatch, the foundress feeds them via progressive provisioning, bringing softened caterpillar flesh to the larvae multiple times throughout their development (as opposed to the one-time provisioning seen in some other hymenopteran groups). Each of this first seasonal brood of new paper wasps is exclusively female and destined to a subordinate worker position inside the nest; they do not found their own nests and instead assist their mother in the care and maintenance of future sisters.

Some foundress wasps do not build their own nests, but rather attempt to usurp that of another female. These usurpation attempts may or may not be successful, but almost always result in impressive displays of aggression and violence. Females may also adopt a more peaceful alternative reproduction strategy by joining the nest of a close relative (usually a sister) and working as assisting females. In the latter case, such cofounding females are generally, but not exclusively, close relatives.[8]

Worker phase[edit]

The worker phase usually begins in the early summer, roughly two months after colony initiation, with the emergence of the first workers. These new females take up most of the colony's work duties, foraging, caring for brood, and maintaining the structure of the nest. Around this time, those females which assisted in nest foundation (if present) are driven from the nest by aggressive behavior on the part of the foundress, and leave either to start their own late-season nests or usurp another's.[citation needed]

Reproductive phase[edit]

The reproductive phase of the colony begins when the first female reproductives (the gynes) emerge from their brood cells. These reproductives differ from their worker sisters by having increased levels of fat stores and cryoprotectant carbohydrate compounds (allowing them to survive the overwintering period). These reproductives contribute genes directly to the next generation, while their worker sisters normally pass along their genes indirectly.[citation needed]

Intermediate phase[edit]

Once male reproductives emerge and both males and females disperse from the natal nest for mating flights, the so-called intermediate phase begins. Brood care and foraging behavior decline and worker numbers drop as dying individuals are no longer replaced by new ones. Intracolonial aggression increases and the social cohesion of the nest declines. In temperate Polistes species, individuals (almost exclusively inseminated females) gather in groups of up to 50 individuals and seek a sheltered location (called a hibernaculum) in which to overwinter.[citation needed]

Behavior[edit]

Kin selection[edit]

The reproductive behavior of Polistes wasps provided some of the first evidence for the mathematical biologist W. D. Hamilton's 1964 theory of kin selection. Hamilton showed that animals such as workers could be expected to provide assistance to relatives such as their queens according to the costs and benefits involved (K) and their degree of genetic relatedness (r), and gave the rule that now carries his name, K > 1/r.[9] Early caution existed among researchers as to whether social insects could really assess their relatedness. Hamilton himself suggested an alternative possibility, namely that kin could become associated simply by "population viscosity" —that offspring tend not to disperse far from their birthplaces— and West-Eberhard (1969) found some evidence for this in Polistes. However, Polistes species are now known to learn and remember chemical signals (hydrocarbons) picked up from the nest to distinguish nestmates accurately from non-relatives.[10]

Dominance hierarchy system[edit]

Morphologically, the foundress and subordinate reproductive members of the colony differ little. However, behavioral differentiation occurs among females both between and within generations. For example, in the species Polistes humilis the queen displays a "tail-wagging" behavior to assert her dominance over the worker class.[11] Similarly, Polistes canadensis also possesses behavioral differentiation between the queen and her nestmates, with the queen often suppressing the aggressive behavior of subordinates through lateral abdominal vibrations and stroking. In contrast, unmated females are not aggressive.[12]InPolistes exclamans queens have different amounts of glucose, fructose, and trehalose which lead to different cryoprotectant levels. This alters their survivability in different temperatures, increasing their odds of reproduction. Females in P. bellicosus are also morphologically similar between caste separations. For example, a P. bellicosus worker could become queen, and egg-layer, if all of the original foundresses die or leave the nest.[13] This is also true for Polistes dorsalis, which also displays dominant behavior. Despite having no distinct morphological caste, roles of P. dorsalis tend to be fixed in a system with division of labor.[14]

Nestmate recognition[edit]

Polistes spp. discriminate colony mates using an acquired (i.e. learned) cue, absorbing hydrocarbons from the natal nest at eclosion.[15] This cuticular hydrocarbon "signature" is derived both from the plant material and the foundress-applied substances from which the nest is made. Studies of Polistes fuscatus have researched the molecular basis of the recognition "pheromone" used by the wasps, and indicate at least some of the recognizable labels have the same chemical constituents as the adult cuticular hydrocarbons. Similar recognition is found in Polistes metricus. [16] Dominant individuals of P. dominula have differing cuticular profiles from workers,[17] and the frequent observations of the dominant female stroking its gaster across the nest surface, combined with its staying on the nest for longer times than subordinates, suggests the dominant individual may contribute more to the nest odor.[citation needed]

P. carolina females do not preferentially feed their own progeny (as larvae).[18]

Further to this recognition of nestmates, Polistes biglumis foundresses discriminate between 'alien' eggs and their own via differential oophagy.[19]

Gallery[edit]

Species[edit]

203 species were described in the genus by 1996,[5] and new species continue to be described.[20] There are nine species in Europe.[2]

224 species and 126 subspecies are as follows:[21][20][22][23]

  • Polistes adelphus Richards, 1978
  • Polistes adustus Bingham, 1897
  • Polistes affinis Gusenleitner, 2006
  • Polistes africanus Palisot de Beauvois, 1818
  • Polistes albicinctus de Saussure, 1890
  • Polistes albocalcaratus du Buysson, 1905
  • Polistes angulinus Richards, 1951
  • Polistes angusticlypeus Gusenleitner, 2006
  • Polistes annularis (Linnaeus, 1763)
  • Polistes apachus (de Saussure, 1857)
  • Polistes apicalis de Saussure, 1858
  • Polistes aquilinus du Buysson, 1905
  • Polistes arizonensis Snelling, 1954
  • Polistes arthuri Cameron, 1901
  • Polistes assamensis Bingham, 1897
  • Polistes associus Kohl, 1898
  • Polistes asterope Cameron, 1901
  • Polistes aterrimus de Saussure, 1853
  • Polistes atrimandibularis Zimmermann, 1930
  • Polistes atrox Richards, 1978
  • Polistes aurifer de Saussure, 1853
  • Polistes austroccidentalis Van Achterberg & Neumeyer, 2017[23]
  • Polistes badius Gerstaecker, 1871
  • Polistes bahamensis Bequaert & Salt, 1931
  • Polistes balder Kirby, 1888
  • Polistes bambusae Richards, 1978
  • Polistes bellicosus Cresson, 1872
  • Polistes bequaertellus Snelling, 1983,
  • Polistes bequaerti von Schulthess, 1921
  • Polistes bequaertianus Willink, 1954
  • Polistes bicolor Lepeletier, 1836
  • Polistes biglumis (Linnaeus, 1758)
  • Polistes biguttatus Haliday, 1836
  • Polistes billardieri Fabricius, 1804
  • Polistes binotatus de Saussure, 1853
  • Polistes bischoffi Weyrauch, 1937
  • Polistes bituberculatus du Buysson, 1905
  • Polistes boharti Snelling, 1983
  • Polistes brevifissus Richards, 1978
  • Polistes brunus Nguyen & Carpenter, 2017[24]
  • Polistes bucharensis Petersen, 1990[23]
  • Polistes buruensis Erichson, 184
  • Polistes buyssoni Brèthes, 1909
  • Polistes callimorphus de Saussure, 1853
  • Polistes canadensis (Linnaeus, 1758)
  • Polistes candidoi von Ihering, 1903
  • Polistes capnodes van der Vecht, 1972
  • Polistes carnifex (Fabricius, 1775)
  • Polistes carolina (Linnaeus, 1767)
  • Polistes cavapyta de Saussure, 1853
  • Polistes cavapytiformis Richards, 1978
  • Polistes chinensis (Fabricius, 1793)
  • Polistes cinerascens de Saussure, 1854
  • Polistes claripennis Ducke, 1904
  • Polistes clavicornis van der Vecht, 1972
  • Polistes comanchus de Saussure, 1857
  • Polistes communalis Nguyen, Vu, & Carpenter, 2017[24]
  • Polistes consobrinus de Saussure, 1858
  • Polistes contrarius Cheesman, 1951
  • Polistes crinitus (Felton, 1765)
  • Polistes cubensis Lepeletier, 1836
  • Polistes davillae Richards, 1978
  • Polistes dawnae Dover & Rao, 1922
  • Polistes deceptor Schulz, 1905
  • Polistes defectivus Gerstaecker, 1871
  • Polistes delhiensis Das & Gupta, 1984
  • Polistes diabolicus de Saussure, 1853
  • Polistes diakonovi Kostylev, 1940
  • Polistes dominicus (Vallot, 1802)
  • Polistes dominula (Christ, 1791)
  • Polistes dorsalis (Fabricius, 1775)
  • Polistes ebsohinus Sonan, 1943
  • Polistes eburneus Bequaert, 1943
  • Polistes elegans Smith, 1859
  • Polistes ellenbergi du Buysson, 1908
  • Polistes ephippium Cameron, 1900
  • Polistes erythrinus Holmgren, 1868
  • Polistes erythrocephalus Latreille, 1813
  • Polistes exclamans Viereck, 1906
  • Polistes extraneus Kirby, 1883
  • Polistes facilis de Saussure, 1853
  • Polistes fastidiosus de Saussure, 1853
  • Polistes ferreri de Saussure, 1853
  • Polistes flavobilineatus (Cameron, 1902)
  • Polistes flavus Cresson, 1868
  • Polistes foederatus Kohl, 1898[23]
  • Polistes fordi van der Vecht, 1972
  • Polistes formosanus Sonan, 1927
  • Polistes franciscanus Richards, 1978
  • Polistes fuscatus (Fabricius, 1793)
  • Polistes gallicus (Linnaeus, 1767)
  • Polistes geminatus Fox, 1898
  • Polistes gigas (Kirby, 1826)
  • Polistes goeldii Ducke, 1904
  • Polistes haugi du Buysson, 1906
  • Polistes hebridensis Giordani Soika, 1981
  • Polistes helveticus Neumeyer, 2014[22]
  • Polistes hirsuticornis Buck, 2012[20]
  • Polistes horrendus Gusenleitner, 2006
  • Polistes huacapistana Richards, 1978
  • Polistes huisunensis Kuo, 1987
  • Polistes humeralis Polašek, 2023
  • Polistes humilis (Fabricius, 1781)
  • Polistes incertus Cresson, 1865
  • Polistes indicus Stolfa, 1934
  • Polistes infuscatus Lepeletier, 1836
  • Polistes instabilis de Saussure, 1853
  • Polistes intermedius Kojima, 1988
  • Polistes iranus Guiglia, 1976
  • Polistes japonicus de Saussure, 1858
  • Polistes jokahamae Radoszkowski, 1887
  • Polistes kaibabensis Hayward, 1932
  • Polistes khasianus Cameron, 1900
  • Polistes laevigatissimus Giordani Soika, 1975
  • Polistes lanio (Fabricius, 1775)
  • Polistes lateritius Smith, 1857
  • Polistes latinis Das & Gupta, 1984
  • Polistes legnotus van der Vecht, 1972
  • Polistes lepcha Cameron, 1900
  • Polistes lineonotus Bohart, 1949
  • Polistes loveridgei Bequaert, 1938
  • Polistes lycus Cameron, 1901
  • Polistes macrocephalus Bequaert, 1918
  • Polistes madecassus de Saussure, 1853
  • Polistes madiburensis von Schulthess, 1921
  • Polistes major Palisot de Beauvois, 1818
  • Polistes mandarinus de Saussure, 1853
  • Polistes maranonensis Willink, 1964
  • Polistes marginalis (Fabricius, 1775)
  • Polistes maroccanus Schmid-Egger, 2017[23]
  • Polistes meadeanus von Schulthess, 1913
  • Polistes melanopterus Cameron, 1911
  • Polistes melanosoma de Saussure, 1853
  • Polistes melanotus Richards, 1978
  • Polistes mertoni du Buysson, 1913
  • Polistes metricus Say, 1831
  • Polistes mexicanus Bequaert, 1940
  • Polistes minor Palisot de Beauvois, 1818
  • Polistes mongolicus Buysson, 1911[23]
  • Polistes moraballi Richards, 1951
  • Polistes myersi Bequaert, 1934
  • Polistes mysteriosus Bequaert, 1938
  • Polistes niger Brèthes, 1903
  • Polistes nigrifrons Smith, 1859
  • Polistes nigritarsis Cameron, 1900
  • Polistes nimpha (Christ, 1791)
  • Polistes ninabamba Richards, 1978
  • Polistes nipponensis Pérez, 1905
  • Polistes notatipes Richards, 1978
  • Polistes obscurus de Saussure, 1863
  • Polistes occipitalis Ducke, 1904
  • Polistes occultus Kojima, 1988
  • Polistes oculatus Smith, 1857
  • Polistes olivaceus (DeGeer, 1773)
  • Polistes opacus Gusenleitner, 2006
  • Polistes ornatus Lepeletier, 1836
  • Polistes pacificus Fabricius, 1804
  • Polistes palmarum Bequaert, 1936
  • Polistes paraguayensis Bertoni, 1921
  • Polistes parametricus Buck, 2012[20]
  • Polistes penai Richards, 1978
  • Polistes penthicus van der Vecht, 1972
  • Polistes perflavus van der Vecht, 1972
  • Polistes peruvianus Bequaert, 1934
  • Polistes philippinensis de Saussure, 1853
  • Polistes poeyi Lepeletier, 1836
  • Polistes praenotatus Kohl, 1908
  • Polistes pseudoculatus Snelling, 1955
  • Polistes quadricingulatus Gusenleitner, 2006
  • Polistes ridleyi Kirby, 1890
  • Polistes riekii Richards, 1978
  • Polistes riparius Yamane & Yamane, 1987
  • Polistes rossi Bohart, 1949
  • Polistes rothneyi Cameron, 1900
  • Polistes rubellus Gusenleitner, 2006
  • Polistes rubiginosus Lepeletier, 1836[20]
  • Polistes rufidens de Saussure, 1853
  • Polistes rufiventris Ducke, 1904
  • Polistes rufodorsalis Yamane & Kusigemati, 1985
  • Polistes sagittarius de Saussure, 1853
  • Polistes santoshae Das & Gupta, 1984
  • Polistes satan Bequaert, 1940
  • Polistes saussurei Dalla Torre, 1894
  • Polistes schach (Fabricius, 1781)
  • Polistes semenowi Morawitz, 1889
  • Polistes semiflavus Holmgren, 1868
  • Polistes sgarambus Giordani Soika, 1975
  • Polistes shirakii Sonan, 1943
  • Polistes sikorae de Saussure, 1900
  • Polistes similis Das & Gupta, 1984
  • Polistes simillimus Zikán, 1951
  • Polistes simulatus Smith, 1860
  • Polistes smithii de Saussure, 1853
  • Polistes snelleni de Saussure, 1862
  • Polistes stabilinus Richards, 1978
  • Polistes stenopus van der Vecht, 1972
  • Polistes stigma (Fabricius, 1793)
  • Polistes strigosus Bequaert, 1940
  • Polistes subsericeus de Saussure, 1854
  • Polistes takasagonus Sonan, 1943
  • Polistes tenebricosus Lepeletier, 1836
  • Polistes tenebris Nguyen & Lee 2017[24]
  • Polistes tenellus du Buysson, 1905
  • Polistes tenuispunctia Kim, 2001
  • Polistes tepidus (Fabricius, 1775)
  • Polistes testaceicolor Bequaert, 1937
  • Polistes thoracicus Fox, 1898
  • Polistes torresae Silveira, 1994
  • Polistes tristis Meade-Waldo, 1911
  • Polistes tullgreni Schulz, 1906
  • Polistes utakwae Meade-Waldo, 1916
  • Polistes variabilis (Fabricius, 1781)
  • Polistes veracrucis Richards, 1978
  • Polistes versicolor (Olivier, 1792)
  • Polistes wattii Cameron, 1900
  • Polistes watutus Kojima, 1988
  • Polistes weyrauchorum Willink, 1964
  • Polistes williamsi Petersen, 1990
  • Polistes xanthogaster Bequaert, 1940
  • Polistes xantholeucus van der Vecht, 1984
  • Pest status[edit]

    Polistes chinensis antennalis, Asian paper wasp has established itself as a pest species in New Zealand.

    Along with the German and common wasps, the Asian and Australian paper wasps (P. chinensis and P. humilis) are considered pests in New Zealand. Arriving in 1979,[26] the Asian paper wasp has established itself in both the North Island and the northern parts of the South Island. Because it competes with native species (such as the kaka) for insects, nectar, and honeydew,[27][28] it is a hindrance to conservation efforts.[citation needed]

    InNorth America, the introduced European species Polistes dominula has rapidly colonized a significant area, and is considered an invasive pest.[29][30] It is a concern for cherry and grape growers in British Columbia, as it injures the fruit by biting off the skin. It also spreads yeast and fungi that harm fruit and can be a nuisance to workers and pickers at harvest.[31] There is evidence it has also displaced native paper wasp species by outcompeting them.[32]

    Parasites[edit]

    Various other insects are parasitesorparasitoidsofPolistes, including flies (e.g., Sarcophagidae), mantispids, and wasps in the families Torymidae, Mutillidae (rarely), Braconidae, and Ichneumonidae (e.g. Latibulus argiolus). Some more specialized groups are more intimately associated with Polistes; this includes strepsipterans in the family Stylopidae (genus Xenos), wasps of the genus Elasmus (formerly placed in their own family, "Elasmidae"), and wasps in the family Trigonalidae.

    The nests of many species of this wasp genus are invaded by the parasitoid caterpillars of the moth Chalcoela iphitalis which feed on the wasp larvae and pupas at night, spinning their cocoons in empty cells.[33][34][35]

    Within the subgenus Polistes are four known social obligate parasites: P. atrimandibularis, P. austroccidentalis, P. maroccanus, and P. semenowi, which parasitize other Polistes wasps.[23] Known host species of these parasites are P. dominulus, P. gallicus, P. nimphus, P. associus, and P. biglumis.[36] Although these parasites differ in their host invasion strategies, their end goal is to successfully infiltrate the host nest and reproduce at the host's expense.[citation needed]

    References[edit]

    1. ^ Carpenter, James M. (2008). "Review of Hawaiian Vespidae (Hymenoptera)" (PDF). Occasional Papers of the Bishop Museum. 99: 1–18. Archived from the original (PDF) on 6 September 2017.
  • ^ a b "Polistes Latreille, 1802". Fauna Europaea. Fauna Europaea Secretariat, Museum für Naturkunde Leibniz & Institut für Evolutions- und Biodiversitätsforschung. Retrieved 22 January 2020.
  • ^ a b Ebeling, Walter (1975). "Chapter 9, part 2: Pests Attacking Man and his Pets". Urban Entomology. Berkeley: Division of Agricultural Sciences, University of California (UC Riverside Entomology). ISBN 978-0931876196.
  • ^ Chakraborti, Suktara (2018). "Linking insect diversity with habitat health at the ecologically restored sites of the Lokkere Reserve Forest, Bandipur Tiger Reserve, Karnataka". JungleScapes (JS-Insects-001). doi:10.13140/RG.2.2.25359.02721.
  • ^ a b Carpenter, James M. (1996). "Distributional Checklist of Species of the Genus Polistes (Hymenoptera: Vespidae; Polistinae, Polistini)". American Museum Novitates (3188): 1–39. Retrieved 24 September 2023.
  • ^ a b Buck, M.; Marshall, S. A.; Cheung, D. K. B. (2008). "Identification Atlas of the Vespidae (Hymenoptera, Aculeata) of the northeastern Nearctic region". Canadian Journal of Arthropod Identification. 05: 1–492. doi:10.3752/cjai.2008.05.
  • ^ Dani, Francesca Romana (2006). "Cuticular lipids as semiochemicals in paper wasps and other social insects". Annales Zoologici Fennici. 43 (5/6). Finnish Zoological and Botanical Publishing Board + Ministry of Education and Culture: 500–514. ISSN 0003-455X. JSTOR 23736758. ISSN 1797-2450.
  • ^ a b Reeve, Hudson K. (1991). "Polistes". In Kenneth G. Ross; Robert W. Mathew (eds.). The Social Biology of Wasps. Cornell University Press. pp. 99–148. ISBN 978-0-8014-9906-7.
  • ^ Hamilton, W. D. (1964). "The genetical evolution of social behaviour, I & II". Journal of Theoretical Biology. 7 (1): 17–52. Bibcode:1964JThBi...7...17H. doi:10.1016/0022-5193(64)90039-6. PMID 5875340.
  • ^ West-Eberhard, Mary Jane (10 April 2003). Developmental Plasticity and Evolution. Oxford University Press. p. 447. ISBN 978-0-19-512235-0.
  • ^ Clapperton, B. Kay; Lo, Peter (April 2005). "Nesting biology of Asian paper wasps Polistes chinensis antennalis Pérez, and Australian paper wasps P. humilis (Fab.) (Hymenoptera: Vespidae) in northern New Zealand". New Zealand Journal of Zoology. 27 (3): 189. doi:10.1080/03014223.2000.9518225.
  • ^ West-Eberhard, Mary Jane (1986). "Dominance Relations in Polistes canadensis (L.), a Tropical Social Wasp". Monitore Zoologico Italiano. 20: 263–281. doi:10.1080/00269786.1986.10736502 (inactive 31 January 2024).{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)
  • ^ Hughes, Colin R.; Queller, David C.; Strassman, Joan E.; Davis, Scott K. (1993). "Relatedness and altruism in Polistes wasps". Behavioral Ecology. 4 (2): 128–137. doi:10.1093/beheco/4.2.128.
  • ^ Jandt, J.M.; Tibbetts, E.A.; Toth, A.L. (2013). "Polistes paper wasps: a model genus for the study of social dominance hierarchies". International Journal for the Study of Social Arthropods. 61: 11–27. doi:10.1007/s00040-013-0328-0. S2CID 253637849.
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  • ^ Singer, T.L.; Espelie, K.E. (1 August 1997). "Exposure to nest paper hydrocarbons is important for nest recognition by a social wasp, Polistes metricus Say (Hymenoptera, Vespidae)". Insectes Sociaux. 44 (3): 245–254. doi:10.1007/s000400050045. ISSN 1420-9098.
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  • Further reading[edit]

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