Vespula
Vespula is a genus of eusocial wasps in the family Vespidae and subfamily Vespinae, commonly known as yellowjackets due to their striking black and yellow coloration. These wasps are characterized by their relatively small size, with workers typically measuring 8–16 mm in length, and their ability to sting repeatedly, as they lack a barbed stinger. The genus comprises approximately 26 species, which are distinguished from their sister genus Dolichovespula by features such as a shorter oculo-malar space and typically subterranean nests constructed from chewed wood fibers forming a paper-like envelope.[1][2][3][4] Native primarily to the Holarctic region, species of Vespula exhibit the highest diversity in northern North America and Eurasia, with 13 species confirmed in North America alone. Some species, such as V. germanica and V. vulgaris, have become invasive pests in temperate regions of the Southern Hemisphere, including Australia, New Zealand, and southern South America, where they outcompete native pollinators and scavengers. The genus is divided into informal species groups, including the rufa (or austriaca) group, vulgaris group, and squamosa group, based on morphological and phylogenetic analyses.[2][1][5] Biologically, Vespula species exhibit a typical hymenopteran social structure, with annual colonies initiated by a single fertilized queen in spring who constructs the initial nest and rears the first brood of workers. Workers forage for carbohydrates (e.g., nectar, fruit) and proteins (e.g., insects, carrion), feeding larvae meat while adults consume sugars, making them effective predators of pest insects but also opportunistic scavengers around human food sources. Nests, often located underground in abandoned rodent burrows or cavities, can grow to house thousands of individuals by late summer, producing new queens and males before the colony dies in autumn. Their aggressive defense, triggered by alarm pheromones, contributes to their notoriety, though they play a beneficial role in ecosystems as pollinators and biological control agents.[4][6][2] Human interactions with Vespula often center on their pest status, as foraging workers are attracted to picnics and garbage, leading to stings that cause pain, swelling, and occasionally severe allergic reactions. Notable species include V. pensylvanica (western yellowjacket), common in western North America and highly aggressive, and V. maculifrons (eastern yellowjacket), widespread in the eastern U.S. Management strategies focus on early-season trapping of queens and avoiding attractants, rather than broad insecticides, to minimize environmental impact. Despite these conflicts, their predatory habits help control agricultural pests, highlighting their ecological value.[6][4][7]Taxonomy and Phylogeny
Classification
Vespula is a genus of social wasps belonging to the order Hymenoptera, family Vespidae, and subfamily Vespinae.[3] The genus encompasses ground-nesting yellowjackets, distinguished from related genera by specific apomorphic traits such as the loss of tyloides on male antennal segments, complete loss of the pronotal carina, and fusion of the aedeagus rods apically in males.[1] The genus Vespula was originally described by Carl Gustav Thomson in 1869 as a subgenus of Vespa, with the type species designated as Vespa austriaca Panzer, 1799, by William H. Ashmead in 1902.[1] Nomenclaturally, Vespula has a complex history involving numerous synonyms for its species and subgenera.[3] Various subgenera are recognized in modern classifications, including Vespula sensu stricto (true yellowjackets with subterranean nests), Paravespula (including invasive species like V. germanica), and Rugovespula (primarily Asian species), based on morphological and molecular phylogenetic analyses.[1][8] Dolichovespula, comprising aerial-nesting yellowjackets, was historically debated as a subgenus of Vespula but is now recognized as a distinct sister genus within Vespinae, supported by shared derived characters like the reduction of the scutallamella and twisted pedicel in embryo nests.[1] For genus-level identification, Vespula species exhibit workers with body lengths typically ranging from 8 to 16 mm, prominent yellow and black banding on the abdomen and thorax, and characteristic wing venation including three submarginal cells.[9] These traits, combined with the petiolate abdomen and lack of arolia on pretarsal claws, aid in distinguishing Vespula from confamilial genera like Vespa.[1]Evolutionary History
The genus Vespula traces its origins to the late Eocene, with the earliest known fossil evidence consisting of Vespula? hassiaca, a well-preserved specimen from the Messel Pit in Germany dating to approximately 47 million years ago.[10] This amber-like compression fossil exhibits morphological features, such as wing venation and body proportions, suggestive of early vespine wasps, indicating that Vespula-like forms had already diversified within the subfamily Vespinae by the middle of the Cenozoic era.[11] Subsequent fossil records from Eocene and Oligocene deposits further document the gradual emergence of social vespids, though direct Vespula fossils remain sparse compared to other vespine genera.[12] Phylogenetically, Vespula is positioned within the subfamily Vespinae, forming a close sister group to Dolichovespula, with molecular analyses of mitochondrial DNA supporting the monophyly of these two genera combined as the yellowjacket clade.[13] Genetic studies utilizing restriction fragment length polymorphisms of mtDNA from European species confirm this relationship, showing greater intraspecific similarity than intergeneric divergence and placing Vespula as a derived lineage within Vespinae that diverged around 25–42 million years ago during the Oligocene-Miocene transition.[14] While some phylogenomic datasets challenge the strict monophyly by suggesting Dolichovespula aligns more closely with Vespa, the consensus from mtDNA and multi-locus analyses upholds the traditional grouping, highlighting Vespula's role in the rapid radiation of eusocial vespines.[15] A pivotal evolutionary adaptation in Vespula is the shift from solitary ancestral behaviors to advanced eusociality, characterized by cooperative brood care, division of labor, and overlapping generations, which originated once within the Polistinae + Vespinae clade during the early Paleogene.[16] This transition likely enhanced colony defense and resource efficiency, enabling Vespula species to exploit temperate niches. Complementing this social complexity is the development of striking yellow-and-black aposematic coloration, which serves as a warning signal to predators of the wasps' stinging capability and facilitates Müllerian mimicry complexes with other hymenopterans. This patterning, conserved across Vespula species, represents a common aposematic signal in social wasps.[17] Speciation within Vespula has been profoundly influenced by geographic isolation, particularly through vicariance events during climatic oscillations, including post-glacial expansions across the Holarctic realm following the Last Glacial Maximum around 20,000 years ago. This radiation, driven by recolonization from southern refugia into newly available northern habitats, promoted allopatric divergence and the diversification of subgenera like Pterulites and Vespula s.s., resulting in over 20 extant species adapted to varied temperate ecosystems.[18]Physical Characteristics
Morphology
Vespula wasps exhibit the typical hymenopteran body plan, divided into three primary tagmata: the head, thorax, and abdomen. The head is equipped with large compound eyes that provide a wide field of vision, flanked by three simple ocelli arranged in a triangular formation on the vertex for light detection and orientation. Mandibles are robust and toothed, adapted for mastication of solid food and manipulation of nest materials. Antennae are filiform, consisting of 12 segments in females (including scape, pedicel, and 10 flagellomeres) and 13 segments in males, serving primarily for chemoreception to detect pheromones and environmental cues.[19][20] The thorax is compact and supports the locomotory appendages, including two pairs of membranous wings—the forewings larger than the hindwings—and three pairs of jointed legs. The wings are coupled during flight by a row of hook-like structures (hamuli) along the anterior margin of the hindwing, which interlock with a folded margin on the rear of the forewing to enhance aerodynamic efficiency. The legs are structured for versatile movement, with tarsi equipped for walking on varied surfaces and grasping prey items, featuring tibial spurs and claws for secure hold. Pubescence, or fine hairs, covers parts of the thorax and contributes to sensory feedback through mechanoreception.[19][21] The abdomen is petiolate, connected to the thorax by a narrow waist, and displays sexual dimorphism in segment visibility: females, including workers and queens, possess six externally visible terga, while males have seven. In females, the ovipositor is modified into a retractable stinger for defense and prey subdual, absent in males; the stinger is smooth and connected to venom glands.[22] Abdominal pubescence varies but aids in tactile sensing and thermoregulation across the genus. Color patterns on the abdomen, typically alternating black and yellow bands, show minor variations among species but are consistent within the genus.[19][20]Variation Among Species
Vespula species display notable variation in body size, reflecting adaptations to different ecological niches within the genus. Worker wasps typically range from 8 to 16 mm in length, with queens reaching up to 20 mm; for instance, workers of the larger species Vespula germanica measure 12-15 mm, while those of the smaller V. rufa are 10-12 mm in length.[23][24] Queens across species are consistently larger and more robust than workers, often exceeding 17 mm, as seen in V. rufa queens at 17 mm and V. germanica at up to 20 mm, enabling greater egg-laying capacity and overwintering resilience.[24][23] This size disparity underscores the genus's flexibility, where larger species like V. germanica support expansive colonies compared to the more modest nests of smaller ones like V. rufa.[24] Coloration patterns in Vespula are predominantly black and yellow, serving as aposematic warning signals, but interspecific variations provide key diagnostic traits. For example, Vespula squamosa features yellow markings often suffused with orange, particularly in queens, while V. consobrina exhibits distinctive ivory-white markings instead of bright yellow, creating a black-and-ivory appearance.[25][26] Some species incorporate reddish tones, such as V. rufa, which has ferruginous (rusty red) markings on the head and thorax, contrasting with the typical yellow of more common species like V. vulgaris. These color differences aid in species identification and may influence predator deterrence or mate recognition within diverse habitats.[26] Structural variations among Vespula species include subtle differences in facial features, such as clypeus markings, which are crucial for taxonomic distinction. In V. germanica, the female clypeus typically bears three small black spots, whereas V. vulgaris shows a single, anchor- or dagger-shaped black central mark extending to the dorsal margin.[27][28] Antennal structures also vary slightly between sexes across the genus, with males often possessing longer or more curved scapes that facilitate courtship behaviors, though these traits are consistent with the basic hymenopteran body plan. Sexual dimorphism is pronounced in Vespula, with queens larger and more robust than workers or males to support reproductive roles, while males (drones) are similar in size to workers but feature seven abdominal segments compared to the six in females, along with a tapered, often curled abdomen lacking a stinger.[29][27] This dimorphism ensures division of labor, as queens focus on oviposition, workers on foraging and nest maintenance, and males on mating, with the curled male abdomen aiding in copulation.[29]Distribution and Ecology
Geographic Range
The genus Vespula is native to the Holarctic region, encompassing temperate and boreal zones of North America, Europe, and Asia, with the highest diversity in North America where 13 species are confirmed.[30] Species within the genus exhibit widespread distributions across these continents, with many occurring in forested, grassland, and urban landscapes. For instance, V. vulgaris ranges from western Europe eastward to Japan, while V. germanica is distributed across Eurasia from the Mediterranean Basin to temperate Asia.[31][23] Several Vespula species have been introduced beyond their native ranges, particularly V. germanica and V. vulgaris, which have become invasive in southern temperate regions. These wasps arrived in New Zealand in the mid-20th century, with V. germanica first recorded in 1945 and rapidly spreading to both islands by the 1950s; V. vulgaris established populations starting in 1978, impacting local ecosystems. Similar invasions occurred in Australia starting in the late 1950s for both species, as well as in parts of South America, including Argentina (1980s) and Chile (1970s), through human-mediated transport such as shipping.[32][33][34][35][36][37][38] In terms of elevation, Vespula species occupy habitats from sea level to montane zones, with nests and foraging activity documented up to approximately 1,600 meters in some regions, though workers can travel up to 3,000 meters from nests in alpine areas like the European Alps. Biogeographically, the genus traces its origins to the Palearctic realm, with subsequent diversification leading to Nearctic endemics such as V. pensylvanica, as evidenced by phylogenetic analyses and historical distribution patterns. Invasion timelines, including the 1945 New Zealand arrival of V. germanica, highlight rapid dispersal facilitated by global trade, while distribution maps from regional surveys underscore the Holarctic core with expanding introduced frontiers.[23][30]Habitat Preferences
Vespula species primarily inhabit temperate regions across the Northern and Southern Hemispheres, where they thrive in climates characterized by moderate seasonal variations and temperatures that support their social colony dynamics. Optimal foraging activity occurs at air temperatures ranging from 20 to 30°C, enabling workers to efficiently collect resources while minimizing thermoregulatory stress. Below 10°C, activity sharply declines, and extreme heat above 35°C can limit foraging and increase nest ventilation demands to maintain internal brood temperatures around 30-32°C.[39][40][41] Nest site selection in Vespula is driven by the need for protection, humidity, and structural stability, with most species favoring underground burrows in moist soil, often utilizing pre-existing cavities like abandoned rodent holes or mammal tunnels. These subterranean sites provide insulation against temperature fluctuations and predation risks, while allowing easy access to surrounding foraging grounds. Aerial nests in enclosed cavities are uncommon in the genus but occur occasionally in species such as Vespula squamosa, in sites including tree hollows, rock crevices, wall voids in buildings, or under eaves and shrubs, particularly in areas with limited suitable soil.[4][42][43][44] Vespula wasps show a notable association with human-modified landscapes, frequently establishing colonies in urban environments, forest edges, and open meadows, where diverse microhabitats offer proximity to plentiful food resources like small insects and sugary exudates from plants or human refuse. This adaptability to disturbed habitats, including parks and agricultural fields, has facilitated their range expansion in introduced regions, as these areas often provide warmer microclimates and reduced competition compared to dense natural forests.[45][46][42] Seasonal habitat shifts align with Vespula's annual life cycle in temperate zones, with colonies initiating in spring when queens emerge from overwintering diapause in insulated shelters such as leaf litter piles, bark crevices, or shallow soil depressions. Peak activity spans summer and early fall, during which nests expand in stable, resource-rich sites, before declining with cooler autumn temperatures; only inseminated queens survive winter by seeking out these protected overwintering microhabitats to endure low temperatures and moisture.[4][47][44]Life Cycle and Reproduction
Developmental Stages
The life cycle of Vespula wasps consists of four distinct developmental stages: egg, larva, pupa, and adult, with the entire process from egg to adult typically spanning 28–48 days depending on environmental conditions such as temperature and food availability.[48] In the egg stage, the fertilized queen deposits a single egg in each hexagonal cell of the paper comb she constructs in early spring. These tiny, elongated eggs hatch into larvae after 5–8 days.[48] The larval stage follows, lasting 15–22 days across five instars, during which the legless, grub-like larvae grow rapidly within the protected cells. Workers progressively feed the larvae liquids via trophallaxis—mouth-to-mouth exchange of regurgitated fluids rich in carbohydrates—and masticated solid food, primarily protein from captured insects, to support development.[49][50][51] Upon reaching maturity, the fifth-instar larva spins a silken cap over the cell and enters the pupal stage, which endures 7–14 days. During this quiescent period, the pupa undergoes complete metamorphosis, transforming into the winged adult imago while enclosed in the capped cell.[49][51][48] Adult emergence begins with the first workers chewing through the silk caps after approximately 28–48 days from egg laying, enabling them to assume foraging and nest-building duties. Later in the season, males and new queens emerge from larger cells, marking the reproductive phase; the overall annual colony cycle, from queen initiation to decline, spans 8–10 months in temperate regions.[52][48]Mating Behaviors
In Vespula species, mating primarily occurs during nuptial flights in late summer, when virgin queens (gynes) emerge from the colony and participate in aerial swarms with males (drones). These flights facilitate polyandry, with queens typically mating with multiple males—effective mate numbers averaging around 3.7 across the genus, though some individuals may copulate with up to 10 or more—allowing them to store sufficient sperm in their spermatheca for lifelong use without remating.[53][54] Mating often takes place near prominent landmarks or aggregation sites, where males patrol and females are attracted by pheromones, reducing inbreeding risks through wide dispersal.[55][56] Queen production begins earlier in the colony cycle through differential larval feeding, where workers selectively provide larger, well-fed larvae with more protein-rich food, such as masticated insects, compared to worker-destined larvae that receive less nutrition. This nutritional disparity promotes the development of larger, reproductively capable queens, similar to but distinct from the royal jelly mechanism in honey bees, as Vespula larvae rely on trophallactic exchanges rather than a dedicated glandular secretion.[57][58] The resulting queens are physiologically primed for mating and colony founding. Following insemination, mated queens seek solitary overwintering sites, such as hollow logs, soil crevices, or under bark, entering diapause to survive winter as the only colony survivors. In spring, these queens emerge, initiate new nests independently by laying eggs and provisioning initial larvae, and establish annual colonies without assistance.[56][9] Vespula exhibits haplodiploid sex determination, a form of arrhenotokous parthenogenesis where males develop haploid from unfertilized eggs laid by the queen or workers, while diploid females (queens and workers) arise from fertilized eggs; however, thelytokous parthenogenesis (producing diploid females from unfertilized eggs) is rare and not a primary reproductive strategy in the genus.[59][60]Social Behavior
Colony Structure
Vespula species exhibit a eusocial organization characterized by cooperative brood care, overlapping generations, and a reproductive division of labor within their colonies. A typical annual colony is founded by a single fertilized queen in the spring, who initiates nest construction and lays the first eggs. As the colony grows, it consists of one queen, 1,000 to 5,000 sterile female workers, and hundreds of males during the peak season in late summer.[43][61][62] Caste differentiation is pronounced, with the queen primarily dedicated to egg-laying, producing up to 200 eggs per day at peak productivity to sustain colony expansion. Workers, all female but reproductively suppressed, perform essential tasks such as foraging for food, nursing larvae, and maintaining the nest, with their roles shifting based on age and colony needs. Males, produced later in the season, serve solely reproductive functions, mating with queens from other colonies during nuptial flights and contributing no labor to the nest.[52][63] Communication within the colony relies heavily on pheromones to enforce the social hierarchy and coordinate activities. Pheromones secreted from the queen's mandibular glands act as primer signals, inhibiting ovarian development in workers and reinforcing her dominance to prevent worker reproduction. Alarm pheromones, primarily released from the gaster, alert nestmates to threats, prompting defensive behaviors such as stinging attacks.[64][65] Colonies follow an annual cycle, with senescence occurring in the fall as resources dwindle and temperatures drop. The founding queen and workers gradually die off, while new queens and males emerge for mating; fertilized new queens then depart to seek overwintering sites, ensuring the species' persistence into the next season.[52][22]Foraging and Defense
Foraging in Vespula species is primarily conducted by worker wasps, which exhibit opportunistic and generalist behaviors to provision the colony with essential nutrients. Workers actively hunt live arthropods, such as flies (Diptera), ants (Hymenoptera), and caterpillars (Lepidoptera), paralyzing prey with repeated stings before transporting it back to the nest for larval consumption.[66] This carnivorous hunting targets protein-rich sources, comprising a significant portion of the colony's diet, with studies showing that animal prey accounts for approximately 15% of returning foragers in woodland habitats.[66] Scavenging complements hunting, as workers collect carrion, dead insects, and even vertebrate remains when available, enhancing dietary diversity.[67] Carbohydrates form the bulk of adult worker intake, sourced from nectar, fruit juices, honeydew, and increasingly human-derived foods like sugary beverages in urban or late-season environments. In natural settings, such as honeydew woodlands, 68-85% of foragers return with crop loads of sugary liquids, primarily honeydew from aphids, underscoring the predominance of carbohydrate foraging for adult energy needs.[66] Seasonal shifts occur, with early-season reliance on arthropods and nectar giving way to scavenging human food scraps in autumn, particularly in disturbed habitats where natural resources dwindle.[68] Diet composition varies by species and location; for instance, V. vulgaris diets feature higher proportions of Hymenoptera (up to 35%) and Diptera (27%), while V. germanica emphasizes larger orthopterans and spiders.[67] Recruitment to food sources relies on a combination of pheromonal and visual cues rather than long-distance trail pheromones. Foragers deposit odor marks at profitable sites, which guide subsequent workers via olfactory orientation, while visual landmarks and local enhancement—observing conspecifics at the resource—facilitate site location and exploitation. These mechanisms enable rapid colony response to ephemeral resources without the mass recruitment seen in ants.[69] Defense in Vespula colonies centers on aggressive responses to threats, with workers mounting coordinated stinging attacks on intruders. When disturbed, foragers release alarm pheromones from the venom gland, which elicits heightened agitation, wing-fanning, and recruitment of nestmates to the disturbance site.[70] Severe nest disturbances can lead to intensified defensive mobilization and potential colony failure if the nest is destroyed.[71] Territorial behaviors protect foraging areas and the nest, with workers marking food sources using scent deposits to signal ownership and deter competitors. These markings, combined with physical confrontations, defend against intruders like ants, other wasps, or birds, ensuring exclusive access to high-value resources. Such defenses maintain colony efficiency, particularly during peak foraging periods when competition intensifies.[72]Species Diversity
List of Species
The genus Vespula includes approximately 23 valid species, classified into four main species groups based on phylogenetic analysis: the rufa-group (including V. austriaca and V. rufa), the squamosa-group (V. squamosa and allies), the vulgaris-group (V. vulgaris, V. germanica, and others), and the koreensis-group (V. koreensis and related Asian taxa).[1][3] These groups reflect morphological and distributional patterns, with no formal subgenera recognized in modern taxonomy.[3] The following alphabetical list enumerates all recognized species, with authorities, notes on synonyms or taxonomic status, and brief distribution summaries. Some taxa, such as V. shikamai, are treated as subspecies of V. flaviceps in recent revisions, while others like V. inexspectata represent regional endemics.[3]- Vespula acadica (Sladen, 1918): Synonym Vespa rufa var. americana du Buysson, 1905; vulgaris-group; distributed across northern and western North America, from Canada (Yukon to Nova Scotia) to the United States (AK to NC).[3]
- Vespula alascensis Richards, 1951: Vulgaris-group; endemic to Alaska and northwestern North America.[1]
- Vespula arisana (Sonan, 1929): Koreensis-group; endemic to Taiwan.[3]
- Vespula atropilosa (Sladen, 1918): Rufa-group; found in western North America (Canada: BC, AB; U.S.: WA to NM; Mexico: Baja California).[3]
- Vespula austriaca (Panzer, 1799): Rufa-group; synonyms Vespa borealis Smith, 1843 and Vespa arborea Smith, 1849; Holarctic with extensions into Asia (Europe, North America, Russia to Pakistan and China).[3]
- Vespula consobrina (de Saussure, 1854): Vulgaris-group; synonym Vespa scelesta McFarland, 1888; widespread in North America (Canada to GA).[3]
- Vespula flaviceps (Smith, 1870): Koreensis-group; synonyms Vespa japonica de Saussure, 1858; two subspecies recognized, including V. f. shikamai (debated status); Asian distribution (India to Japan and China).[3]
- Vespula flavopilosa Jacobson, 1978: Vulgaris-group; eastern North America (Canada: MB to NS; U.S.: ND to GA).[3]
- Vespula germanica (Fabricius, 1793): Vulgaris-group; synonym Vespa maculata Scopoli, 1763; native to Palaearctic (Europe to Asia), introduced globally (Australia, New Zealand, South America, southern Africa, and parts of North America).[3]
- Vespula inexspectata Eck, 1994: Squamosa-group; regional endemic to central Mexico (Mexico state, Michoacán).[3]
- Vespula intermedia (du Buysson, 1905): Rufa-group; Central Asian distribution (debated validity in some revisions).[1]
- Vespula kingdonwardi Archer, 1981: Koreensis-group; synonym V. hirsuta Lee, 1986; Himalayan and Southeast Asian (China: Xizang; Nepal; Myanmar).[3]
- Vespula koreensis (Radoszkowski, 1887): Koreensis-group; two subspecies; East Asian (India: Sikkim; China; Korea; Russia: Far East).[3]
- Vespula maculifrons (du Buysson, 1905): Vulgaris-group; synonyms Vespa maculifrons Harris, 1853 (nomen nudum) and V. communis var. flavida Sladen, 1918; eastern North America (Canada: MB to NS; U.S.: MT to FL; Mexico: Tamaulipas).[3]
- Vespula nursei Archer, 1981: Koreensis-group; South and East Asian (India: Kashmir; China: Fujian; Philippines: Luzon).[3]
- Vespula orbata (du Buysson, 1902): Koreensis-group; synonym Vespa minuta Dover, 1925; South Asian (India; Nepal; Myanmar).[3]
- Vespula pensylvanica (de Saussure, 1857): Vulgaris-group; synonym Vespa occidentalis Cresson, 1874; western North America (Canada: BC to MB; U.S.: WA to TX; Mexico: Baja California; introduced to Hawaii).[3]
- Vespula rufa (Linnaeus, 1758): Rufa-group; two subspecies; Holarctic and Asian (Europe, North America: AK, VT; Russia to Nepal and Japan).[3]
- Vespula schrenckii (Radoszkowski, 1861): Rufa-group; synonym of V. rufa in some treatments; East Asian (Russia: Far East; debated status).[1]
- Vespula shidai Ishikawa, Yamane & Wagner, 1980: Koreensis-group; subspecies V. s. amamiana Yamane, 1987; East Asian (Japan: Ryukyu Islands).[3]
- Vespula squamosa (Drury, 1773): Squamosa-group; two subspecies; eastern North America (U.S.: WY to FL; Mexico).[1]
- Vespula structor (Smith, 1857): Koreensis-group; South Asian (India; Nepal; Myanmar; China).[1]
- Vespula sulphurea (de Saussure, 1854): Squamosa-group; southwestern North America (U.S.: CA, AZ; Mexico).[1]
- Vespula vidua (de Saussure, 1854): Vulgaris-group; western North America (Canada: YT to BC; U.S.: AK to CO).[1]
- Vespula vulgaris (Linnaeus, 1758): Vulgaris-group; two subspecies; native to Eurasia, introduced to southern hemisphere (Australia, New Zealand, South America).[3]