Temporal range: Early Cretaceous – Recent, 100–0 Ma
|The sugarbag bee, Tetragonula carbonaria|
Bees are flying insects closely related to wasps and ants, known for their role in pollination and, in the case of the best-known bee species, the European honey bee, for producing honey and beeswax. Bees are a monophyletic lineage within the superfamily Apoidea, presently considered as a clade Anthophila. There are nearly 20,000 known species of bees in seven to nine recognized families, though many are undescribed and the actual number is probably higher. They are found on every continent except Antarctica, in every habitat on the planet that contains insect-pollinated flowering plants.
Some species including honey bees, bumblebees, and stingless bees live socially in colonies. Bees are adapted for feeding on nectar and pollen, the former primarily as an energy source and the latter primarily for protein and other nutrients. Most pollen is used as food for larvae. Bee pollination is important both ecologically and commercially; the decline in wild bees has increased the value of pollination by commercially managed hives of honey bees.
Bees range in size from tiny stingless bee species whose workers are less than 2 millimetres (0.08 in) long, to Megachile pluto, the largest species of leafcutter bee, whose females can attain a length of 39 millimetres (1.54 in). The most common bees in the Northern Hemisphere are the Halictidae, or sweat bees, but they are small and often mistaken for wasps or flies. Vertebrate predators of bees include birds such as bee-eaters; insect predators include beewolves and dragonflies.
Human beekeeping or apiculture has been practised for millennia, since at least the times of Ancient Egypt and Ancient Greece. Apart from honey and pollination, honey bees produce beeswax, royal jelly and propolis. Bees have appeared in mythology and folklore, again since ancient times, and they feature in works of literature as varied as Beatrix Potter's The Tale of Mrs Tittlemouse, W. B. Yeats's poem The Lake Isle of Innisfree, and Laline Paull's The Bees. Bee larvae are included in the Javanese dish botok tawon, where they are eaten steamed with shredded coconut.
- 1 Evolution
- 2 Description
- 3 Sociality
- 4 Biology
- 5 Ecology
- 6 Bees and humans
- 7 See also
- 8 Notes
- 9 References
- 10 Sources
- 11 External links
The ancestors of bees were wasps in the family Crabronidae, which were predators of other insects. The switch from insect prey to pollen may have resulted from the consumption of prey insects which were flower visitors and were partially covered with pollen when they were fed to the wasp larvae. This same evolutionary scenario may have occurred within the vespoid wasps, where the pollen wasps evolved from predatory ancestors. Until recently, the oldest non-compression bee fossil had been found in New Jersey amber, Cretotrigona prisca of Cretaceous age, a corbiculate bee. A bee fossil from the early Cretaceous (~100 mya), Melittosphex burmensis, is considered "an extinct lineage of pollen-collecting Apoidea sister to the modern bees". Derived features of its morphology (apomorphies) place it clearly within the bees, but it retains two unmodified ancestral traits (plesiomorphies) of the legs (two mid-tibial spurs, and a slender hind basitarsus), showing its transitional status. By the Eocene (~45 mya) there was already considerable diversity among eusocial bee lineages.[a]
The highly eusocial corbiculate Apidae appeared roughly 87 Mya, and the Allodapini (within the Apidae) around 53 Mya. The Colletidae appear as fossils only from the late Oligocene (~25 Mya) to early Miocene. The Melittidae are known from Palaeomacropis eocenicus in the Early Eocene. The Megachilidae are known from trace fossils (characteristic leaf cuttings) from the Middle Eocene. The Andrenidae are known from the Eocene-Oligocene boundary, around 34 Mya, of the Florissant shale. The Halictidae first appear in the Early Eocene with species  found in amber. The Stenotritidae are known from fossil brood cells of Pleistocene age.
The earliest animal-pollinated flowers were shallow, cup-shaped blooms pollinated by insects such as beetles, so the syndrome of insect pollination was well established before the first appearance of bees. The novelty is that bees are specialized as pollination agents, with behavioral and physical modifications that specifically enhance pollination, and are the most efficient pollinating insects. In a process of coevolution, flowers developed longer tubes and bees developed longer tongues to extract the nectar. This drove the adaptive radiation of the angiosperms, and, in turn, the bees themselves.
This cladogram is based on Debevic et al. 2012, which used molecular phylogeny to demonstrate that the bees arose from deep within the Crabronidae, which is therefore paraphyletic. The Heterogynaidae is also broken up. 
This cladogram of the bee families is based on Gullan and Cranston, 2014.[b] They note the "Melittidae" (sensu lato) as paraphyletic but do not resolve it into its separate families. The cladogram uses Danforth et al., 2006, and Michez, 2007 for this purpose. English names, where available, are given in parentheses.
It is usually easy to recognise that a particular insect is a bee. They differ from closely related groups such as wasps by having branched or plume-like setae (bristles), combs on the forelimbs for cleaning their antennae, small anatomical differences in the limb structure and the venation of the hind wings, and in females, by having the seventh dorsal abdominal plate divided into two half-plates.
Behaviourally, one of the most obvious characteristics of bees is that they collect pollen to provide provisions for their young, and have the necessary adaptations to do this. However, certain wasp species such as pollen wasps have similar behaviours, and a few species of bee scavenge from carcases to feed their offspring. The world's largest species of bee is thought to be the Indonesian resin bee Megachile pluto, whose females can attain a length of 39 millimetres (1.54 in). The smallest species may be dwarf stingless bees in the tribe Meliponini whose workers are less than 2 millimetres (0.08 in) in length.
A bee has a pair of large compound eyes which cover much of the surface of the head. Between and above these are three small simple eyes (ocelli) which provide information for the bee on light intensity. The antennae usually have thirteen segments in males and twelve in females and are geniculate, having an elbow joint part way along. They house large numbers of sense organs that can detect touch (mechanoreceptors), smell and taste, and small, hairlike mechanoreceptors that can detect air movement so as to "hear" sounds. The mouthparts are adapted for both chewing and sucking by having both a pair of mandibles and a long proboscis for sucking up nectar.
The thorax has three segments, each with a pair of robust legs, and a pair of membranous wings on the hind two segments. The front legs of corbiculate bees bear combs for cleaning the antennae, and in many species the hind legs bear pollen baskets, flattened sections with incurving hairs to secure the collected pollen. The wings are synchronised in flight and the somewhat smaller hind wings connect to the forewings by a row of hooks along their margin which connect to a groove in the forewing. The abdomen has nine segments, the hindermost three being modified into the sting.
Haplodiploid breeding system
According to inclusive fitness theory, organisms can gain fitness not just through increasing their own reproductive output, but also that of close relatives. In evolutionary terms, individuals should help relatives when Cost < Relatedness * Benefit. The requirements for eusociality are more easily fulfilled by haplodiploid species such as bees because of their unusual relatedness structure. In haplodiploid species, females develop from fertilized eggs and males from unfertilized eggs. Because a male is haploid (has only one copy of each gene), his daughters (which are diploid, with two copies of each gene) share 100% of his genes and 50% of their mother's. Therefore, they share 75% of their genes with each other. This mechanism of sex determination gives rise to what W. D. Hamilton termed "supersisters", more closely related to their sisters than they would be to their own offspring. Workers often do not reproduce, but they can pass on more of their genes by helping to raise their sisters (as queens) than they would by having their own offspring (each of which would only have 50% of their genes). This unusual situation has been proposed as an explanation of the multiple independent evolutions of eusociality (arising at least nine separate times) within the Hymenoptera. However, some eusocial species such as termites are not haplodiploid. Conversely, many bees are haplodiploid yet are not eusocial, and among eusocial species many queens mate with multiple males, creating half-sisters that share only 25% of their genes. Haplodiploidy is thus neither necessary nor sufficient for eusociality. But, monogamy (queens mating singly) is the ancestral state for all eusocial species so far investigated, so it is likely that haplodiploidy contributed to the evolution of eusociality in bees.
Bees may be solitary or may live in various types of communities. The most advanced of these are eusocial colonies found among the honey bees, bumblebees, and stingless bees; these are characterised by having cooperative brood care and a division of labour into reproductive and non-reproductive adults. Sociality, of several different types, is believed to have evolved separately many times within the bees. In some species, groups of cohabiting females may be sisters, and if there is a division of labour within the group, they are considered semisocial. The group is called eusocial if, in addition, the group consists of a mother (the queen) and her daughters (workers), with male drones at certain stages. When the castes are purely behavioural alternatives, the system is considered primitively eusocial as in many paper wasps; when the castes are morphologically discrete, the system is considered highly eusocial.
There are many more species of primitively eusocial than highly eusocial bees, but they have rarely been studied. Most are in the family Halictidae, or "sweat bees". Colonies are typically small, with a dozen or fewer workers, on average. Queens and workers differ only in size, if at all. Most species have a single season colony cycle, even in the tropics, and only mated females hibernate. A few species have long active seasons and attain colony sizes in the hundreds. The orchid bees include some primitively eusocial species with similar biology. Some allodapine bees are primitively eusocial colonies, with progressive provisioning: a larva's food is supplied gradually as it develops, as is the case in honey bees and some bumblebees.
Bumblebees are eusocial, like the eusocial Vespidae such as hornets. The queen initiates a nest on her own. Bumblebee colonies typically have from 50 to 200 bees at peak population, which occurs in mid to late summer. Nest architecture is simple, limited by the size of the pre-existing nest cavity, and colonies rarely last more than a year. In 2011, the International Union for Conservation of Nature set up the Bumblebee Specialist Group to review the threat status of all bumblebee species world-wide using the IUCN Red List criteria.
The true honey bees (genus Apis) are highly eusocial, and are among the best known of all insects. There are 29 subspecies of Apis mellifera, native to Europe, the Middle East, and Africa. Africanized bees are a hybrid strain of A. mellifera that escaped from experiments involving crossing European and African subspecies; they are unusually defensive.
Solitary and communal bees
Most other bees, including familiar insects such as carpenter bees, leafcutter bees and mason bees are solitary in the sense that every female is fertile, and typically inhabits a nest she constructs herself. There are no worker bees for these species. Solitary bees typically produce neither honey nor beeswax.
Solitary bees are important pollinators; they gather pollen to provision their nests with food for their brood. Often it is mixed with nectar to form a paste-like consistency. Some solitary bees have advanced types of pollen-carrying structures on their bodies. A very few species of solitary bees are being cultured for commercial pollination. Most of these species belong to a distinct set of genera, namely: carpenter bees, sweat bees, mason bees, polyester bees, squash bees, dwarf carpenter bees, leafcutter bees, alkali bees and digger bees.
Solitary bees are often oligoleges, in that they only gather pollen from one or a few species or genera of closely related plants (unlike honey bees and bumblebees which are generalists). Specialist pollinators also include bee species which gather floral oils instead of pollen, and male orchid bees, which gather aromatic compounds from orchids (one of the few cases where male bees are effective pollinators). The bees are often drawn to their specialist flower by the odour of the pollen defence chemicals created by the plant. In a very few cases only one species of bee can effectively pollinate a single plant species, and some plants are endangered at least in part because their pollinator is also threatened. There is, however, a pronounced tendency for oligolectic bees to be associated with common, widespread plants which are visited by multiple pollinators. There are some forty oligoleges associated with the creosote bush in the arid parts of the United States southwest, for example.
Solitary bees create nests in hollow reeds or twigs, holes in wood, or, most commonly, in tunnels in the ground. The female typically creates a compartment (a "cell") with an egg and some provisions for the resulting larva, then seals it off. A nest may consist of numerous cells. When the nest is in wood, usually the last (those closer to the entrance) contain eggs that will become males. The adult does not provide care for the brood once the egg is laid, and usually dies after making one or more nests. The males typically emerge first and are ready for mating when the females emerge. Solitary bees are either stingless or very unlikely to sting (only in self-defense, if ever).
While solitary females each make individual nests, some species are gregarious, preferring to make nests near others of the same species, and giving the appearance of being social. Large groups of solitary bee nests are called aggregations, to distinguish them from colonies. In some species, multiple females share a common nest, but each makes and provisions her own cells independently. This type of group is called "communal" and is not uncommon. The primary advantage appears to be that a nest entrance is easier to defend from predators and parasites when there are multiple females using that same entrance on a regular basis.
The life cycle of a bee, be it a solitary or social species, involves the laying of an egg, the development through several moults of a legless larva, a pupation stage during which the insect undergoes complete metamorphosis, followed by the emergence of a winged adult. Most solitary bees and bumble bees in temperate climates overwinter as adults or pupae and emerge in spring when increasing numbers of flowering plants come into bloom. The males usually emerge first and search for females with which to mate. The sex of a bee is determined by whether or not the egg is fertilised; after mating, a female stores the sperm, and determines which sex is required at the time each individual egg is laid, fertilised eggs producing female offspring and unfertilised eggs, males. Tropical bees may have several generations in a year and no diapause stage.
The egg is generally oblong, slightly curved and tapering at one end. In the case of solitary bees, each one is laid in a cell with a supply of mixed pollen and nectar next to it. This may be rolled into a pellet or placed in a pile and is known as mass provisioning. In social species of bee there is progressive provisioning with the larva being fed regularly while it grows. The nest varies from a hole in the ground or in wood, in solitary bees, to a substantial structure with wax combs in bumblebees and honey bees.
The larvae are generally whitish grubs, roughly oval and bluntly-pointed at both ends. They have fifteen segments and spiracles in each segment for breathing. They have no legs but are able to move within the confines of the cell, helped by tubercles on their sides. They have short horns on the head, jaws for chewing their food and an appendage on either side of the mouth tipped with a bristle. There is a gland under the mouth that secretes a viscous liquid which solidifies into the silk they use to produce their cocoons. The pupa can be seen through the semi-transparent cocoon and over the course of a few days, the insect undergoes metamorphosis into the form of the adult bee. When ready to emerge, it splits its skin dorsally and climbs out of the exuviae as a winged adult and breaks out of the cell.
In Antoine Magnan's 1934 book Le vol des insectes, he wrote that he and André Sainte-Laguë had applied the equations of air resistance to insects and found that their flight could not be explained by fixed-wing calculations, but that "One shouldn't be surprised that the results of the calculations don't square with reality". This has led to a common misconception that bees "violate aerodynamic theory", but in fact it merely confirms that bees do not engage in fixed-wing flight, and that their flight is explained by other mechanics, such as those used by helicopters. In 1996 it was shown that vortices created by many insects' wings helped to provide lift. High-speed cinematography and robotic mock-up of a bee wing showed that lift was generated by "the unconventional combination of short, choppy wing strokes, a rapid rotation of the wing as it flops over and reverses direction, and a very fast wing-beat frequency". Wing-beat frequency normally increases as size decreases, but as the bee's wing beat covers such a small arc, it flaps approximately 230 times per second, faster than a fruitfly (200 times per second) which is 80 times smaller.
The ethologist Karl von Frisch studied navigation in the honey bee. He showed that honey bees communicate by the waggle dance, in which a worker indicates the location of a food source to other workers in the hive. He demonstrated that bees can recognize a desired compass direction in three different ways: by the sun, by the polarization pattern of the blue sky, and by the earth’s magnetic field. He showed that the sun is the preferred or main compass; the other mechanisms are used under cloudy skies or inside a dark beehive. Bees navigate using spatial memory with a "rich, map-like organization".
As mimics and models
Many bees are aposematically coloured, typically orange and black, warning of their ability to defend themselves with a powerful sting. As such they are models for Batesian mimicry by non-stinging insects such as bee-flies, robber flies and hoverflies, all of which gain a measure of protection by superficially looking and behaving like bees.
Bees are themselves Müllerian mimics of other aposematic insects with the same colour scheme, including wasps, lycid and other beetles, and many butterflies and moths (Lepidoptera) which are themselves distasteful, often through acquiring bitter and poisonous chemicals from their plant food. All the Müllerian mimics, including bees, benefit from the reduced risk of predation that results from their easily recognised warning coloration.
Bees are also mimicked by plants such as the bee orchid which imitates both the appearance and the scent of a female bee; male bees attempt to mate (pseudocopulation) with the furry lip of the flower, thus pollinating it.
As brood parasites
Brood parasites occur in several bee families including the apid subfamily Nomadinae. Females of these bees lack pollen collecting structures (the scopa) and do not construct their own nests. They typically enter the nests of pollen collecting species, and lay their eggs in cells provisioned by the host bee. When the cuckoo bee larva hatches it consumes the host larva's pollen ball, and often the host egg also.
In the south of Africa, hives of African honeybees (A. mellifera scutellata) are being destroyed by parasitic workers of the Cape honeybee, A. m. capensis. These lay diploid eggs ("thelytoky"), escaping normal worker policing, leading to the colony's destruction; the parasites can then move to other hives.
The cuckoo bees in the Bombus subgenus Psithyrus are closely related to, and resemble, their hosts in looks and size. This common pattern gave rise to the ecological principle "Emery's rule". Others parasitize bees in different families, like Townsendiella, a nomadine apid, two species of which are cleptoparasites of the dasypodaid genus Hesperapis, while the other species in the same genus attacks halictid bees.
Four bee families (Andrenidae, Colletidae, Halictidae, and Apidae) contain some species that are crepuscular. Most are tropical or subtropical, but there are some which live in arid regions at higher latitudes. These bees have greatly enlarged ocelli, which are extremely sensitive to light and dark, though incapable of forming images. Some have refracting superposition compound eyes: these combine the output of many elements of their compound eyes to provide enough light for each retinal photoreceptor. Their ability to fly by night enables them to avoid many predators, and to exploit flowers that produce nectar only or also at night.
Predators, parasites and pathogens
Vertebrate predators of bees include bee-eaters, shrikes and flycatchers, which make short sallies to catch insects in flight. Swifts and swallows fly almost continually, catching insects as they go. The honey buzzard attacks bees' nests and eats the larvae. The greater honeyguide interacts with humans by guiding them to the nests of wild bees. The humans break open the nests and take the honey and the bird feeds on the larvae and the wax. Among mammals, predators such as the badger dig up bumblebee nests and eat both the larvae and any stored food.
Specialist ambush predators of visitors to flowers include crab spiders, which wait on flowering plants for pollinating insects; predatory bugs, and praying mantises, some of which (the flower mantises of the tropics) wait motionless, aggressive mimics camouflaged as flowers. Beewolves are large wasps that habitually attack bees; the ethologist Niko Tinbergen estimated that a single colony of the beewolf Philanthus triangulum might kill several thousand honeybees in a day: all the prey he observed were honeybees. Other predatory insects that sometimes catch bees include robber flies and dragonflies.
Bees and humans
In mythology and folklore
Three bee maidens with the power of divination and thus speaking truth are described in Homer's Hymn to Hermes, and the food of the gods is "identified as honey"; the bee maidens were originally associated with Apollo, and are probably not correctly identified with the Thriae. Honey, according to a Greek myth, was discovered by a nymph called Melissa ("Bee"); and honey was offered to the Greek gods from Mycenean times. Bees were associated, too, with the Delphic oracle and the prophetess was sometimes called a bee.
The image of a community of honey bees has been used from ancient to modern times, in Aristotle and Plato; in Virgil and Seneca; in Erasmus and Shakespeare; Tolstoy, and by political and social theorists such as Bernard Mandeville and Karl Marx as a model for human society. In English folklore, bees would be told of important events in the household, in a custom known as "Telling the bees".
W. B. Yeats's poem The Lake Isle of Innisfree (1888) contains the couplet "Nine bean rows will I have there, a hive for the honey bee, / And live alone in the bee loud glade." At the time he was living in Bedford Park in the West of London.
Sue Monk Kidd's The Secret Life of Bees (2004), and the 2009 film starring Dakota Fanning, tells the story of a girl who escapes her abusive home and finds her way to live with a family of beekeepers, the Boatwrights.
The humorous 2007 animated film Bee Movie used Jerry Seinfeld's first script and was his first work for children; he starred as a bee named Barry B. Benson, alongside Renée Zellweger. Critics found its premise awkward and its delivery tame.
Humans have kept honey bee colonies, commonly in hives, for millennia. Beekeepers collect honey, beeswax, propolis, pollen, and royal jelly from hives; bees are also kept to pollinate crops and to produce bees for sale to other beekeepers.
Depictions of humans collecting honey from wild bees date to 15,000 years ago; efforts to domesticate them are shown in Egyptian art around 4,500 years ago. Simple hives and smoke were used; jars of honey were found in the tombs of pharaohs such as Tutankhamun. From the 18th century, European understanding of the colonies and biology of bees allowed the construction of the moveable comb hive so that honey could be harvested without destroying the colony. Among Classical Era authors, beekeeping with the use of smoke is described in the History of Animals Book 9 (a book not written by Aristotle himself). The account mentions that bees die after stinging; that workers remove corpses from the hive, and guard it; castes including workers and non-working drones, but "kings" rather than queens; predators including toads and bee-eaters; and the waggle dance, with the "irresistible suggestion" of άpοσειονται (aroseiontai, it waggles) and παρακολουθούσιν (parakolouthousin, they watch).[c]
As commercial pollinators
Bees play an important role in pollinating flowering plants, and are the major type of pollinator in many ecosystems that contain flowering plants. It is estimated that one third of the human food supply depends on pollination by insects, birds and bats, most of which is accomplished by bees, especially the domesticated European honey bee.
Contract pollination has overtaken the role of honey production for beekeepers in many countries. From 1972 to 2006, feral honey bees declined dramatically in the US, and they are now almost absent. The number of colonies kept by beekeepers declined slightly, through urbanization, systematic pesticide use, tracheal and Varroa mites, and the closure of beekeeping businesses. In 2006 and 2007 the rate of attrition increased, and was described as colony collapse disorder. In 2010 invertebrate iridescent virus and the fungus Nosema ceranae were shown to be in every killed colony, and deadly in combination. Winter losses increased to about 1/3. Varroa mites were thought to be responsible for about half the losses.
Apart from colony collapse disorder, losses outside the US have been attributed to causes including pesticide seed dressings, such as Clothianidin, Imidacloprid and Thiamethoxam. From 2013 the European Union restricted some pesticides to stop bee populations from declining further. In 2014 the Intergovernmental Panel on Climate Change report warned that bees faced increased risk of extinction because of global warming.
Honey is a natural product produced by bees and stored for their own use, but its sweetness has always appealed to humans. Before domestication of bees was even attempted, humans were raiding their nests for their honey. Smoke was often used to subdue the bees and such activities are depicted in rock paintings in Spain which have been dated to 15,000 BC. Indigenous people in many countries eat insects, including consuming the larvae and pupae of bees, mostly stingless bees. They also gather "bee brood" (the larvae, pupae and surrounding cells) for consumption. In the Indonesian dish botok tawon from Central and East Java, bee larvae are eaten as a companion to rice, after being mixed with shredded coconut, wrapped in banana leaves, and steamed.
Honey bees are used commercially to produce honey. They also produce some substances used as dietary supplements with possible health benefits, pollen, propolis, and royal jelly, though all of these can also cause allergic reactions.
- Triassic nests in a petrified forest in Arizona, implying that bees evolved much earlier, are now thought to be beetle borings.
- Gullan and Cranston give Hines et al, 2007; Debevec et al, 2012; Danforth et al, 2013; and Johnson et al, 2013 as their sources.
- In D'Arcy Thompson's translation: "At early dawn they make no noise, until some one particular bee makes a buzzing noise two or three times and thereby awakes the rest; hereupon they all fly in a body to work. By and by they return and at first are noisy; ... until at last some one bee flies round about, making a buzzing noise, and apparently calling on the others to go to sleep".
- Danforth BN, Sipes S, Fang J, Brady SG (October 2006). "The history of early bee diversification based on five genes plus morphology". Proc. Natl. Acad. Sci. U.S.A. 103 (41): 15118–23. doi:10.1073/pnas.0604033103. PMC 1586180. PMID 17015826.
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- Engel, Michael S. (2001). "Monophyly and Extensive Extinction of Advanced Eusocial Bees: Insights from an Unexpected Eocene Diversity". PNAS (National Academy of Sciences) 98 (4): 1661–1664. doi:10.1073/pnas.041600198. JSTOR 3054932. PMC 29313. PMID 11172007.
- Buchmann, Stephen L.; Nabhan, Gary Paul (2012). The Forgotten Pollinators. Island Press. pp. 41–42. ISBN 978-1-59726-908-7.
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- Danforth, Bryan; Cardinal, Sophie; Praz, Christophe; Almeida, Eduardo; Michez, Denis (28 August 2012). "The Impact of Molecular Data on Our Understanding of Bee Phylogeny and Evolution". Annual Review of Entomology 58: 57–78. doi:10.1146/annurev-ento-120811-153633. Retrieved 2014-11-16.
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- Michez, Denis; Nel, Andre; Menier, Jean-Jacques; Rasmont, Pierre (2007). "The oldest fossil of a melittid bee (Hymenoptera: Apiformes) from the early Eocene of Oise (France)" (PDF). Zoological Journal of the Linnean Society 150: 701–709.
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- Houston, T.F., 1987: "Fossil brood cells of stenotritid bees (Hymenoptera: Apoidea) from the Pleistocene of South Australia". Transactions of the Royal Society of South Australia, 1111-2: 93–97
- Michener, Charles Duncan (1974). The Social Behavior of the Bees: A Comparative Study. Harvard University Press. pp. 22–78. ISBN 978-0-674-81175-1.
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- Gullan and Cranston, 2014. p.328
- Danforth, Bryan N.; Sipes, Sedonia; Fang, Jennife; Brady, Sean N. (2006). "The history of early bee diversification based on five genes plus morphology". PNAS 103 (41): 15118–15123. doi:10.1073/pnas.0604033103.
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