Template:Short description Template:About Template:Pp Template:Pp-semi-indef Template:Good article Template:Use dmy dates Template:Automatic taxobox
Bees are winged insects closely related to wasps and ants, known for their roles in pollination and, in the case of the best-known bee species, the western honey bee, for producing honey. Bees are a monophyletic lineage within the superfamily Apoidea. They are currently considered a clade, called Anthophila.<ref>Engel, M. S. (2005) Family-group names for bees (Hymenoptera, Apoidea). American Museum Novitates 3476.</ref> There are over 20,000 known species of bees in seven recognized biological families.<ref name="Danforthetal2006">Template:Cite journal</ref><ref name=Michener2000/><ref>Template:Cite journal</ref> Some speciesTemplate:Sndincluding honey bees, bumblebees, and stingless beesTemplate:Sndlive socially in colonies while most species (>90%)Template:Sndincluding mason bees, carpenter bees, leafcutter bees, and sweat beesTemplate:Sndare solitary.
Bees are found on every continent except Antarctica, in every habitat on the planet that contains insect-pollinated flowering plants. 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. Bees range in size from tiny stingless bee species, whose workers are less than Template:Convert long,<ref name=":0">Template:Cite book</ref> to the leafcutter bee Megachile pluto, the largest species of bee, whose females can attain a length of Template:Convert.
Bees feed 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 their larvae. Vertebrate predators of bees include primates and birds such as bee-eaters; insect predators include beewolves and dragonflies.
Bee pollination is important both ecologically and commercially, and the decline in wild bees has increased the value of pollination by commercially managed hives of honey bees. The analysis of 353 wild bee and hoverfly species across Britain from 1980 to 2013 found the insects have been lost from a quarter of the places they inhabited in 1980.<ref>Template:Cite news</ref>
Human beekeeping or apiculture (meliponiculture for stingless bees) has been practiced for millennia, since at least the times of Ancient Egypt and Ancient Greece. Bees have appeared in mythology and folklore, through all phases of art and literature from ancient times to the present day, although primarily focused in the Northern Hemisphere where beekeeping is far more common. In Mesoamerica, the Mayans have practiced large-scale intensive meliponiculture since pre-Columbian times.<ref name=":0" />
EvolutionEdit
The immediate ancestors of bees were stinging 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.<ref name="Cardinal danforth 2011"/>
Based on phylogenetic analysis, bees are thought to have originated during the Early Cretaceous (about 124 million years ago) on the supercontinent of West Gondwana, just prior to its breakup into South America and Africa. The supercontinent is thought to have been a largely xeric environment at this time; modern bee diversity hotspots are also in xeric and seasonal temperate environments, suggesting strong niche conservatism among bees ever since their origins.<ref name=":1">Template:Cite journal</ref>
Genomic analysis indicates that despite only appearing much later in the fossil record, all modern bee families had already diverged from one another by the end of the Cretaceous. The Melittidae, Apidae, and Megachilidae had already evolved on the supercontinent prior to its fragmentation. Further divergences were facilitated by West Gondwana's breakup around 100 million years ago, leading to a deep Africa-South America split within both the Apidae and Megachilidae, the isolation of the Melittidae in Africa, and the origins of the Colletidae, Andrenidae and Halictidae in South America. The rapid radiation of the South American bee families is thought to have followed the concurrent radiation of flowering plants in the same region. Later in the Cretaceous (80 million years ago), colletid bees colonized Australia from South America (with an offshoot lineage evolving into the Stenotritidae), and by the end of the Cretaceous, South American bees had also colonized North America.<ref name=":1" /> The North American fossil taxon Cretotrigona belongs to a group that is no longer found in North America, suggesting that many bee lineages went extinct during the Cretaceous-Paleogene extinction event.<ref name=":1" />
Following the K-Pg extinction, surviving bee lineages continued to spread into the Northern Hemisphere, colonizing Europe from Africa by the Paleocene, and then spreading east to Asia. This was facilitated by the warming climate around the same time, allowing bees to move to higher latitudes following the spread of tropical and subtropical habitats. By the Eocene (~45 mya) there was already considerable diversity among eusocial bee lineages.<ref name="pnas3054932">Template:Cite journal</ref>Template:Efn A second extinction event among bees is thought to have occurred due to rapid climatic cooling around the Eocene-Oligocene boundary, leading to the extinction of some bee lineages such as the tribe Melikertini. Over the Paleogene and Neogene, different bee lineages continued to spread all over the world, and the shifting habitats and connectedness of continents led to the isolation and evolution of many new bee tribes.<ref name=":1" />
FossilsEdit
The oldest non-compression bee fossil is Cretotrigona prisca, a corbiculate bee of Late Cretaceous age (~70 mya) found in New Jersey amber.<ref name="Cardinal danforth 2011">Template:Cite journal</ref> A fossil from the early Cretaceous (~100 mya), Melittosphex burmensis, was initially considered "an extinct lineage of pollen-collecting Apoidea sister to the modern bees",<ref name="Poinar">Template:Cite journal</ref> but subsequent research has rejected the claim that Melittosphex is a bee, or even a member of the superfamily Apoidea to which bees belong, instead treating the lineage as incertae sedis within the Aculeata.<ref name="Allommation">Template:Cite journal</ref>
The Allodapini (within the Apidae) appeared around 53 Mya.<ref name="danforth2012">Template:Cite journal</ref> The Colletidae appear as fossils only from the late Oligocene (~25 Mya) to early Miocene.<ref>Template:Cite journal</ref> The Melittidae are known from Palaeomacropis eocenicus in the Early Eocene.<ref>Template:Cite journal</ref> The Megachilidae are known from trace fossils (characteristic leaf cuttings) from the Middle Eocene.<ref>Template:Cite journal</ref> The Andrenidae are known from the Eocene-Oligocene boundary, around 34 Mya, of the Florissant shale.<ref>Template:Cite journal</ref> The Halictidae first appear in the Early Eocene<ref>Template:Cite journal</ref> with species<ref name="Engel1995">Template:Cite journal</ref><ref name="Engel2000">Template:Cite journal</ref> found in amber. The Stenotritidae are known from fossil brood cells of Pleistocene age.<ref>Template:Cite journal</ref>
CoevolutionEdit
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 floral rewards<ref name="Armbruster ch. 3 Evol. Plant-pollinator relationships">Template:Cite book</ref> such as nectar and longer tubes, and bees developed longer tongues to extract the nectar.<ref name=Michener1974/> Bees also developed structures known as scopal hairs and pollen baskets to collect and carry pollen. The location and type differ among and between groups of bees. Most species have scopal hairs on their hind legs or on the underside of their abdomens. Some species in the family Apidae have pollen baskets on their hind legs, while very few lack these and instead collect pollen in their crops.<ref name=Michener2000>Template:Cite book</ref> The appearance of these structures drove the adaptive radiation of the angiosperms, and, in turn, bees themselves.<ref name=Buchmann2012>Template:Cite book</ref> Bees coevolved not only with flowers but it is believed that some species coevolved with mites. Some provide tufts of hairs called acarinaria that appear to provide lodgings for mites; in return, it is believed that mites eat fungi that attack pollen, so the relationship in this case may be mutualistic.<ref name=":5">Template:Cite journal</ref><ref name="Pavel B 2007">Template:Cite journal</ref>
PhylogenyEdit
ExternalEdit
Molecular phylogeny was used by Debevic et al, 2012, to demonstrate that the bees (Anthophila) arose from deep within the Crabronidae sensu lato, which was thus rendered paraphyletic. In their study, the placement of the monogeneric Heterogynaidae was uncertain. The small family Mellinidae was not included in this analysis.<ref>Template:Cite journal</ref>
Further studies by Sann et al., 2018, elevated the subfamilies (plus one tribe and one subtribe) of Crabronidae sensu lato to family status. They also recovered the placement of Heterogyna within Nyssonini and sunk Heterogynaidae. The newly erected family, Ammoplanidae, formerly a subtribe of Pemphredoninae, was recovered as the most sister family to bees.<ref name=Sann2018>Template:Cite journal</ref>
InternalEdit
This cladogram of the bee families is based on Hedtke et al., 2013, which places the former families Dasypodaidae and Meganomiidae as subfamilies inside the Melittidae.<ref name=Hedtke2013>Template:Cite journal</ref> English names, where available, are given in parentheses.
CharacteristicsEdit
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Bees differ from closely related groups such as wasps by having branched or plume-like setae (hairs), combs on the forelimbs for cleaning their antennae, small anatomical differences in limb structure, and the venation of the hind wings; and in females, by having the seventh dorsal abdominal plate divided into two half-plates.<ref name=Grimaldi>Template:Cite book</ref>
Bees have the following characteristics:<ref name=Extension/>
- 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 on light intensity.<ref name=Extension/>
- The antennae usually have 13 segments in males and 12 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.<ref name=Extension/>
- The mouthparts are adapted for both chewing and sucking by having both a pair of mandibles and a long proboscis for sucking up nectar.<ref name=Extension>{{#invoke:citation/CS1|citation
|CitationClass=web }}</ref>
- 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 synchronized 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.<ref name=Extension/>
The largest species of bee is thought to be Wallace's giant bee Megachile pluto, whose females can attain a length of Template:Convert.<ref>Template:Cite journal</ref> The smallest species may be dwarf stingless bees in the tribe Meliponini whose workers are less than Template:Convert in length.<ref>Template:Cite journal</ref>
SocialityEdit
Haplodiploid breeding systemEdit
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.<ref name=Hughes2008>Template:Cite journal</ref>
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.<ref name="Hamilton1964II">Template:Cite journal</ref> 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), assuming they would produce similar numbers. This unusual situation has been proposed as an explanation of the multiple (at least nine) evolutions of eusociality within Hymenoptera.<ref name="Hughes" /><ref>Template:Cite book</ref>
Haplodiploidy is neither necessary nor sufficient for eusociality. Some eusocial species such as termites are not haplodiploid. Conversely, all bees are haplodiploid but not all are eusocial, and among eusocial species many queens mate with multiple males, creating half-sisters that share only 25% of each other's genes.<ref name="NTW">Template:Cite journal</ref> 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.<ref name="Hughes">Template:Cite journal</ref>
EusocialityEdit
Bees may be solitary or may live in various types of communities. Eusociality appears to have originated from at least three independent origins in halictid bees.<ref>Template:Cite journal</ref> The most advanced of these are species with eusocial colonies; these are characterized by cooperative brood care and a division of labour into reproductive and non-reproductive adults, plus overlapping generations.<ref>Template:Cite book</ref> This division of labour creates specialized groups within eusocial societies which are called castes. 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). When the castes are purely behavioural alternatives, with no morphological differentiation other than size, the system is considered primitively eusocial, as in many paper wasps; when the castes are morphologically discrete, the system is considered highly eusocial.<ref name=Michener1974>Template:Cite book</ref>
True honey bees (genus Apis, of which eight species are currently recognized) are highly eusocial, and are among the best known insects. Their colonies are established by swarms, consisting of a queen and several thousand workers. There are 29 subspecies of one of these species, 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 extremely defensive.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Stingless bees are also highly eusocial. They practice mass provisioning, with complex nest architecture and perennial colonies also established via swarming.<ref name=":0" /><ref>Template:Cite journal</ref>
Many bumblebees are eusocial, similar to the eusocial Vespidae such as hornets in that the queen initiates a nest on her own rather than by swarming. 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.<ref name="BBCT-nest">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> In 2011, the International Union for Conservation of Nature set up the Bumblebee Specialist Group to review the threat status of all bumblebee species worldwide using the IUCN Red List criteria.<ref>Template:Cite news</ref>
There are many more species of primitively eusocial than highly eusocial bees, but they have been studied less often. 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, such as Halictus hesperus.<ref>Template:Cite journal</ref> Some species are eusocial in parts of their range and solitary in others,<ref>Template:Cite journal</ref> or have a mix of eusocial and solitary nests in the same population.<ref>Template:Cite journal</ref> The orchid bees (Apidae) include some primitively eusocial species with similar biology. Some allodapine bees (Apidae) form 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.<ref>Template:Cite book</ref>
Solitary and communal beesEdit
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 is no division of labor so these nests lack queens and worker bees for these species. Solitary bees typically produce neither honey nor beeswax. Bees collect pollen to feed 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.<ref name=Grimaldi/> 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. Very few species of solitary bee are being cultured for commercial pollination. Most of these species belong to a distinct set of genera which are commonly known by their nesting behavior or preferences, namely: carpenter bees, sweat bees, mason bees, plasterer bees, squash bees, dwarf carpenter bees, leafcutter bees, alkali bees and digger bees.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Most solitary bees are fossorial, digging nests in the ground in a variety of soil textures and conditions, while others create nests in hollow reeds or twigs, or holes in wood. 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 very unlikely to sting (only in self-defense, if ever), and some (esp. in the family Andrenidae) are stingless.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
While solitary, females each make individual nests.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Some species, such as the European mason bee Hoplitis anthocopoides,<ref name=Eickwort>Template:Cite journal</ref> and the Dawson's Burrowing bee, Amegilla dawsoni,<ref>Template:Cite journal</ref> 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 multiple females use that same entrance regularly.<ref name=Eickwort/>
BiologyEdit
Life cycleEdit
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. The number of eggs laid by a female during her lifetime can vary from eight or less in some solitary bees, to more than a million in highly social species.<ref>The Bees of the World, Volum 1</ref> 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. Like the other members of Hymenoptera bees are haplodiploid; the sex of a bee is determined by whether or not the egg is fertilized. After mating, a female stores the sperm, and determines which sex is required at the time each individual egg is laid, fertilized eggs producing female offspring and unfertilized eggs, males. Tropical bees may have several generations in a year and no diapause stage.<ref name=Roubik1992>Template:Cite book</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
The egg is generally oblong, slightly curved and tapering at one end. Solitary bees, lay each egg in a separate 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. Social bee species provision progressively, that is, they feed the larva 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.<ref name=Shuckard>Template:Cite book</ref>
In most species, larvae are whitish grubs, roughly oval and bluntly-pointed at both ends. They have 15 segments and spiracles in each segment for breathing. They have no legs but move within the cell, helped by tubercles on their sides. They have short horns on the head, jaws for chewing 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 a cocoon. The cocoon is semi-transparent and the pupa can be seen through it. Over the course of a few days, the larva undergoes metamorphosis into a winged adult. When ready to emerge, the adult splits its skin dorsally and climbs out of the exuviae and breaks out of the cell.<ref name=Shuckard/>
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Nest of common carder bumblebee, wax canopy removed to show winged workers and pupae in irregularly placed wax cells
- Carpenter Bee Galleries.jpeg
Carpenter bee nests in a cedar wood beam (sawn open)
- Bienen mit Brut 2.jpg
Honeybees on brood comb with eggs and larvae in cells
FlightEdit
Antoine Magnan's 1934 book {{#invoke:Lang|lang}} says 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".<ref>Ingram, Jay (2001) The Barmaid's Brain, Aurum Press, pp. 91–92, Template:ISBN.</ref> This has led to a common misconception that bees "violate aerodynamic theory". 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.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> In 1996 it was shown that vortices created by many insects' wings helped to provide lift.<ref>Template:Cite journal</ref> High-speed cinematography<ref>Template:Cite journal</ref> and robotic mock-up of a bee wing<ref name=caltech>{{#invoke:citation/CS1|citation |CitationClass=web }} Re: work of Dr. Michael H. Dickinson.</ref> 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.<ref>Template:Cite journal</ref>
Edit
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.<ref name=vonFrisch93>Template:Cite book</ref> Bees navigate using spatial memory with a "rich, map-like organization".<ref>Template:Cite journal</ref>
DigestionEdit
The gut of bees is relatively simple, but multiple metabolic strategies exist in the gut microbiota.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Pollinating bees consume nectar and pollen, which require different digestion strategies by somewhat specialized bacteria. While nectar is a liquid of mostly monosaccharide sugars and so easily absorbed, pollen contains complex polysaccharides: branching pectin and hemicellulose.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Approximately five groups of bacteria are involved in digestion. Three groups specialize in simple sugars (Snodgrassella and two groups of Lactobacillus), and two other groups in complex sugars (Gilliamella and Bifidobacterium). Digestion of pectin and hemicellulose is dominated by bacterial clades Gilliamella and Bifidobacterium respectively. Bacteria that cannot digest polysaccharides obtain enzymes from their neighbors, and bacteria that lack certain amino acids do the same, creating multiple ecological niches.<ref>Template:Cite journal</ref>
Although most bee species are nectarivorous and palynivorous, some are not. Particularly unusual are vulture bees in the genus Trigona, which consume carrion and wasp brood, turning meat into a honey-like substance.<ref>Template:Cite journal</ref> Drinking guttation drops from leaves is also a source of energy and nutrients.<ref>Plant guttation provides nutrient-rich food for insects - Journals</ref>
EcologyEdit
Floral relationshipsEdit
Most bees are polylectic (generalist) meaning they collect pollen from a range of flowering plants, but some are oligoleges (specialists), in that they only gather pollen from one or a few species or genera of closely related plants.<ref name=Waser2006>Template:Cite book</ref> In Melittidae and Apidae we also find a few genera that are highly specialized for collecting plant oils both in addition to, and instead of, nectar, which is mixed with pollen as larval food.<ref>Template:Cite journal</ref> Male orchid bees in some species gather aromatic compounds from orchids, which is one of the few cases where male bees are effective pollinators. Bees are able to sense the presence of desirable flowers through ultraviolet patterning on flowers, floral odors,<ref name=Dafni>Template:Cite book</ref> and even electromagnetic fields.<ref>Template:Cite journal</ref> Once landed, a bee then uses nectar quality<ref name=Dafni /> and pollen taste<ref>Template:Cite journal</ref> to determine whether to continue visiting similar flowers.
In rare cases, a plant species may only be effectively pollinated by a single bee species, and some plants are endangered at least in part because their pollinator is also threatened. But, there is a pronounced tendency for oligolectic bees to be associated with common, widespread plants visited by multiple pollinator species. For example, the creosote bush in the arid parts of the United States southwest is associated with some 40 oligoleges.<ref>Template:Cite journal</ref>
As mimics and modelsEdit
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Many bees are aposematically colored, 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,<ref name="ThorpHorning1983">Template:Cite book</ref> all of which gain a measure of protection by superficially looking and behaving like bees.<ref name="ThorpHorning1983"/>
Bees are themselves Müllerian mimics of other aposematic insects with the same color 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 recognized warning coloration.<ref>Template:Cite book</ref>
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.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
As brood parasitesEdit
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Brood parasites occur in several bee families including the apid subfamily Nomadinae.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Females of these species 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.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> In particular, the Arctic bee species, Bombus hyperboreus is an aggressive species that attacks and enslaves other bees of the same subgenus. However, unlike many other bee brood parasites, they have pollen baskets and often collect pollen.<ref>Gjershaug, Jan Ove (5 June 2009). "The social parasite bumblebee Bombus hyperboreus Schönherr, 1809 usurp nest of Bombus balteatus Dahlbom, 1832 (Hymenoptera, Apidae) in Norway" (PDF). Norwegian Journal of Entomology 56(1): 28–31. Retrieved 26 September 2015.</ref>
In Southern 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.<ref>Template:Cite book</ref>
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,<ref>Template:Cite journal</ref> while the other species in the same genus attacks halictid bees.<ref>Template:Cite book</ref>
Nocturnal beesEdit
Four bee families (Andrenidae, Colletidae, Halictidae, and Apidae) contain some species that are crepuscular. Most are tropical or subtropical, but some 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.<ref>Template:Cite journal</ref>
Predators, parasites and pathogensEdit
Vertebrate predators of bees include bee-eaters, shrikes and flycatchers, which make short sallies to catch insects in flight.<ref name="ChittkaThomson2001"/> Swifts and swallows<ref name="ChittkaThomson2001"/> fly almost continually, catching insects as they go. The honey buzzard attacks bees' nests and eats the larvae.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> 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.<ref>Template:Cite journal</ref> Among mammals, predators such as the badger dig up bumblebee nests and eat both the larvae and any stored food.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Specialist ambush predators of visitors to flowers include crab spiders, which wait on flowering plants for pollinating insects; predatory bugs, and praying mantises,<ref name="ChittkaThomson2001">Template:Cite book</ref> some of which (the flower mantises of the tropics) wait motionless, aggressive mimics camouflaged as flowers.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Beewolves are large wasps that habitually attack bees;<ref name="ChittkaThomson2001"/> 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.<ref>Template:Cite book</ref> Other predatory insects that sometimes catch bees include robber flies and dragonflies.<ref name="ChittkaThomson2001"/> Honey bees are affected by parasites including tracheal and Varroa mites.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> However, some bees are believed to have a mutualistic relationship with mites.<ref name="Pavel B 2007"/>
Some mites of genus Tarsonemus are associated with bees. They live in bee nests and ride on adult bees for dispersal. They are presumed to feed on fungi, nest materials or pollen. However, the impact they have on bees remains uncertain.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Relationship with humansEdit
In mythology and folkloreEdit
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Homer's Hymn to Hermes describes three bee-maidens with the power of divination and thus speaking truth, and identifies the food of the gods as honey. Sources associated the bee maidens with Apollo and, until the 1980s, scholars followed Gottfried Hermann (1806) in incorrectly identifying the bee-maidens with the Thriae.<ref>Susan Scheinberg, "The Bee Maidens of the Homeric Hymn to Hermes", in Albert Heinrichs, ed., Harvard Studies in Classical Philology (Cambridge MA: Harvard University Press, 1980), 11. Template:ISBN; and many others since questioning Gottfried Hermann's 1806 equation of the Thriae with bee-maidens. Heinrich Gottfried, Homeri nomine dignissimum/Homeric Hymns (Leipzig: 1806), 346 and cxiii. Many took Hermann's unfounded identification at face-value, repeating it ad nauseam, e.g. Hilda M. Ransome, The Sacred Bee in Ancient Times and Folklore (NY: Courier, 1937; reprinted as recently as NY: Dover, 2012), 97. Template:ISBN</ref> 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 also associated with the Delphic oracle and the prophetess was sometimes called a bee.<ref>Template:Cite journal</ref>
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.<ref>Template:Cite book</ref> In English folklore, bees would be told of important events in the household, in a custom known as "Telling the bees".<ref name="Roud2006">Template:Cite book</ref> Honey bees, signifying immortality and resurrection, were royal heraldic emblems of the Merovingians, revived by Napoleon.<ref>Eagle and the bee on the Napoleonic coat of arms</ref>
In art and literatureEdit
Some of the oldest examples of bees in art are rock paintings in Spain which have been dated to 15,000 BC.<ref name=EHSTMNWC>Template:Cite book</ref>
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.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Beatrix Potter's illustrated book The Tale of Mrs Tittlemouse (1910) features Babbity Bumble and her brood (pictured). Kit Williams' treasure hunt book The Bee on the Comb (1984) uses bees and beekeeping as part of its story and puzzle. 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.
Bees have appeared in films such as Jerry Seinfeld's animated Bee Movie,<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> or Eugene Schlusser's A Sting in the Tale (2014). The playwright Laline Paull's fantasy The Bees (2015) tells the tale of a hive bee named Flora 717 from hatching onwards.<ref>Template:Cite news</ref>
BeekeepingEdit
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Humans have kept honey bee colonies, commonly in hives, for millennia.<ref name=Aristotle/> 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.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Simple hives and smoke were used.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref name="Bodenheimer1960">Template:Cite book</ref>
Among Classical Era authors, beekeeping with the use of smoke is described in Aristotle's History of Animals Book 9.<ref name=Aristotle>Template:Cite book</ref> 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 {{#invoke:Lang|lang}} ("{{#invoke:Lang|lang}}", it waggles) and {{#invoke:Lang|lang}} ("{{#invoke:Lang|lang}}", they watch).<ref name=Whitfield>Template:Cite journal</ref>Template:Efn Beekeeping is described in detail by Virgil in his Georgics; it is mentioned in his Aeneid, and in Pliny's Natural History.<ref name=Whitfield/>
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.<ref>Thomas Wildman, A Treatise on the Management of Bees (London, 1768, 2nd edn 1770).</ref><ref>Template:Cite journal</ref>
As commercial pollinatorsEdit
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, whether wild or domesticated.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>Template:Cite news</ref>
Since the 1970s, there has been a general decline in the species richness of wild bees and other pollinators, probably attributable to stress from increased parasites and disease, the use of pesticides, and a decrease in the number of wild flowers. Climate change probably exacerbates the problem.<ref>Template:Cite journal</ref> This is a major cause of concern, as it can cause biodiversity loss and ecosystem degradation as well as increase climate change.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Contract pollination has overtaken the role of honey production for beekeepers in many countries. After the introduction of Varroa mites, feral honey bees declined dramatically in the US, though their numbers have since recovered.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> 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.<ref name="Penn">Template:Cite news</ref> In 2010 invertebrate iridescent virus and the fungus Nosema ceranae were shown to be in every killed colony, and deadly in combination.<ref>Johnson, Kirk (6 October 2010) Scientists and Soldiers Solve a Bee Mystery Template:WebarchiveTemplate:Cbignore. The New York Times.</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>Template:Cite journal</ref><ref>"Honey bees in US facing extinction" Template:Webarchive, The Daily Telegraph (London), 14 March 2007.</ref> Winter losses increased to about 1/3.<ref>Benjamin, Alison (2 May 2010) Fears for crops as shock figures from America show scale of bee catastrophe Template:Webarchive. The Observer (London).</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Varroa mites were thought to be responsible for about half the losses.<ref>Template:Cite news</ref>
Apart from colony collapse disorder, losses outside the US have been attributed to causes including pesticide seed dressings, using neonicotinoids such as clothianidin, imidacloprid and thiamethoxam.<ref>Template:Cite journal</ref><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> From 2013 the European Union restricted some pesticides to stop bee populations from declining further.<ref>Template:Cite news</ref> In 2014 the Intergovernmental Panel on Climate Change report warned that bees faced increased risk of extinction because of global warming.<ref>Gosden, Emily (29 March 2014) Bees and the crops they pollinate are at risk from climate change, IPCC report to warn Template:Webarchive The Daily Telegraph (London). Retrieved 30 March 2014</ref> In 2018 the European Union decided to ban field use of all three major neonicotinoids; they remain permitted in veterinary, greenhouse, and vehicle transport usage.<ref>Template:Cite news</ref>
Farmers have focused on alternative solutions to mitigate these problems. By raising native plants, they provide food for native bee pollinators like Lasioglossum vierecki<ref name="Farming for native bees">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> and L. leucozonium,<ref name="An Assessment of Non-Apis Bees as Fruit and Vegetable Crop Pollinators in Southwest Virginia">Adamson, Nancy Lee. An Assessment of Non-Apis Bees as Fruit and Vegetable Crop Pollinators in Southwest Virginia Template:Webarchive. Diss. 2011. Web. 15 October 2015.</ref> leading to less reliance on honey bee populations.
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Squash bees (Apidae) are important pollinators of squashes and cucumbers.
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Bee covered in pollen
As food producersEdit
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 dated to 15,000 BC.<ref name=EHSTMNWC/> Honey bees are used commercially to produce honey.<ref>Template:Cite book</ref>
As foodEdit
Bees are considered edible insects. People in some countries eat insects, including the larvae and pupae of bees, mostly stingless species. They also gather larvae, pupae and surrounding cells, known as bee brood, for consumption.<ref name=Holland2013>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> 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.<ref name=Tasty2015>{{#invoke:citation/CS1|citation |CitationClass=web }} (This particular Botok recipe uses anchovies, not bees)</ref><ref name=Sayangi2015>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Bee brood (pupae and larvae) although low in calcium, has been found to be high in protein and carbohydrate, and a useful source of phosphorus, magnesium, potassium, and trace minerals iron, zinc, copper, and selenium. In addition, while bee brood was high in fat, it contained no fat soluble vitamins (such as A, D, and E) but it was a good source of most of the water-soluble B vitamins including choline as well as vitamin C. The fat was composed mostly of saturated and monounsaturated fatty acids with 2.0% being polyunsaturated fatty acids.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>
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Bee larvae as food in the Javanese dish botok tawon
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Fried whole bees served in a Ukrainian restaurant
As alternative medicineEdit
Apitherapy is a branch of alternative medicine that uses honey bee products, including raw honey, royal jelly, pollen, propolis, beeswax and apitoxin (Bee venom).<ref name=MedicineWorld>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> The claim that apitherapy treats cancer, which some proponents of apitherapy make, remains unsupported by evidence-based medicine.<ref name=Cass>Template:Cite book</ref><ref name=Ades2009>Template:Cite book</ref>
StingsEdit
The painful stings of bees are mostly associated with the poison gland and the Dufour's gland which are abdominal exocrine glands containing various chemicals. In Lasioglossum leucozonium, the Dufour's Gland mostly contains octadecanolide as well as some eicosanolide. There is also evidence of n-triscosane, n-heptacosane,<ref name=":4">Template:Cite journal</ref> and 22-docosanolide.<ref name=":7">Template:Cite journal</ref>
See alsoEdit
Explanatory notesEdit
ReferencesEdit
External linksEdit
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- "Apoidea" at All Living ThingsTemplate:Sndimages, identification guides, and maps of bees
- Bee Genera of the World
- Anthophila (Apoidea) – BeesTemplate:SndNorth American species of bees at BugGuide
- Native Bees of North America at BugGuide
- "Bee declines driven by combined stress from parasites, pesticides, and lack of flowers"Template:SndScience
Template:Hymenoptera Template:Insects in culture Template:Taxonbar Template:Authority control