Apis cerana

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Eastern honey bee
Apis cerana, Asiatic honey bee - Khao Yai National Park.jpg
Asiatic honey bee - Khao Yai National Park, Thailand
Apis Cerana Chiang Mai w queen P1011011-3.jpg
Apis cerana workers and queen (marked with red dot) from hive near Chiang Mai, Thailand
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Apidae
Genus: Apis
Species:
A. cerana
Binomial name
Apis cerana
Fabricius, 1793
Apis cerana distribution map.svg
Range of Apis cerana

Apis cerana, the eastern honey bee, Asiatic honey bee or Asian honey bee, is a species of honey bee native to South, Southeast and East Asia. This species is the sister species of Apis koschevnikovi and both are in the same subgenus as the western (European) honey bee, Apis mellifera . [1] [2] [3] [4] [5] A. cerana is known to live sympatrically along with Apis koschevnikovi within the same geographic location. [6] Apis cerana colonies are known for building nests consisting of multiple combs in cavities containing a small entrance, presumably for defense against invasion by individuals of another nest. [7] The diet of this honey bee species consists mostly of pollen and nectar, or honey. [8] Moreover, Apis cerana is known for its highly social behavior, reflective of its classification as a type of honey bee. [4]

Contents

The terms Apis cerana indica and Apis Indica [9] or Indian honey bee, [10] [11] is an historic term, with all Asian hive bees now referred to as Apis cerana. [12]

Taxonomy and phylogeny

Apis cerana Cerana.jpg
Apis cerana

Danish zoologist Johan Christian Fabricius described Apis cerana, also known as the eastern or Asian honey bee, in 1793. [2] The genus name Apis is Latin for "bee". The eastern honey bee is of the Apidae family, one of the most diverse families of bees, including honey bees, carpenter bees, orchid bees, bumblebees, cuckoo bees, and even stingless bees. [13]

In the past, there has been discussion that Apis cerana and Apis mellifera are simply distinct races of the same species. This is essentially due to overwhelming similarities in both morphology and behavior, as both are medium-sized bees (10-11mm) that generally build multiple comb nests inside cavities. Other honey bee species, including the giant honey bees Apis dorsata and Apis laboriosa , generally construct nests consisting of a single comb in open areas. [14] However, despite the striking similarities between Apis cerana and Apis mellifera, there is evidence to suggest that these two species are quite distinct; for example, mating between these species does not produce offspring. In addition, while Apis mellifera colonies can reach sizes of up to 50,000 or more individuals, Apis cerana colonies are relatively small, with only around 6,000 to 7,000 workers. [14] Moreover, Apis cerana is found predominantly in the Eastern Asian region of the world, while Apis mellifera is found predominantly in the Western European and African region of the world. [14] For these reasons, it has now been concluded that these are in fact two separate species, contrary to prior beliefs.

Infraspecific groupings

Historically, Apis cerana has been subdivided into eight subspecies according to Engel (1999); they are:

Recent genetic analysis, however, has determined that some of the subspecies described may have been inadvertent misidentifications of very similar sympatric species, including Apis koschevnikovi of Borneo and Apis nigrocincta of the Philippines. Apis cerana nuluensis of Borneo is also now generally considered to be a separate species, as Apis nuluensis. [16]

Geographical distribution of the six Apis cerana morphocluster groups (Radloff et al., 2010) Geographical distribution of the six Apis cerana morphocluster groups.png
Geographical distribution of the six Apis cerana morphocluster groups (Radloff et al., 2010)

Radloff et al. (2010) have instead chosen to subdivide Apis cerana into six main statistically defined populations based on morphotypes ("morphoclusters"), instead of infraspecific ranks, which they argue were invalidly established and not biologically meaningful. These morphoclusters are: [16]

  • Synonyms: A. skorikovi, A. c. abansis, A. c. abanensis, A. c. bijjieca, A. c. cathayca, A. c. cerana, A. c. fantsun, A. c. hainana, A. c. hainanensis, A. c. heimifeng, A. c. indica, A. c. japonica, A. c. javana, A. c. kweiyanga, A. c. maerkang, A. c. pekinga, A. c. peroni, A. c. skorikovi, A. c. shankianga and A. c. twolareca
  • Synonyms: A. c. indica and A. c. javana
  • Synonyms: A. philippina, A. c. philippina and A. c. samarensis
  • Synonyms: A. cerana, A. indica, A. javana, A. c. johni, A. lieftincki, A. peroni, A. vechti linda and A. v. vechti

Description and identification

The physical characteristics of Apis cerana individuals are very similar to those of other species in the genus Apis . The individuals in this genus are defined by long, erect hairs that cover the compound eyes and assist in pollen collection, strongly convex scutellum, and a jugal lobe in the hindwing. Adult Apis cerana are black in color, with four yellow abdominal stripes. There are also distinctions between worker bees, queens, and drones. Worker bees are characterized by a pollen press on the hind leg to transport pollen, as well as a stinger in the place of an organ for laying eggs. Queens, which are the reproductive females, are typically larger than worker bees due to their enlarged reproductive organs. Drones, which are the males of the species, are defined by larger eyes, lack of a stinger, and a blunter abdominal shape. [4]

Distribution and habitat

Apis cerana encompass a wide range of climatic zones including moist tropical rainforests, wet-dry tropical savannas, mid-latitude steppes, dry mid-latitude grasslands, moist continental deciduous forests, and taigas. [16] The natural range of Apis cerana extends from Primorsky Krai in Russia in the north, to eastern Indonesia in the south; and to Japan in the east, to as far as the highlands of Afghanistan in the west. Countries they are native to include Afghanistan, Bangladesh, Bhutan, Brunei, Cambodia, China, India, Indonesia, Japan, Laos, Malaysia, Myanmar, Nepal, North Korea, Pakistan, the Philippines, Russia, South Korea, Sri Lanka, Taiwan, Thailand, Timor-Leste, and Vietnam. It was introduced deliberately to New Guinea in the 1970s, and has since spread into the Torres Strait Islands into Australia and the Solomon Islands. [17] [16] [18] Although the species was naturally clustered in East Asia, it has now expanded to various regions across the world as a result of human interference, with particular concern about its invasive potential in Australia as nests are found in a variety of environments, including both natural and man-made (see below). [16]

Nest

As a type of honey bee, Apis cerana must collect and store around a third of its nectar in a concentrated form in order to ensure an adequate supply for consumption during the harsh winter. [19] The nest is multi-combed and somewhat insulated, allowing the species to achieve optimal nest temperatures and thereby optimize foraging at early hours. The nest itself is a simple vertical comb made from wax secreted by workers, while the thermoregulation is generated by fanning and water evaporation from water collected in the field. [4] This large-scale storage tactic requires the construction of a stable and sturdy comb structure for such honey storage. However, as the production of beeswax for a comb is an energetically expensive endeavor, colonies do not generally build the entire structure very early on. Instead, the colony builds a smaller set of combs that satisfies the initial storage needs. Upon moving into the new nest, the colony will then continue to enlarge the combs until there are enough storage units to sufficiently account for all of the required honey. In general, the initial set of combs may account for around 20,000 cells, while the final, completed structure may contain up to 100,000. [19] These nests are typically large enough to host around 6,000 to 7,000 individuals and are found in a wide range of external environments. [14]

Nest thermoregulation

A. cerana maintains internal hive temperatures with a precision similar to that of A. mellifera, using similar mechanisms. A. cerana maintain body temperatures in a range of 33–35.5 °C even while ambient temperatures vary between 12 and 36 °C. This mechanism clearly shows them to possess effective nest thermoregulation systems. During summer, A. cerana employs evaporative cooling, where the worker bees cluster outside the nest in hot weather and fan their wings, thus removing excess heat and moisture from the nest and decreasing the hive temperature.

Thermal defense

When an A. cerana hive is invaded by the Japanese giant hornet ( Vespa mandarinia ), about 500 Japanese honey bees (A. cerana japonica) surround the hornet and vibrate their flight muscles until the temperature is raised to 47 °C (117 °F), heating the hornet to death, but keeping the temperature still under their own lethal limit (48–50 °C). [20] [21]

Behavior

Colony cycle

The colony of Apis cerana, a typical honey bee, consists of several thousand female worker bees, one queen bee, and several hundred male drone bees. The colony is constructed inside beeswax combs inside a tree cavity, with a special peanut-shaped structure on the margins of the combs where the queens are reared. [19]

The colony's annual cycle in cold temperature regions begins shortly after the winter solstice, when the colony raises the core temperature of its cluster to about 34 degrees Celsius and starts to rear brood. At first, only around 100 bees are produced, but several thousand bees are developing by early spring. By late spring, the colony will have already attained full size, and will begin to reproduce. The colony then rears several new queens, and divides itself with about half the workers plus the old queen once the new queens have nearly matured. This new swarm then flies to a new tree branch, explores nest cavities, and then directs the other bees to the new site once satisfied with the location. [19]

During the remainder of summer and into the fall, the colonies in the new locations build combs, rear brood, and gather food to quickly rebuild their populations and food reserves prior to the arrival of winter. [19]

Division of labor

As a social species, Apis cerana colonies contain divisions of labor depending on what each member of the group is specialized to perform. There is generally only one queen bee whose sole responsibility it is to lay eggs; therefore, she is the mother of all the workers present in the colony. Apart from the queen bee, the remaining female bees are known as the worker bees, as these individuals perform all the tasks necessarily to maintain the hive including tending to the eggs, larvae, and pupae, foraging for food and water, cleaning the beehive and producing honey. These tasks are divided among the female worker bees by a factor of age. The remaining individuals are the males, known as the “drones,” whose only responsibility is to mate with a queen from another colony; therefore, drones are solely produced during the reproductive season.

Communication

The principal method of communication is the waggle dance, performed primarily when a worker bee discovers a rich source of pollen or nectar and wishes to share this knowledge with her fellow nest-mates. The waggle dance occurs deep inside the colony's hive, where the worker bee performs a brief reenactment of the recent journey to a patch of flowers. Neighboring bees observe and learn this dance and can then follow the same pattern, utilizing the odor of the flowers to fly in a certain path and arrive at the same destination. The bees following the informed worker bee will extend their antennae towards the dancer in order to detect the dance sounds, as the frequency of the bee's antennae closely matches the vibration frequency of its wings. [19] The overall direction and duration of each waggle is closely correlated with the direction and distance from the flower patch being described. [19]

Mating behavior

Within the honey bee colony, a queen bee typically mates with 10 or more males. [19] This extensive mating is performed in an effort to secure a great range of genetic variation in her colony to cope with diseases, as well as respond to nectar sources and a wide range of external stimuli. [19] Apart from the queen bee, the only other sexual members of the society are the male drones, whose only function is to mate with the queen, after which they will die. [14]

The exact time and place of Apis cerana mating is specific to the subspecies, often varying by local environment. For instance, in Sri Lanka, Apis cerana males typically aggregate beside a tree canopy as opposed to above a tree as is found in the Apis cerana subspecies of Japan. The most significant factor in determining mating time, however, is not ecological conditions, but rather the presence of drones of other species. Mating time decreases as the number of non-species drones present increases. [4]

Reproductive swarming

In A. cerana, reproductive swarming is similar to A. mellifera. A. cerana reproductive swarms settle 20–30 m away from the natal nest (the mother or primary colony) and stay for a few days before departing for a new nest site after getting information from scout bees. [19] Scout bees search for suitable cavities in which to construct the swarm's home. [19] Successful scouts come back and report the location of suitable nesting sites to the other bees by performing communication dances on the surface of the swarm cluster in the same way as for food sources. [19]

Absconding behavior

A. cerana has migration and absconding behavior, abandoning the current nest and building a new nest in a new location where an abundant supply of nectar and pollen is available. These bees usually do not store great amounts of honey, so they are more vulnerable to starvation if a prolonged shortage of nectar and pollen occurs. Absconding will start when not enough pollen and nectar are available. After the last brood emerges, the adult bees fill their honey stomachs from the hive's stores and swarm to establish a new nest at a new location. A. cerana has more absconding behavior than A. mellifera.

Life history

The development of worker bees in a colony is typical of that for any insect that undergoes complete metamorphosis as it includes the four stages of egg, larva, pupa, and adult. The embryo grows inside the egg for 3 days, consuming the protein-rich egg yolk. [19] Then it undergoes an 8-day larval stage, which is an intense feeding state involving honey, pollen, and brood food supplied by the adult bees. [19] Finally, there is construction of a wax pupa which then matures and gnaws through the wax cap of the cell to emerge as a young bee. [19]

Kin selection

Genetic relatedness within colonies

As one queen generally mates with over a dozen males, the genetic relatedness of the colony is biased and represents haplodiploid sex determination. If the queen bee lays unfertilized eggs with no paternal genetic contribution, the eggs will develop into drones. If the queen bee lays fertilized eggs with both maternal and paternal genetic contribution, the eggs will develop into females. In this system, virgin queens sharing the same father will have a genetic relatedness of 0.75 and those of different fathers will have a genetic relatedness of only 0.25. [19] The females workers in the colony are related to the queen's sons by a genetic relatedness of 0.25. [19] Such biasing results in the genes of some female worker bees being represented disproportionately in the virgin queens. [19]

Worker-queen conflict

Conflict may arise between workers and bees as female workers attempt to increase the propagation of their genes by biasing their queen-rearing efforts in favor of virgin queens sharing the same father. Although female worker bees do possess ovaries and can essentially produce viable eggs, this potential is almost never realized as long as the colony is ruled by a dominant queen. Therefore, the probability of personal reproduction by a worker bee is exceedingly low. “Worker policing,” which is the mutual prevention of reproduction by workers, could be the reason behind the conscious non-reproduction of female worker bees. [19] In other words, their fertility is controlled by queen signals. The queen honey bee informs workers of her presence by pheromones that she secretes from her mandibular glands. These signals are acquired by workers in close proximity to the queen and then spread to other workers in the colony, mainly by physical contact. In the presence of queen pheromone signals, the vast majority of workers refrain from activating their ovaries. Due to factors of genetic relatedness, an Apis cerana worker will often try to prevent other workers in her colony from reproducing, either by destroying worker-laid eggs, or by showing aggression towards workers attempting to lay eggs through worker policing. [19]

Interaction with other species

Diet

Adult worker bees predominantly feed on pollen and nectar or honey, though the nutritive value of pollen varies depending on the plant. Mixed pollens possess a high nutritive value and actually supply all the necessary materials for proper development of young animals. However, when dried, pollen quickly loses its nutritive value. [8]

In addition to feeding themselves, bees also feed each other through a process known as “food transmission.” Moreover, workers may also obtain food from the queen, while drones acquire food by ingesting material regurgitated by other drones. Queens themselves are fed larval food by the workers during their wintering season, thereby neither feeding on nor being fed honey. [8]

Water requirement

In addition to food requirements for diet, water also plays a key role in the growth and development of adult bees. In fact, the form of food has little to no influence on the longevity and life expectancy of the bee as long as there is ready availability of water. [8] This idea was further supported through experimental means concerning queen bees isolated in separate cages. Both groups were fed sugar candy as a control measure; however, the group that was fed water in addition to the sugar candy lived an average of two weeks or more compared to the other group which only survived a matter of three to four days. [8] Moreover, the importance of water intake for an adult bee's survival can be further understood through examination of diet and behavior during prime seasons, during which colonies of bees consume large amounts of water in order to dilute honey produced as well as to regulate temperature in the nest. [8]

Predators

Vespine wasps, endemic to Southeast Asia, are a major predator for Apis cerana, predominantly at their colonies throughout Southern Asia. This hawking predation is especially fierce during the autumn season when the wasps are most populous, predominantly during the morning and afternoon. This method involves the wasps taking up a position in front of the beehive, while facing outwards away from the entrance towards returning foragers. [22] Vespine wasps attempt to attack the honey bee quarry in an effort to gain provisions to aid in the development of their own offspring. [22]

Defense

As the Vespine wasps approach the entrance to the honey bee nest, more guard bees are alerted, which in turn increases their probability of being killed by heat-balling bees. Heat balling is a unique defense system in which several hundred bees surround the wasp in a tight ball and vibrate their muscles in an effort to produce heat and effectively kill the wasp inside. [22] Alternatively, however, in the presence of a wasp, the bees may also just withdraw into their nests and await the heat-balling circumstances to develop naturally. Furthermore, other bees may just decide to fly away as an evasive measure in times of conflict, often altering their specific flight styles in order to avoid predation. [22]

Thermal defense

When an A. cerana hive is invaded by the Asian giant hornet ( Vespa mandarinia ), about 500 Japanese honey bees (A. cerana japonica) surround the hornet and vibrate their flight muscles until the temperature is raised to 47 °C (117 °F), heating the hornet to death, but keeping the temperature still under their own lethal limit (48–50 °C). [20]

Wing shimmering

Although both Apis mellifera and Apis cerana suffer from predation from vespine wasps, one defense mechanism unique to Apis cerana is “wing shimmering”. [22] During this period of self-defense, bees collectively execute carefully timed waves of shimmering of their wings when approached by predators such as vespine wasps. [22] This appears to serve as a distraction technique of visual pattern disruption that results in confusing predators. [22] As a result, predators are unable to continue attacking additional bees.

Use of animal feces

A 2020 study in Vietnam found that Apis cerana use feces and even human urine to defend their hives against raids by hornets ( Vespa soror ), a strategy not replicated by their European and North American counterparts, [23] though collection and use of feces in nest construction is well known in stingless bees. [24] [25]

Pathogens and parasites affecting Apis cerana

Microsporidia

Apis cerana is the natural host to the microsporidian parasite Nosema ceranae, a serious pest of the western honey bee. [26] When first discovered near Beijing, China, in 1994, it was originally thought that Nosema ceranae was restricted to Apis cerana in the East Asian region. [27] However, it has now been confirmed that this parasite species is actually present in colonies of Apis mellifera as well, both in Taiwan as well as Spain, though the origins of its arrival in Europe are still unknown. [27] Bees infected with Nosema ceranae suffer reduced lifespans and increased mortality in the winter as well as poor buildup and reduced honey yield in the spring. [27]

Mites

Apis cerana has also coevolved with the mite Varroa jacobsoni and thus exhibits more careful grooming than A. mellifera, thus has an effective defense mechanism against Varroa that keeps the mite from devastating colonies. Other than defensive behaviors such as these, much of their behavior and biology (at least in the wild) is very similar to that of A. mellifera.

Viruses

Asian honey bees are often infected by Chinese Sacbrood virus (CSBV) which also infects A. mellifera . [28] [29] Sacbrood viruses (SBV) primarily affect the brood of the honey bee and causes larval death. [30] Infected larvae fail to pupate, and ecdysial fluid aggregates around the integument, forming the “sac” for which the disease is named. Infected larvae change in color from pearly white to pale yellow, and shortly after death they dry out, forming a dark brown gondola-shaped scale. [31] SBV may also affect the adult bee, but in this case obvious signs of disease are lacking. [32] [33]

An invasive species in Australia

Apis cerana was first detected in Australia in 2007. By 2012, it had spread across 500,000 hectares. [34] The impacts of Apis cerana on the Australian environment are not well known due to limited research. [35] However, according to Biosecurity Queensland (2103), the Apis cerana "is likely to compete for pollen and nectar with native birds, mammals and insects, and for nesting sites in tree crevices". [36] There is a strong possibility that Apis cerana will also compete for resources with commercial honey bees and affect primary producers who rely on their pollination services. Control costs are also significant and amounted to at least A$4 million up to 2011. [37]

Efforts to eradicate Apis cerana in Australia have failed. Although an eradication program commenced in 2007, a decision that it was not possible to eradicate Apis cerana was made in 2011. [35] The decision was controversial though, sparking a senate inquiry which concluded that it failed to apply the precautionary principle and assess the potential impacts of Apis cerana on biodiversity. [38]

The bee is known as the Asian honey bee in Australia, [5] and is regarded as a biosecurity threat. [39]

Genetic database

As of 2015 the Biomodeling Laboratory at Seoul National University had constructed an Asian honey bee transcriptome database using an advanced sequencing technique. [40]

Related Research Articles

<span class="mw-page-title-main">Honey bee</span> Colonial flying insect of genus Apis

A honey bee is a eusocial flying insect within the genus Apis of the bee clade, all native to mainland Afro-Eurasia. After bees spread naturally throughout Africa and Eurasia, humans became responsible for the current cosmopolitan distribution of honey bees, introducing multiple subspecies into South America, North America, and Australia.

<span class="mw-page-title-main">Hornet</span> Genus of eusocial wasp

Hornets are the largest of the eusocial wasps, and are similar in appearance to their close relatives yellowjackets. Some species can reach up to 5.5 cm (2.2 in) in length. They are distinguished from other vespine wasps by the relatively large top margin of the head. Worldwide, 22 species of Vespa are recognized. Most species only occur in the tropics of Asia, though the European hornet is widely distributed throughout Europe, Russia, North America, and north-eastern Asia. Wasps native to North America in the genus Dolichovespula are commonly referred to as hornets, but all of them are actually yellowjackets.

<span class="mw-page-title-main">Bee brood</span> Chamber of a beehive

In beekeeping, bee brood or brood refers to the eggs, larvae and pupae of honeybees. The brood of Western honey bees develops within a bee hive. In man-made, removable frame hives, such as Langstroth hives, each frame which is mainly occupied by brood is called a brood frame. Brood frames usually have some pollen and nectar or honey in the upper corners of the frame. The rest of the brood frame cells may be empty or occupied by brood in various developmental stages. During the brood raising season, the bees may reuse the cells from which brood has emerged for additional brood or convert it to honey or pollen storage. Bees show remarkable flexibility in adapting cells to a use best suited for the hive's survival.

<span class="mw-page-title-main">Queen bee</span> Egg-laying individual in a bee colony

A queen bee is typically an adult, mated female (gyne) that lives in a colony or hive of honey bees. With fully developed reproductive organs, the queen is usually the mother of most, if not all, of the bees in the beehive. Queens are developed from larvae selected by worker bees and specially fed in order to become sexually mature. There is normally only one adult, mated queen in a hive, in which case the bees will usually follow and fiercely protect her.

<span class="mw-page-title-main">Worker bee</span> Caste of honey bee

A worker bee is any female bee that lacks the reproductive capacity of the colony's queen bee and carries out the majority of tasks needed for the functioning of the hive. While worker bees are present in all eusocial bee species, the term is rarely used for bees other than honey bees, particularly the European honey bee. Worker bees of this variety are responsible for approximately 80% of the world's crop pollination services.

Nosema apis is a microsporidian, a small, unicellular parasite recently reclassified as a fungus that mainly affects honey bees. It causes nosemosis, also called nosema, which is the most common and widespread of adult honey bee diseases. The dormant stage of N. apis is a long-lived spore which is resistant to temperature extremes and dehydration, and cannot be killed by freezing the contaminated comb. Nosemosis is a listed disease with the Office International des Epizooties (OIE).

<span class="mw-page-title-main">Oriental hornet</span> Species of hornet

The Oriental hornet is a social insect species of the family Vespidae. It can be found in Southwest Asia, Northeast Africa, the island of Madagascar, the Middle East, Central Asia, and parts of Southern Europe. Oriental hornets have also been found in a few isolated locations such as Mexico and Chile due to human introduction. The Oriental hornet lives in seasonal colonies consisting of caste system dominated by a queen. The hornet builds its nests underground and communicates using sound vibrations. The hornet has a yellow stripe on its cuticle (exoskeleton), which can absorb sunlight to generate a small electrical potential, and this might help supply energy for digging. The adult hornet eats nectar and fruits and scavenges for insects and animal proteins to feed to its young. Because they are scavengers, the hornets may also serve as a transmitter of disease following consumption of infected plants. The hornets are a primary pest to honey bees, attacking bee colonies to obtain honey and animal proteins. The sting of an Oriental hornet can be quite painful to humans and some humans are allergic to stings.

<i>Varroa destructor</i> Species of mite

Varroa destructor, the Varroa mite, is an external parasitic mite that attacks and feeds on honey bees and is one of the most damaging honey bee pests in the world. A significant mite infestation leads to the death of a honey bee colony, usually in the late autumn through early spring. Without management for Varroa mite, honey bee colonies typically collapse within 2 to 3 years in temperate climates. These mites can infest Apis mellifera, the western honey bee, and Apis cerana, the Asian honey bee. Due to very similar physical characteristics, this species was thought to be the closely related Varroa jacobsoni prior to 2000, but they were found to be two separate species after DNA analysis.

This page is a glossary of beekeeping.

<span class="mw-page-title-main">Stingless bee</span> Bee tribe, reduced stingers, strong bites

Stingless bees (SB), sometimes called stingless honey bees or simply meliponines, are a large group of bees (from about 462 to 552 described species), comprising the tribe Meliponini (or subtribe Meliponina according to other authors). They belong in the family Apidae (subfamily Apinae), and are closely related to common honey bees (HB, tribe Apini), orchid bees (tribe Euglossini), and bumblebees (tribe Bombini). These four bee tribes belong to the corbiculate bees monophyletic group. Meliponines have stingers, but they are highly reduced and cannot be used for defense, though these bees exhibit other defensive behaviors and mechanisms. Meliponines are not the only type of bee incapable of stinging: all male bees and many female bees of several other families, such as Andrenidae and Megachilidae (tribe Dioxyini), also cannot sting.

<i>Apis florea</i> Species of bee

The dwarf honey bee, Apis florea, is one of two species of small, wild honey bees of southern and southeastern Asia. It has a much wider distribution than its sister species, Apis andreniformis. First identified in the late 18th century, Apis florea is unique for its morphology, foraging behavior and defensive mechanisms like making a piping noise. Apis florea have open nests and small colonies, which makes them more susceptible to predation than cavity nesters with large numbers of defensive workers. These honey bees are important pollinators and therefore commodified in countries like Cambodia.

<i>Apis andreniformis</i> Species of bee

Apis andreniformis, or the black dwarf honey bee, is a relatively rare species of honey bee whose native habitat is the tropical and subtropical regions of Southeast Asia.

<i>Apis koschevnikovi</i> Species of bee

Apis koschevnikovi, Koschevnikov's honey bee, is a species of honey bee which inhabits Malaysian and Indonesian Borneo, where it lives sympatrically with other honey bee species such as Apis cerana.

<i>Apis nigrocincta</i> Species of bee

Apis nigrocincta is a species of honey bee that inhabits the Philippine island of Mindanao as well as the Indonesian islands of Sangihe and Sulawesi. The species is known to have queens with the highest mating frequencies of any species of the tribe Apini.

<i>Apis dorsata</i> Species of insect

Apis dorsata, the rock bee or giant honey bee, is a honey bee of South and Southeast Asia. They are typically around 17–20 mm (0.7–0.8 in) long and nests are mainly built in exposed places far off the ground, like on tree limbs, under cliff overhangs, and under buildings. These social bees are known for their aggressive defense strategies and vicious behavior when disturbed. Though not domesticated, indigenous peoples have traditionally used this species as a source of honey and beeswax, a practice known as honey hunting.

<span class="mw-page-title-main">East African lowland honey bee</span> Subspecies of honey bee native to Africa

The East African lowland honey bee is a subspecies of the western honey bee. It is native to central, southern and eastern Africa, though at the southern extreme it is replaced by the Cape honey bee. This subspecies has been determined to constitute one part of the ancestry of the Africanized bees spreading through North and South America.

<span class="mw-page-title-main">Western honey bee</span> European honey bee

The western honey bee or European honey bee is the most common of the 7–12 species of honey bees worldwide. The genus name Apis is Latin for "bee", and mellifera is the Latin for "honey-bearing" or "honey carrying", referring to the species' production of honey.

<i>Apis cerana japonica</i> Subspecies of bee

Apis cerana japonica is a subspecies of the eastern honey bee native to Japan. It is commonly known as the Japanese honey bee. Analysis of mitochondrial DNA suggests that the ancestors of this subspecies came to Japan from the Korean Peninsula via Tsushima Island. Genetic differentiation between Japanese honeybees and Korean honeybees occurred about 20,000 years ago, which coincides with the separation of Japan's Tsushima Island from the Korean Peninsula due to sea level rise. They have been observed moving into urban areas in the absence of natural predators.

<span class="mw-page-title-main">Worker policing</span> Insects destroying eggs not laid by queen

Worker policing is a behavior seen in colonies of social hymenopterans whereby worker females eat or remove eggs that have been laid by other workers rather than those laid by a queen. Worker policing ensures that the offspring of the queen will predominate in the group. In certain species of bees, ants and wasps, workers or the queen may also act aggressively towards fertile workers. Worker policing has been suggested as a form of coercion to promote the evolution of altruistic behavior in eusocial insect societies.

References

  1. ↑ Srinivasan, M.R. (2004). "Biodiversity of Honeybees". Advances in management of productive insects. Coimbatore: TNAU Publications.
  2. 1 2 Engel, M.S. (1999) The taxonomy of recent and fossil honey bees (Hymenoptera: Apidae: Apis). Journal of Hymenoptera Research8: pp. 165–196.
  3. ↑ Photos of Apis cerana Archived February 26, 2007, at the Wayback Machine
  4. 1 2 3 4 5 Oldroyd, Benjamin P.; Wongsiri, Siriwat (2006). Asian Honey Bees (Biology, Conservation, and Human Interactions). Cambridge, Massachusetts and London, England: Harvard University Press. ISBN   0674021940.
  5. 1 2 "Reporting diseases". Bee Aware. Retrieved 24 May 2020.
  6. ↑ Koeniger, N.; Koeniger, G.; Tingek, S.; Kelitu, A. (1996). "Interspecific rearing and acceptance of queens between Apis cerana Fabricius, 1793 and Apis koschevnikovi Buttel-Reepen, 1906". Apidologie. 27 (5): 371–380. doi: 10.1051/apido:19960505 .
  7. ↑ Nanork, P., et al. "Social parasitism by workers in queenless and queenright Apis cerana colonies." Molecular ecology 16.5 (2007): 1107-1114.
  8. 1 2 3 4 5 6 Haydak, Maykola H. "Honey bee nutrition." Annual Review of Entomology 15.1 (1970): 143-156.
  9. ↑ Kellogg, Claude R. (1941). "Some Characteristics of the Oriental Honeybee, Apis indica F., in China". Journal of Economic Entomology. 34 (5): 717–719. doi:10.1093/jee/34.5.717.
  10. ↑ Barbier, Yvan. "Apis of the world". Atlas Hymenoptera. Retrieved 9 July 2020.
  11. ↑ "Factsheet - Apis mellifera (The Honey Bee)". Apis mellifera (The Honey Bee). Retrieved 9 July 2020.
  12. ↑ "Apis cerana group". Bees for development. 7 February 2018. Retrieved 9 July 2020.
  13. ↑ Michener, Charles Duncan. The bees of the world. Vol. 1. JHU Press, 2000.
  14. 1 2 3 4 5 Winston, Mark L. The biology of the honey bee. Harvard University Press, 1991.
  15. ↑ Pesenko, Yu. A.; Lelej, A. S.; Radchenko, V. G. & G. N. Filatkin. (1990) The Chinese wax bee Apis cerana cerana F. (Hymenoptera, Apoidea) in the Soviet Far East. Entomological Review (Washington) 69(3): 21–46.
  16. 1 2 3 4 5 6 7 8 9 10 11 12 Radloff, Sarah E.; Hepburn, Colleen; Randall Hepburn, H.; Fuchs, Stefan; Hadisoesilo, Soesilawati; Tan, Ken; Engel, Michael S.; Kuznetsov, Viktor (15 March 2010). "Population structure and classification of Apis cerana" (PDF). Apidologie. 41 (6): 589–601. doi:10.1051/apido/2010008. S2CID   32751472.
  17. ↑ Koetz, Anna (21 October 2013). "Ecology, Behaviour and Control of Apis cerana with a Focus on Relevance to the Australian Incursion". Insects. 4 (4): 558–592. doi: 10.3390/insects4040558 . PMC   4553504 . PMID   26462524.
  18. ↑ Koetz A. 2012. Spread of Apis cerana in Australia, 2007 – 2012; Asian honey bee Transition to Management Program. Queensland government Department of Agriculture, Fisheries and Forestry
  19. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 Seeley, Thomas D. The wisdom of the hive: the social physiology of honey bee colonies. Harvard University Press, 2009.
  20. 1 2 "Apis cerana "cooking" a hornet to death". Archived from the original (video) on 30 September 2011.
  21. ↑ Baker, Mike (3 May 2020). "Murder Hornets vs. Honeybees: A Swarm of Bees Can Cook Invaders Alive" . The New York Times. Retrieved 4 May 2020.
  22. 1 2 3 4 5 6 7 Tan, K.; Radloff, S. E.; Li, J. J.; Hepburn, H. R.; Yang, M. X.; Zhang, L. J.; Neumann, P. (2007). "Bee-hawking by the wasp, Vespa velutina, on the honeybees Apis cerana and A. mellifera". Naturwissenschaften. 94 (6): 469–472. doi:10.1007/s00114-006-0210-2. PMID   17235596. S2CID   7218693.
  23. ↑ Mattila, Heather R.; Otis, Gard W.; Nguyen, Lien T. P.; Pham, Hanh D.; Knight, Olivia M.; Phan, Ngoc T. (2020-12-09). Blenau, Wolfgang (ed.). "Honey bees (Apis cerana) use animal feces as a tool to defend colonies against group attack by giant hornets (Vespa soror)". PLOS ONE. 15 (12): e0242668. Bibcode:2020PLoSO..1542668M. doi: 10.1371/journal.pone.0242668 . PMC   7725375 . PMID   33296376.
  24. ↑ Basari, Norasmah; Ramli, Sarah; Mohd Khairi, Nur (2018). "Food reward and distance influence the foraging pattern of stingless bee, Heterotrigona itama". Insects. 9 (4): 138. doi: 10.3390/insects9040138 . PMC   6315735 . PMID   30314344.
  25. ↑ Jalil, A.H. (2014) Beescape for Meliponines: Conservation of Indo-Malayan Stingless Bees
  26. ↑ Ritter, Wolfgang Nosema ceranae Archived February 14, 2007, at the Wayback Machine Albert Ludwigs University of Freiburg
  27. 1 2 3 Paxton, Robert J., et al. "Nosema ceranae has infected Apis mellifera in Europe since at least 1998 and may be more virulent than Nosema apis."Apidologie 38.6 (2007): 558-565.
  28. ↑ Shan, Liu; Liuhao, Wang; Jun, Guo; Yujie, Tang; Yanping, Chen; Jie, Wu; Jilian, Li (November 2017). "Chinese Sacbrood virus infection in Asian honey bees (Apis cerana cerana) and host immune responses to the virus infection". Journal of Invertebrate Pathology. 150: 63–69. doi: 10.1016/j.jip.2017.09.006 . PMID   28916146.
  29. ↑ Sun, Li; Li, Ming; Fei, Dongliang; Hu, Ying; Ma, Mingxiao (October 15, 2017). "Chinese sacbrood virus infection in Apis mellifera, Shandong, China, 2016". Virus Research. 242: 96–99. doi:10.1016/j.virusres.2017.09.014. PMID   28942949.
  30. ↑ W. Ritter, Diagnostik und Bekampfung von Bienenkrankheiten, Gustav Fischer Verlag Jena, Stuttgart, Germany, 1996.
  31. ↑ L. Bailey, “Recent research on honeybee viruses,” Bee World, vol. 56, pp. 55–64, 1975.
  32. ↑ L. Bailey, “The multiplication and spread of sacbrood virus of bees,” Annals of Applied Biology, vol. 63, no. 3, pp. 483–491, 1969.
  33. ↑ Mingxiao, Ma; Ming, Li; Jian, Cheng; Song, Yang; Shude, Wang; Pengfei, Li (2011). "Molecular and Biological Characterization of Chinese Sacbrood Virus LN Isolate". Comparative and Functional Genomics. 2011: 409386. doi: 10.1155/2011/409386 . PMC   3061217 . PMID   21527980.
  34. ↑ Koetz A. 2012. Spread of Apis cerana in Australia, 2007 – 2012; Asian honey bee Transition to Management Program. Queensland government Department of Agriculture, Fisheries and Forestry.
  35. 1 2 Invasive Species Council (2014). "Biosecurity Failures in Australia: 12 Case Studies: 7. Asian Honey Bees" (PDF). Retrieved 9 July 2020.
  36. ↑ Biosecurity Queensland. 2013. Asian honey bees in Queensland. http://www.daff.qld.gov.au/animal-industries/bees/diseases-and-pests/asian-honey-bees Archived 2013-12-31 at the Wayback Machine ; retrieved 2017-05-28
  37. ↑ Department of Agriculture, Fisheries and Forestry. 2011, Communique: National group supports work of Asian Honeybee Coordination Group. 19 July 2011
  38. ↑ The Senate Rural Affairs and Transport References Committee; 2011; Science underpinning the inability to eradicate the Asian honey bee; Commonwealth of Australia
  39. ↑ "NT Biosecurity Strategy 2016-2026". Department of Primary Industry and Resources. 20 July 2016. Retrieved 24 May 2020.
  40. ↑ Reuber, B. (2015). 21st Century Homestead: Beekeeping. Lulu.com. p. 11. ISBN   978-1-312-93733-8 . Retrieved 9 July 2020.
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