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East African lowland honey bee

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408:), a fitness advantage that allowed them to become an invasive species. A study by Fewell and Bertram was conducted to understand the source of these differences. The differences in fitness strategy were thought to be accounted for by the fact that African worker bees have a greater preference for pollen over nectar, which is a direct food resource for the emerging brood. Another important factor was thought to be differences between the species in age polyethism, or the allotment of different tasks as a honey bee ages. Young worker bees focus on in-hive assistance such as brood care, and the relatively younger African bee populations were thought to be one explanation for the emphasis on reproduction and colony expansion in the species. The study was also interested in the role different colony social environments and different genetic variation might play in the fitness discrepancies between the two subspecies. 354: 312:
have died as a result of 100–300 stings, it has been estimated that the average lethal dose for an adult is 500–1,100 bee stings. In terms of industrial honey production, in its natural habitat and the neo-tropics, the African bee produces far more honey than its European counterparts. It is unclear if this is due to a superior nectar gathering ability, lack of adaptability in the European honey bees for tropical environment, or both. Producing more swarms and absconding (abandoning its nest) are also examples of adaptive traits for tropical environment. In times of prolonged dearth they would migrate to a better food source area, a strategy applied also by
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A bee population must strike a balance in the distribution of resources towards the growth of the current colony members versus reproduction. If too much energy is expended on the maintenance of an adult colony, the bees will lose the chance to expand through reproduction but they will have older workers who specialize in nectar resources for energy (honey.) If too much energy is spent on reproduction, such a colony will be less equipped to survive drastic seasonal changes because they have younger workers who specialize in pollen for feeding the brood, not energy storage.
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and it is more evolutionarily favorable for them to store nectar and honey. African bees are more vulnerable to less predictable times of scarcity or attack and it is therefore to their advantage to produce as many young as possible, increasing the likelihood that some or even many will survive. Such circumstances would have favored the worker bees who preferred harvesting nectar in European colonies and pollen in African colonies, providing an explanation for how a divergence in worker behavior and age distribution evolved in
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advantage is so great that it is still more energetically favorable for a honey bee to collect warm nectar, even at low sugar concentrations (10%). Honey bees are energetically rewarded by harvesting nectar that is warmer than ambient temperatures because they make up for energy loss during foraging and obtain more nectar more easily.
318:, rather than waiting for a better season (European and Oriental bees). The lack of significant energy needs for thermoregulation of the brood nest in the tropics corresponds to a very rapid build-up of even the smallest african colonies, the higher in numbers and smaller in size swarming strategy makes perfect sense. 599:
preserving the propagation of their genes and contributing to their inclusive fitness. The parasitic model is more advantageous by comparison because it allows workers to directly reproduce offspring that are more closely related to them and greater in number, so they are a component of direct fitness.
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The underlying hypothesis for the aggressive behavior of East African lowland honey bees is based on the idea that this race of bees evolved in an arid environment, where the bees' food was scarce. Under this situation, selection favored more aggressive colonies, which protected their food source and
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The multifaceted aspect of communication in social insects makes social insect colonies easy to hijack. Especially in the case of closely related species and subspecies, the biology and organization of potential host species are similar to that of potential parasitizing species, making them easier to
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Although many pheromones contribute to reproduction, pheromones made in the mandibular gland of queens have been closely linked to reproduction, and they are produced by workers that reproduce. The pheromones prevent others from attacking them, induce workers to recognize them as queen, and give them
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These two strategies have been adopted by the European and African bees, respectively. European bees must survive the winter, an annual event with predictable mortality outcomes. Trying to meet the energetic needs of the colony and reproduction might decrease their overall survival during the winter
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Over time, distributions of the genotypic traits for worker food preference must have clustered around those conferring a proclivity towards resources that improved the fitness of the subspecies. The balancing of evolutionary costs and benefits have shaped the distribution of these genotypic traits.
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It appears that the cost of harvesting less-viscous nectar is that it is also less concentrated in sugar and would be an energetic loss for the honey bees. However, this is not the case; the speed of harvesting nectar with less viscosity increases the quantity harvested at a given time. The relative
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than a single European bee sting, though East African lowland honey bees respond more quickly when disturbed than do European honey bees. They send out three to four times as many workers in response to a threat. They will also pursue an intruder for a greater distance from the hive. Although people
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queen. Social parasitism in the social insects can involve various forms of exploitation that disrupt the normal division of labor in the colony. The recent development of technology to study the genetic makeup of colonies has revealed that the offspring contribution of reproducing worker parasites
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reproductive rate. For example, having fewer or relatively older workers who prefer nectar means that the colony will not have the resources available to rapidly or efficiently feed new broods. Worker food preferences have been connected to genotypic variation at specific quantitative trait loci.
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includes the southern and eastern regions of Africa. The species was first imported across the Atlantic Ocean to Brazil before it spread to Central America, South America, and southern areas of the United States. The Africanized honey bee thrives in tropical areas and is not well adapted for cold
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Nectar that is highly concentrated in sugar is more viscous and therefore reduces the speed of consumption and the size of honey bee crop loads. In cooler ambient temperatures, harvesting small, concentrated quantities of nectar does not allow honey bees to maintain the metabolism necessary for
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worker parasites is an example of an alternative evolutionary strategy that allows them to increase their "direct fitness in foreign colonies rather than inclusive fitness in their natal nests." Workers usually focus their efforts on raising and caring for larvae that are related to them, thus
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workers are able to disregard host queen signals. Pheromonal differences between the subspecies is a subject that requires more in-depth investigation to understand how such parasitization is made possible. As mandibular pheromones were a focus of the Dietemann et al. study it is probable that
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Honey bees are challenged to balance energy consumption and replenishment in their pursuit of nectar. High thoracic temperatures required for foraging flight pose a thermoregulatory imbalance that honey bees attempt to alleviate by targeting particular viscosities and temperatures of nectar
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workers focused on pollen processing behaviors while European workers focused on nectar processing behaviors. African bees were also more likely to store pollen while European bees stored honey. The study found that worker food preferences determined whether the colony maintained a certain
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into northern South Africa poses a threat to East African lowland honey bees. If a female worker from a Cape honey bee colony enters an East African lowland honey bee nest, she is not attacked, partly due to her resemblance to the East African lowland honey bee queen. As she is capable of
618:. Organisms evolve reproductive strategies that ensure the survival and propagation of the organisms’ genes. Successful reproductive strategies cope with particular economic constraints experienced by the organism. The parasitic relationship between 538:
queen. The worker parasites and their increasing number of clones become the sole reproductive individuals in the colony. The destruction of the division of labor leads to reduced resources that eventually force the colony to leave or perish.
440:, and this is thought to be related to the fact that African colonies have a younger, skewed age distribution by comparison. However, this is not a direct cause for the different subsistence strategies between the two subspecies. 326:
The appearance of the East African lowland honey bee is very similar to the European bee. However, the East African lowland honey bee is slightly smaller. Its upper body is covered in fuzz, and its abdomen is striped with black.
466:. Fewell and Bertram’s study is significant in that it provides a plausible method through which the fitness characteristics of the subspecies could have evolved from a small number of behavioral differences in worker bees. 512:
colonies in northern South Africa. The monopoly of this single lineage shows that they were able to subvert queen regulation of reproduction and worker recognition mechanisms. Dietemann et al. was able to prove that
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foraging flight. Harvesting warmer, less-viscous nectar is advantageous because of the energy gained by heat. Honey bees are able to stabilize their body temperature and make up for the energy lost by flying. In
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may have gained evolutionary advantage because, compared to other related species, it is not susceptible to the host queen’s pheromonal reproductive suppression of workers. The non-invasive varieties of
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The main difference found between African and European honey bees were a few behavioral traits in the worker bees that were all related to the workers’ food preference. It was found that
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hive from predators and robbed bees from other colonies. This behavior allowed more aggressive colonies to survive where the less aggressive colonies eventually were selected against by
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is an example of how a normally successful strategy of chemical recognition and maintenance of a reproductive division of labor can be undermined by competing, exploitative strategies.
377:, it was found that crop loads were largely contained in the abdomen, though it remains unclear whether this balances out the aforementioned energy loss from the thorax during flight. 594:
infiltrate. On the other hand, potential parasites face the challenge of being discovered by the host queen, usually the sole reproductive individual in the colony. The existence of
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The bumblebee’s ability to differentiate flower warmth by color and target warmer flowers is one noted precedent for nectar temperature selection in honey bees.
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queen signal correctly or a resistance to the signal. Ultimately this is an interesting example of a preexisting weakness towards social parasitism by
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Hartel, S; Neumann P; Raassen FS; Moritz RFA; Hepburn HR (2006). "Social parasitism by Cape honeybee workers in colonies of their own subspecies (
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workers are greatly under-represented in the foraging force), the death of the queen, and, before queen death, competition for egg laying between
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Hoover, SER; Higo HA; Winston ML (2006). "Worker honeybee ovary development seasonal variation and the influence of larval and adult nutrition".
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Dietemann, Vincent; Jochen Pflugfelder; Stephan Hartel; Peter Neumann; Robin M. Crewe (6 October 2006). "Social parasitism by honeybee workers (
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Fewell, Jennifer H.; Susan M. Bertram (2002). "Evidence for genetic variation in worker task performance by African and European honeybees".
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Winston, ML; OR Taylor; GW Otis (1983). "Some differences between temperate European and tropical African and South American honeybees".
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queens while in their presence. The resulting breakdown of the division of labor leads to desertion or death of the parasitized colony.
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produce less mandibular secretions than the invasive strain. In addition, they produce secretions that are not as similar to that of
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Heyneman, AJ (1983). "Optimal sugar concentrations of floral nectars: dependence on sugar intake efficiency and foraging costs".
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Neumann, P; Moritz RFA (2002). "The Cape honeybee phenomenon: they sympatric evolution of a social parasite in real-time".
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reproduction, she may begin laying eggs which hatch as "clones" of herself, which will also lay eggs, causing the
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resources. In lower environmental temperatures where energy loss is more pronounced, it has been shown through
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that honey bees seek warmer, less-concentrated and less-viscous nectar, an energetically favorable behavior.
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Hartel, S; Neumann P; Kryger P; von der Heide C; Moltzer G-J; Crewe RM; van Praagh JP; Moritz RFA (2006).
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workers to increase in number. The death of the host colony results from the dwindling numbers of
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queens, suggesting that quality or content of pheromones rather than quantity may explain how
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Shafir S., Afik O (2007). "Effect of ambient temperature on crop loading in the honey bee,
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Page, RE; Robinson GE (1991). "The genetics of division of labour in honey bee colonies".
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have higher rates of colony growth, reproduction, and swarming than European honey bees (
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to and greater ability to mimic and overwhelm the pheromonal regulation by host queens.
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access to higher quality foods. They also stop other workers from turning reproductive.
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queens as that of the invasive strain. The single lineage was selected for its greater
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bees begin foraging for pollen significantly earlier than their European counterparts
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workers produce crucial pheromones, achieve reproductive status, and overthrow an
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Ruttner, F. 1988: Biogeography and Taxonomy of Honeybees. Springer Verlag, Berlin
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Giray, T; Guzman-Novoa E; Aron CW; Zelinsky B; Fahrbach SE; Robinson GE (2000).
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worker parasites were able to produce mandibular pheromones that mimic that of
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East African lowland worker bees entering and exiting a nest in a rock crevasse
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different glands contribute to the pheromones related to reproductive status.
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Fletcher, David J.C. (2009). "African(ized) Bees: Their History and Future".
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Nicolson, Susan; Leo de Veer; Angela Kohler; Christian W. W. Pirk (2013).
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Esch.): Evidence for pheromonal resistance to host queen's signals".
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East African lowland worker bees foraging on pollen of an introduced
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AG, Dyer; Whitney HM; Arnold SEJ; Glover BJ; Chittka L (2006).
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succeeded either because of an inability to recognize the host
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Seeley, TD (1978). "Life history strategy of the honey bee,
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hosts in the southern region of South Africa. Specifically,
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The "African" Honey Bee. The processes of Africanization
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Proceedings of the Royal Society B: Biological Sciences
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swarms by socially parasitic Cape honeybee workers (
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worker parasites create female clones and usurp the
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New York: Oxford University Press. pp.  1650: 500:colonies were moved into the vicinity of the 8: 1123:Hunt, G; Page R; Fondrk M; Dullum C (1995). 2223: 1657: 1643: 1635: 950:"Bees associate warmth with floral colour" 193: 40: 31: 1452: 1281: 1193: 1148: 965: 842: 693:Smithsonian Marine Station at Fort Pierce 589:Evolutionary advantages and disadvantages 299:females will seek out a new host colony. 717:From laying workers to social parasites 432:African bees are "precocious foragers"; 27:Subspecies of honey bee native to Africa 713:Moritz, R.F.A (2002) The Cape honeybee 667: 444:Trade-offs of two different strategies 287:workers that perform foraging duties ( 1571:An Introduction to Behavioral Ecology 7: 731: 729: 727: 576:queens produce more pheromones than 453:Evolution of life history strategies 1513:Behavioral Ecology and Sociobiology 1470:Journal of Comparative Physiology B 1378:Behavioral Ecology and Sociobiology 1045:Behavioral Ecology and Sociobiology 736:Rinderer, TE; Hellmich, RL (1981). 547:The single lineage of parasitizing 340:areas that receive heavy rainfall. 49:Worker bee (female) drinking water 25: 1741:Subspecies, Breeds and Phenotypes 1554:Holldobler, B; Wilson EO (1990). 543:Evolution of pheromone production 344:Foraging economics and bee habits 1264:McNally, L; Schneider S (1996). 58: 504:subspecies. Ten years later, a 35:East African lowland honey bee 1727:Bee learning and communication 1303:. Princeton University Press. 1011:10.1080/0005772X.1983.11097902 236:East African lowland honey bee 209:East African lowland honey bee 1: 1630:Apidologie.org — African Bees 1100:10.1016/s0065-2806(08)60093-4 1088:Advances in Insect Physiology 884:10.1127/entom.gen/29/2007/135 349:Nectar content and harvesting 1569:Davies, Nicholas B. (2012). 1297:Schmid-Hempel, Paul (1998). 789:. Smithsonian Marine Station 508:was found to be devastating 506:single clonal…worker lineage 394:A. mellifera scutellata 1871:Apis mellifera sinisxinyuan 1300:Parasites in Social Insects 1141:10.1093/genetics/141.4.1537 787:"Apis mellifera scutellata" 689:"Apis mellifera scutellata" 405:A. mellifera mellifera 399:A. mellifera ligustica 2470: 486:A. mellifera capensis 202:The natural ranges of the 2454:Insects described in 1836 2267:Apis mellifera scutellata 2237:Apis mellifera scutellata 2212:Honeybee Discovery Center 2123:Diseases of the honey bee 1850:Apis mellifera scutellata 1668:types and characteristics 1594:Dawkins, Richard (2006). 1533:10.1007/s00265-002-0518-7 1482:10.1007/s00360-005-0032-0 1431:Apis mellifera scutellata 1398:10.1007/s00265-006-0222-0 1342:10.1007/s00040-005-0857-2 1065:10.1007/s00265-002-0501-3 493:merits closer attention. 482:Apis mellifera scutellata 426:Apis mellifera scutellata 367:Apis mellifera scutellata 337:Apis mellifera scutellata 241:Apis mellifera scutellata 201: 192: 178:Apis mellifera scutellata 174: 167: 55:Scientific classification 53: 48: 39: 34: 2439:Western honey bee breeds 2190:Museums and insectariums 2102:Colony collapse disorder 2077:Varroa sensitive hygiene 1857:Apis mellifera siciliana 1836:Apis mellifera monticola 1822:Apis mellifera pomonella 1808:Apis mellifera artemisia 1801:Apis mellifera adansonii 1270:Environmental Entomology 870:(Hymenoptera: Apidae)". 719:Apidologie Special Issue 602:The invasive lineage of 388:Significance of foraging 267:The introduction of the 2449:Insects of South Africa 1996:Horizontal top-bar hive 1899:Apis mellifera unicolor 1878:Apis mellifera sossimai 1864:Apis mellifera simensis 1435:Apis mellifera capensis 1429:"Infestation levels of 1374:Apis mellifera capensis 1326:Apis mellifera capensis 715:Apis mellifera capensis 572:It was discovered that 477:Apis mellifera capensis 392:It has been noted that 258:Apis mellifera capensis 2063:Parasites and diseases 1892:Apis mellifera taurica 1885:Apis mellifera syriaca 1843:Apis mellifera remipes 1815:Apis mellifera litorea 1195:10.1093/beheco/11.1.44 835:10.1098/rspb.2013.1597 568:Pheromonal differences 421: 412:Behavioral differences 361: 335:The native habitat of 2444:Hymenoptera of Africa 1454:10.1051/apido:2006012 872:Entomologia Generalis 620:A. m. scutellata 616:A. m. scutellata 608:A. m. scutellata 574:A. m. scutellata 558:A. m. scutellata 536:A. m. scutellata 519:A. m. scutellata 510:A. m. scutellata 502:A. m. scutellata 490:A. m. scutellata 460:A. m. scutellata 434:A. m. scutellata 419: 375:A. m. scutellata 356: 285:A. m. scutellata 160:A. m. scutellata 2202:Bee Museum of Rhodes 2118:Topics in beekeeping 1717:Honey bee life cycle 768:American Bee Journal 464:A. m. ligustica 438:A. m. ligustica 2197:Malacca Bee Gallery 2097:Deformed wing virus 1988:BS National Beehive 1829:Apis mellifera meda 1763:Carniolan honey bee 1525:2002BEcoS..52..271N 1390:2006BEcoS..60..785D 1283:10.1093/ee/25.3.643 1227:1978Oecol..32..109S 1057:2002BEcoS..52..318F 911:1983Oecol..60..198H 624:A. m. capensis 612:A. m. capensis 604:A. m. capensis 596:A. m. capensis 582:A. m. capensis 578:A. m. capensis 554:A. m. capensis 549:A. m. capensis 532:A. m. capensis 515:A. m. capensis 498:A. m. capensis 293:A. m. capensis 289:A. m. capensis 281:A. m. capensis 2092:American foulbrood 1235:10.1007/bf00344695 1182:Behavioral Ecology 919:10.1007/bf00379522 525:Method and results 422: 362: 2421: 2420: 2406:Open Tree of Life 2229:Taxon identifiers 2220: 2219: 2082:Small hive beetle 2071:Varroa destructor 1788:Western honey bee 1783:Russian honey bee 1778:Maltese honey bee 1768:European dark bee 1691:Laying worker bee 1613:978-0-19-929115-1 1580:978-1-4051-1416-5 1109:978-0-12-024223-8 752:978-0-429-30874-1 657:Western honey bee 637:natural selection 250:western honey bee 232: 231: 146:A. mellifera 18:African honey bee 16:(Redirected from 2461: 2414: 2413: 2401: 2400: 2388: 2387: 2375: 2374: 2362: 2361: 2349: 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Springer. 1447:: 462–470. 1276:: 643–652. 1094:: 118–169. 112:Hymenoptera 2428:Categories 2054:Jenter kit 2039:Bee smoker 2034:Queen clip 2014:Hive frame 1921:Beekeeping 1712:Bee colony 1705:Life cycle 1686:Worker bee 1674:Bee castes 1441:Apidologie 793:1 November 698:2013-12-08 663:References 562:resistance 322:Appearance 246:subspecies 217: the 185:Lepeletier 92:Arthropoda 2141:Australia 2029:Hive tool 1992:Flow Hive 1972:Equipment 1953:Honeycomb 1696:Drone bee 1681:Queen bee 1666:Honey bee 1328:Esch.)". 1215:Oecologia 1188:: 44–55. 1005:: 12–21. 999:Bee World 899:Oecologia 630:Evolution 303:Character 278:parasitic 221:, and the 140:Species: 78:Kingdom: 72:Eukaryota 2372:2.858897 2307:11044201 2276:BugGuide 2252:Q2034820 2246:Wikidata 1958:Propolis 1926:Apiology 1732:Swarming 1556:The Ants 1541:12117374 1490:16228242 1406:25063876 1350:44927091 1251:12784020 1243:28308672 1129:Genetics 1073:22128779 976:16885975 935:32118291 927:28310487 853:23902913 643:See also 309:venomous 297:capensis 118:Family: 88:Phylum: 82:Animalia 68:Domain: 2359:1131133 2171:Ukraine 2156:Ireland 2146:Hungary 2087:Waxworm 1984:Beehive 1931:Beeswax 1521:Bibcode 1498:8253649 1437:Esch.)" 1414:1218222 1386:Bibcode 1223:Bibcode 1159:8601492 1150:1206885 1053:Bibcode 907:Bibcode 844:3735266 331:Habitat 248:of the 244:) is a 128:Genus: 108:Order: 102:Insecta 98:Class: 2398:235082 2385:212527 2333:121322 2294:APISMZ 1979:Apiary 1610:  1577:  1539:  1496:  1488:  1412:  1404:  1348:  1307:  1249:  1241:  1157:  1147:  1106:  1071:  984:432440 982:  974:  954:Nature 933:  925:  851:  841:  749:  225:  215:  207:  205:  187:, 1836 122:Apidae 2411:85741 2281:96155 2161:Nepal 2151:India 2111:Lists 1936:Honey 1722:Brood 1606:–88. 1537:S2CID 1494:S2CID 1410:S2CID 1402:JSTOR 1346:S2CID 1247:S2CID 1069:S2CID 980:S2CID 931:S2CID 743:(PDF) 2380:NCBI 2354:ITIS 2346:6362 2315:GISD 2302:GBIF 2289:EPPO 1608:ISBN 1575:ISBN 1486:PMID 1305:ISBN 1239:PMID 1155:PMID 1104:ISBN 972:PMID 923:PMID 849:PMID 795:2013 747:ISBN 622:and 474:The 462:and 402:and 234:The 133:Apis 2341:ISC 2320:325 2004:Nuc 1529:doi 1478:doi 1474:176 1449:doi 1394:doi 1338:doi 1278:doi 1231:doi 1213:". 1190:doi 1145:PMC 1137:doi 1133:141 1096:doi 1061:doi 1007:doi 962:doi 958:442 915:doi 880:doi 839:PMC 831:doi 827:280 772:149 639:. 614:in 2430:: 2408:: 2395:: 2382:: 2369:: 2356:: 2343:: 2330:: 2317:: 2304:: 2291:: 2278:: 2263:: 2248:: 2006:, 2002:- 1998:, 1994:, 1990:, 1604:66 1535:. 1527:. 1517:52 1515:. 1492:. 1484:. 1472:. 1445:37 1443:. 1439:. 1408:. 1400:. 1392:. 1382:60 1380:. 1358:^ 1344:. 1334:53 1332:. 1274:25 1272:. 1268:. 1245:. 1237:. 1229:. 1219:32 1217:. 1186:11 1184:. 1180:. 1153:. 1143:. 1131:. 1127:. 1102:. 1092:23 1090:. 1067:. 1059:. 1049:52 1047:. 1019:^ 1003:64 1001:. 978:. 970:. 956:. 952:. 929:. 921:. 913:. 903:60 901:. 876:29 874:. 847:. 837:. 825:. 821:. 803:^ 770:. 726:^ 691:. 679:^ 2010:) 1986:( 1658:e 1651:t 1644:v 1616:. 1583:. 1543:. 1531:: 1523:: 1500:. 1480:: 1457:. 1451:: 1416:. 1396:: 1388:: 1352:. 1340:: 1313:. 1286:. 1280:: 1253:. 1233:: 1225:: 1198:. 1192:: 1178:" 1161:. 1139:: 1112:. 1098:: 1075:. 1063:: 1055:: 1013:. 1009:: 986:. 964:: 937:. 917:: 909:: 886:. 882:: 855:. 833:: 797:. 755:. 701:. 256:( 238:( 211:, 20:)

Index

African honey bee

Scientific classification
Edit this classification
Eukaryota
Animalia
Arthropoda
Insecta
Hymenoptera
Apidae
Apis
A. mellifera
Trinomial name
Lepeletier

Cape honey bee
subspecies
western honey bee
Cape honey bee
Africanized bees
Cape honey bee
parthenogenetic
parasitic
venomous
Apis dorsata

foxtail agave
A. mellifera ligustica
A. mellifera mellifera

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