|Range of Apis florea|
The dwarf honey bee (or red 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.
- 1 Taxonomy and phylogeny
- 2 Description and identification
- 3 Distribution and habitat
- 4 Colony cycle
- 5 Breeding and lifespan
- 6 Diet
- 7 Foraging
- 8 Competition
- 9 Mating systems
- 10 Defense
- 11 Communication
- 12 Genetic diversity
- 13 Ecology
- 14 Human interaction
- 15 References
Taxonomy and phylogeny
Danish zoologist Johan Christian Fabricius first identified Apis florea in 1787. A. florea is a member of the Apis genus. The Apidae is a diverse family of bees including honey bees, orchid bees, bumble bees, stingless bees, cuckoo bees and carpenter bees. The name Florea is a personal name of Romanian origin. A. florea is native to southeast Asia, and therefore one of the most phylogenetically basal bees. This suggests that honeybees originated in this region, with A. florea being one of the oldest and potentially similar to ancestors; therefore its first appearance in phylogeny occurs before that of A. mellifera and A. cerena. A. mellifera most likely evolved from A. florea and then migrated to Europe. A. florea, a dwarf honeybee, is a sister species of Apis andreniformis. These sister species are the most ancient honeybee lineage, most likely diverging in the Bartonian era.
Description and identification
A. florea is called the dwarf honey bee due to its small size compared to other honeybees. A worker is typically 7–10 mm in body length and its overall coloration is red-brown. A colony builds a single, exposed comb usually on tree branches or shrubs. A. florea produce honey that is harvested and eaten in Thailand and Cambodia. They are excellent pollinators, which gives them an important ecological role in the places they inhabit. Drones carry a thumb-like bifurcation called the basitarsus, which is located two-thirds along the length of the tibia. The fimbriate lobe of A. florea has three protrusions and they sting using two stylet barbs.
Apis florea and its sister species together comprise the subgenus Micrapis, and are the most primitive of the living species of Apis, reflected in their small colony size, and simple nest construction. The exposed single combs are built on branches of shrubs and small trees. The forager bees do not perform a gravity-oriented waggle dance on the vertical face of the comb to recruit nestmates as in the domesticated Apis mellifera and other species. Instead, they perform the dance on the horizontal upper surface where the comb wraps around the supporting branch. The dance is a straight run pointing directly to the source of pollen or nectar the forager has been visiting. The distinctiveness of the two species A. florea and A. andreniformis was established unequivocally in the 1990s. A. florea is redder and old workers always have a red first abdomen (younger workers are paler in colour, as is the case in giant honey bees); A. andreniformis is generally darker and the first abdomen segment is completely black in old bees. Distinguishing characteristics of the dwarf honey bees are outlined below:
|Characteristic||A. florea||A. andreniformis|
|Body length (mm)||7-10||8-9|
|Proboscis length (mm)||3.11-3.37||2.797-2.798|
|Forewing length (mm)||6.17-6.74||6.43-6.49|
|Forewing width (mm)||2.12-2.32||2.17-2.21|
|Hindwing length (mm)||3.17-4.83||3.22-3.23|
|Hindwing width (mm)||1.36 ± 0.04||1.25-1.28|
|Vertical length (from
support bottom) (cm)
|12.0 ± 3||10.0 ± 3.3|
|Horizontal width (cm)||16.9 ± 5.3||12.2 ± 3.6|
|Branch diameter (cm)||0.8 ± 0.07||1.7 ± 1.7|
|Worker cell dimensions|
|Depth of cell (cm)||0.93 ± 0.07||0.76 ± 0.02|
|Width of 10 cells (cm)||2.98 ± 0.15||2.78 ± 0.23|
|Drone cell dimensions|
|Depth of cell (cm)||1.33 ± 0.07||1.45 ± 0.71|
|Width of 10 cells (cm)||4.88 ± 0.21||4.18 ± 0.24|
|Queen cell dimensions|
|Depth of cell (cm)||1.41 ± 0.15||1.24 ± 0.26|
|Internal diameter of cell (cm)||0.47 ± 0.09||0.54 ± 0.08|
Distribution and habitat
A. florea spans the continents of Asia and Africa and is most commonly seen in Southeastern Asia (Thailand),Northeastern part of India, China, and forested regions of the Middle East. A. florea reach a decision about a new nesting site via dancing. They decide on a site when the largest number of individuals dance in the direction of the new site. The workers use an auditory signal of piping to indicate a decision about a new site has been reached, with the top of the swarm lifting off into the air first, followed by the bottom of the swarm and then the middle reaching the air last, but all within one minute of the swarm’s initial lift off. Since dancing is a common mechanism of communicating about a new nesting site in both A. florea and A. mellifera, it is suggested that this form of nest site selection evolved in the common ancestor of Apis. However, A. florea do not re-evaluate a site before several individuals move to the new site like A. mellifera does. Instead, swarms travel to the new site as a group and leave to a new site if it is later discovered to be unsuitable. This makes searching for new sites a much faster process for A. florea, but not necessarily more accurate.
Apis florea are found in southeastern Asian countries, especially in Thailand, Iran, Oman, India, Myanmar, and some part of china, Cambodia, and Vietnam. They live in forest habitat but they are also pollinators of tropical fruit crops in Thailand. Apis florea build exposed nests always with a single comb on a single branch. If they are building a new nest near to the old one, they salvage the wax from the old nest. Other species of honeybee do not return to the old nest to the salvage wax, perhaps because of the risk of contaminating pathogens. This behavior is only observed in this species. Even within the species this behavior differs, the colonies that migrate less than 200 meters involve in the salvaging of the wax, but the colonies that migrate long distance do not return for the old wax.
The annual colony cycle of honeybees involves migration, swarming, and absconding. A. florea migrate seasonally from one habitat to another. This might increase colony fitness, as the honeybees search for new territories, resources, or a reduction in parasites. Once a colony has outgrown its hive space, it will reproduce via swarming. During warmer seasons like spring and summer, ambient temperatures allow honeybees to forage actively, and they will reproduce frequently. During the colder seasons of autumn and winter, colonies diminish in size because they depend on food stores. Before swarming, the colony will build queen cells in order for virgin queens to rear young queens. Before the new queens emerge, the colony’s workers search for a new nesting site. Afterwards, the bees will choose who stays and who goes. Similar to absconding behavior, the old queen will swarm while the new queens prepare for emergence.
Breeding and lifespan
In a single patriline, more workers mean the colony will produce more drones. High mating frequency in A. florea has been evolutionarily selected for as observed in other members of the genus. The average lifespan of a drone is 15.6 days, ranging from 6–41 days. The queen has a much longer lifespan consistent with the longevity of the colony. A. florea have workers that police to ensure that workers’ eggs are destroyed at twice the rate of queens’ eggs using oophagy. The queens’ eggs are marked as to avoid destruction by worker bees. Since this behavior is also observed in A. mellifera, this suggests that policing mechanism behaviors evolved before the divergence of the genus Apis.
A. florea adopt the open-comb branch site as an information center for foraging. The branch platforms serves as a location for bee dancing that conveys important foraging information to other bees. They are commonly seen foraging near branches and small bushes. They mainly forage for pollen and nectar as food sources as well as water and safety from predators. Their frequent foraging and long migration range displays their high degree of mobility. They tend to build combs at lower elevations, away from direct sunlight and on the peripheral side of plant branches. A. florea forage openly, unlike A. cerana that mostly forage in parts of the hive that are not visible. Dialect observed in A. florea does not correlate with foraging range. A. florea tend to have longer foraging durations when compared to other bees in this genus, perhaps because they require smaller territories at lower altitudes and build open-combs on branches or twigs. Their small size necessitates more time to forage for pollen or nectar because they have a limit on how much food they can carry. Therefore, it is worth the cost of foraging for a longer duration if it means gaining the benefit of a highly nutritious food source.
A. florea demonstrate aggressive behaviors when competing for territory. Additionally, they compensate for their small size and limited flight range with more aggressive behavior since their flight range is also limited. This suggests that aggressive behavior is naturally selected for in A. florea because it facilitates defending flowers in a smaller territory.
When a queen mates, the sperm is transferred into the spermatheca directly. Specifically, A. florea females produce no mucus as a sign of mating, unlike A. mellifera queens. A. florea males use a clasper organ at the hindleg to hold the queen’s leg during mating. Anatomical studies support the hypothesis that A. florea mate via direct sperm transfer. A. florea queens typically mate with 3-4 males. A. florea mate with fewer drones than A. mellifera. A. mellifera queens mate with as many as 25 drones and simply deposit spermatozoa in the oviducts of the queen, where only 10% of spermatozoa reach the spermatheca. Thus, A. florea use the more energetically efficient method of sperm transfer.
A. florea show highly specific social defense mechanisms when they sense predators nearby. For instance, they typically display hissing and shimmering behavior, in addition to nesting amidst dense foliage to camouflage themselves from potential predators. A more poignant example is the specific behavioral response they exhibit against their predominant predator, the O. smaragdina weaver ant. When these ants are in close proximity, the bees produce and deposit sticky barriers to obstruct their path. The guard bees take cover at this sticky zone and start to alert other bees using specific hissing sounds with the goal of preventing full blown raids by the ants. Over time, more bees are recruited to contribute to this sticky zone barrier which reinforces their defense.
Defending a large social honey bee colony containing several thousands of workers requires simultaneous action of many individuals, which ideally involved communication between workers, enabling coordinated action and a fast response. Apis florea employ a defensive strategy called "piping", in which one individual emits an initial warning signal ("piping"), which is followed 0.3-0.7 seconds later by a general response from a large number of bees ("hissing"). With a fundamental frequency of 384 ± 31 Hz that lasts 0.82 ± 0.35 seconds, piping is audible to the human ear. Hissing is a noisy, broad band signal that is also audible to the human ear and produced by slight movements of the bees' wings. Individuals close to the piping bee are the first to hiss, which spreads rapidly to neighbors until an impressive coordinated crescendo is produced by the entire colony. Piping and hissing are accompanied by workers ceasing activity such as foraging dancing and departures from the colony.
As social bees, A. florea require a mechanism of communication, especially when conveying important spatial information about foraging, including direction and distance. The time elapsed during the waggle phase when a dancer moves forward while shaking the abdomen from side to side indicates the distance to a site. The longer the waggle phase, the longer the distance to a site and vice versa. In order to indicate direction, A. florea workers orient the waggle phase in the direction of the site, while dancing on the crow of the nest or swarm. The precision of dance does not depend on the type of site i.e. nest sites or food patches. In other words, A. florea do not change the precision of the waggle dance to indicate a goal is a nest site or food patch, unlike A. mellifera, which do change precision when conveying information about food patches specifically. This suggests that A. florea do not prioritize nesting site nor food patch information by changing the precision of dance.
Even in a single nest there is high genetic diversity among the Apis florea bees. Since honey bee queens are polygamous, strong genetic variability exists. The tendency of this species to perform certain tasks is dependent on this variation. For example, fanning of the nest is done by specific set of workers, when the nest reaches a specific temperature threshold.
Division of labor
Apis florea's younger individuals work within the nests performing maintenance while older individuals are responsible for protection and foraging. Some specific tasks like fanning of the comb to maintain a stable temperature are done by a specific set of workers, which is genetically motivated. This is completed by patrilines because diverse patrilines respond to a specific temperature threshold. When a queen mates with multiple unrelated males, genotypically diverse workers emerge in the colony. These colonies may be more fit than genetically uniform colonies perhaps because they are able to tolerate a wider range of environmental conditions. In such cases, A. florea may use genetically based task specialization, in which highly related daughters of a haploid male have genetic predispositions to undertake certain tasks. This could explain why polyandry has evolved and been maintained.
Aside from their small size, simple exposed nests and simplified dance language, the lifecycle and behavior of this species is fairly similar to other species of Apis. Workers of A. florea, like those of the species A. mellifera, also engage in worker policing, a process where nonqueen eggs are removed from the hive. Queenless A. florea colonies have been observed to merge with nearby queen-right A. florea colonies, suggesting workers are attracted to queen bee pheromones.
In the presence of a multiply mated queen, eggs laid by workers are removed in a process called worker policing. Worker policing is thus a result of genetic conflicts of interest among workers used non-exclusively by honeybees and wasps. With worker policing, workers control the production of males by other workers in favor of reproduction by the queen. In a colony with a single, multiple mating queen, all workers are equally related to male eggs laid by the queen [relatedness (r) = 0.25]. However, each worker is more related to a male egg laid by itself (r=0.5) or a male egg laid by a full sister (r=0.375). So in a colony with a singly mated queen, workers do not eat each other's eggs since their own and other's eggs are more closely related to them than the queen eggs are. But Apis florea is multiply mated, which reduces relatedness of workers to the eggs laid by other workers. If they do not share the same father, then relatedness of a worker to her half sister's son is only 0.125, half that of her relatedness to her brothers. So in this case each worker wants to lay her own eggs but her sisters prevent it and worker policing occurs. As an evolutionarily stable strategy (ESS), workers thus compromise by raising the eggs laid by the queen only and removing any eggs laid by other workers. Interestingly, worker policing is therefore more beneficial to workers than rearing their own eggs because they are better able to ensure the survival of their genetic material through working policing as an ESS. This may explain why workers have inactive ovaries in queenright colonies of this multiply mated species.
Queenless colonies therefore face a reproductive dilemma. Once a colony becomes queenless, some workers activate their ovaries within just four days and lay eggs in a last effort to ensure gene survival before the colony disappears via absconding behavior. In queenless colonies, worker policing decreases as all workers lay male eggs. However, the dilemma occurs when other workers parasitize a queenless colony and thus worker policing may be re-installed to some extent in this case. Workers that contribute resources and/or time to a queenless colony may succumb to the Concorde fallacy, in which investing in a colony with high rates of parasitism diminishes reproductive success and the benefits of remaining within that colony. Therefore, queenless colonies are observed to abscond within three weeks of losing a queen. This further supports the notion that Apis florea prefer to have a queenright colony and use worker policing as an ESS.
The main parasites of both A. andreniformis and A. florea belong to the mite genus Euvarroa. However, A. andreniformis is attacked by the species Euvarroa wongsirii, while Euvarroa sinhai preys on A. florea and colonies of imported A. mellifera. The two species of Euvarroa have morphological and biological differences: while E. wongsirii has a triangular body shape and a length of 47–54 μm, E. sinhai has a more circular shape and a length of 39–40 μm.
Apis florea can migrate to a variety of diverse locations due to human introduction or of their own volition. It poses a threat to native insects like Apis mellifera because they compete for the same resources.
The most dominant predators for Apis florea are ants and other arthropods. Since A. florea use open-combs, they must protect their comb from the outside, specifically at site of a branch. They employ two lines of defense. The first is against any falling object like leaves or other debris. A. florea use the head-pushing technique to move obstructions. The second line of defense is against ants and other arthropods. They accomplish this by creating sticky or repellent barriers (see Defense against Predators).
A. florea have two main interactions with humans: hunting and tourism. In Asia, there is widespread hunting of these bees because they are harmless to humans and they also have social and cultural significance to the two main religions in Asia: Hindu and Buddhism. In Hindu culture, the honey from such bees represents “the blendedness of everything” and is served with other ingredients in a variety of traditional ceremonies. In Buddhist culture, gifting honey to fellow monks is considered equal to giving alms, one of the most expressive ways that one can reward a good deed. In addition to being widely hunted and holding high cultural value, honey hunting sites are considered tourist sites in places like Nepal. Increased deforestation due to industrialization has enhanced bee migration to areas which are less populated, thus human interaction is mainly limited to fairly rural regions of Asia.
- Gupta, Rakesh Kumar. Beekeeping for Poverty Alleviation and Livelihood Security. N.p., 2014. Web.
- Oldroyd, Benjamin P., and Siriwat Wongsiri. Asian honey bees: biology, conservation, and human interactions. Harvard University Press, 2009.
- Wongsiri, S., et al. "Comparative biology of Apis andreniformis and Apis florea in Thailand." Bee World 78.1 (1997): 23-35.
- Y. R. Wu & B. Kuang (1987). "Two species of small honeybee - a study of the genus Micrapis". Bee World. 68: 153–155.
- Otis GW (1991) Revised distribution of three recently recognised species of honey bees in Asia. Honeybee Sci 15:167-170. Print.
- Oldroyd, Benjamin P. et al. “Nest Site Selection in the Open-Nesting Honeybee Apis Florea.” Behavioral Ecology and Sociobiology 62.10 (2008): 1643–1653. Web.
- Makinson, James C et al. “Moving Home: Nest-Site Selection in the Red Dwarf Honeybee (Apis Florea).” Behavioral Ecology and Sociobiology 65.5 (2015): 945–958. Print.
- Duangphakdee, Orawan (October–December 2005). "Reinforcing a barrier – a specific social defense of the dwarf honeybee (Apis florea) released by the weaver ant (Oecophylla smaragdina)" (PDF). Apidologie. 36 (4): 505–511. doi:10.1051/apido:2005036.
- Deowanish, S., et al. "Biodiversity of dwarf honey bees in Thailand." Proc. 7th Int. Conf. Trop. Bees, Chiang Mai, Thailand. 2001.
- Hepburn, Randall, et al. "Comb Wax Salvage by the Red Dwarf Honeybee, Apis Florea F." Journal of Insect Behavior 23.2 (2010): 159-64. ProQuest. Web. 28 Mar. 2015.
- Pirk, Christian W., et al. "Economics of Comb Wax Salvage by the Red Dwarf Honeybee, Apis Florea." Journal of Comparative Physiology.B, Biochemical, Systemic, and Environmental Physiology 181.3 (2011): 353-9. ProQuest. Web. 28 Mar. 2015.
- Suwannapong, Guntima, Mark Eric, and James C Nieh. Biology of Thai Honeybees : Natural History and Threats. N.p., 2011. Print.
- Palmer, K.a., and B.P. Oldroyd. “Mating Frequency in Apis Florea Revisited (Hymenoptera, Apidae).” Insectes Sociaux 48.1 (2001): 40–43. Web.
- Breed, Michael D, Xiao-bao Deng, and Robert Buchwald. “Comparative Nestmate Recognition in Asian Honey Bees , Apis Florea , Apis Andreniformis , Apis Dorsata , and Apis Cerana.” Comparative and General Pharmacology 38 (2007): 411–418. Web.
- Halling, L et al. “Worker Policing in the Dwarf Bee Apis Florea.” Behavioral Ecology and Sociobiology 49.6 (2001): 509–513. Print.
- Sciences, E D P, and E D P Sciences. “Reinforcing a Barrier – a Specific Social Defense of the Dwarf Honeybee (Apis.” Apidologie 36 (2005): 505–511. Web.
- Narayanaswamy, R, and S Basavarajappa. “Nesting Attributes of Dwarf Bee , Apis Florea F . under Urban Ecosystem of Manasagangotri Campus, Mysore ,India.” 2.6 (2013): 6–15. Print.
- Dyer, F.C., and T.D. Seeley. “Dance Dialects and Foraging Range in 3 Asian Honey-Bee Species.” Behav. Ecol. Sociobiol. 28.4 (1991): 227–233. Web.
- Koiger, N.; Vorwohl, G., 1979: Competition for food among four sympatric species of Apini in Sri Lanka (Apis dorsata, Apis cerana, Apis florea and Trigona iridipennis). Journal of Apicultural Research, 182: 95-109.
- Koeniger, N, G Koeniger, and S Wongsiri. “Mating and Sperm Transfer in Apis Florea.” Apidologie 20.5 (1989): 413–418. Print.
- Sarma, Moushumi Sen, et al. "Worker piping triggers hissing for coordinated colony defence in the dwarf honeybee Apis florea." Zoology 105.3 (2002): 215-223.
- Beekman, Madeleine et al. “Dance Precision of Apis Florea - Clues to the Evolution of the Honeybee Dance Language?” Behavioral Ecology and Sociobiology 62.8 (2008): 1259–1265. Web.
- Jones, Julia C., Piyamas Nanork, and Benjamin P. Oldroyd. "The Role of Genetic Diversity in Nest Cooling in a Wild Honey Bee, Apis Florea." Journal of Comparative Physiology 193.2 (2007): 159-65. ProQuest. Web. 28 Mar. 2015
- Beshers, Samuel N., and Jennifer H. Fewell. "Models of Division of Labor in Social Insects." Annual Review of Entomology 46 (2001): 413. ProQuest. Web. 28 Mar. 2015.
- Oldroyd, Benjamin P.; Sylvester, H. Allen; Wongsiri, Siriwat; Rinderer, Thomas E. (1994-01-01). "Task specialization in a wild bee, Apis florea (Hymenoptera: Apidae), revealed by RFLP banding". Behavioral Ecology and Sociobiology. 34 (1): 25–30. doi:10.1007/BF00175455. ISSN 0340-5443.
- Crozier, R. H.; Page, R. E. (1985-12-01). "On being the right size: male contributions and multiple mating in social Hymenoptera". Behavioral Ecology and Sociobiology. 18 (2): 105–115. doi:10.1007/BF00299039. ISSN 0340-5443.
- Robinson, Gene E.; Page, Robert E. (1988-05-26). "Genetic determination of guarding and undertaking in honey-bee colonies". Nature. 333 (6171): 356–358. doi:10.1038/333356a0.
- Page, Robert E., and Gene E. Robinson. "The genetics of division of labour in honey bee colonies." Adv insect physiol 23 (1991): 117-169.
- Oldroyd, Benjamin P.; Rinderer, Thomas E.; Buco, Steven M. (1992-05-01). "Intra-colonial foraging specialism by honey bees (Apis mellifera) (Hymenoptera:Apidae)". Behavioral Ecology and Sociobiology. 30 (5): 291–295. doi:10.1007/BF00170594. ISSN 0340-5443.
- Oldroyd, Benjamin P.; Rinderer, Thomas E.; Harbo, John R.; Buco, Steven M. (1992-05-01). "Effects of Intracolonial Genetic Diversity on Honey Bee (Hymenoptera: Apidae) Colony Performance". Annals of the Entomological Society of America. 85 (3): 335–343. doi:10.1093/aesa/85.3.335. ISSN 0013-8746.
- Wongvilas, S., et al. "Interspecific and conspecific colony mergers in the dwarf honey bees Apis andreniformis and A. florea." Insectes Sociaux 57.3 (2010): 251-255.
- Nanork, Piyamas; Wongsiri, Siriwat; Oldroyd, Benjamin P. (2006-08-02). "The reproductive dilemmas of queenless red dwarf honeybee (Apis florea) workers". Behavioral Ecology and Sociobiology. 61 (1): 91–97. doi:10.1007/s00265-006-0239-4. ISSN 0340-5443.
- Dawkins, R.; Carlisle, T. R. (1976-07-08). "Parental investment, mate desertion and a fallacy". Nature. 262 (5564): 131–133. doi:10.1038/262131a0.
- Delfinado-Baker, M., E. W. Baker, and A. C. G. Phoon. "Mites (Acari) associated with bees (Apidae) in Asia, with description of a new species."American Bee Journal 129.9 (1989): 609-613.
- Moritz, Robin F., et al. "Invasion of the Dwarf Honeybee Apis Florea into the Near East." Biological Invasions 12.5 (2010): 1093-9. ProQuest. Web. 17 Apr. 2015.
- Oldroyd, Benjamin P., and Piyamas Nanork. “Conservation of Asian Honey Bees.” Apidologie 40.3 (2009): 296–312. Web.
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