Merops apiasterEuropean bee-eater

Ge­o­graphic Range

Eu­ro­pean bee-eaters (Merops api­aster) have a broad dis­tri­b­u­tion cov­er­ing much of Eu­rope and Africa with range es­ti­mates up to 11,000,000 square km. These mi­gra­tory birds can be found as far north as Fin­land and range as far south as South Africa, ex­tend­ing east into some Asi­atic coun­tries as well. Most com­monly, Eu­ro­pean bee-eaters will breed and nest in south­ern Eu­rope, then mi­grate south dur­ing au­tumn and win­ter. (BirdLife In­ter­na­tional 2009, 2009; White, et al., 1978)

Habi­tat

Eu­ro­pean bee-eaters are com­monly found near fresh­wa­ter sys­tems and in­habit a va­ri­ety of habi­tat types such as for­est, sa­vanna, shrub­land, grass­land, and agri­cul­tural areas. The habi­tat for nest­ing can be spe­cific in­volv­ing only river sys­tems or gravel pits with steep ex­posed banks. Eu­ro­pean bee-eaters have also been found to dig bur­rows di­rectly into the ground. Food avail­abil­ity can de­ter­mine the habi­tat oc­cu­pied by Eu­ro­pean bee-eaters. Many agri­cul­tural fields use bee-hives for pol­li­na­tion and M. api­aster will fre­quent those areas. (BirdLife In­ter­na­tional 2009, 2009; White, et al., 1978; Yosef, et al., 2006; BirdLife In­ter­na­tional 2009, 2009; White, et al., 1978; Yosef, et al., 2006)

Phys­i­cal De­scrip­tion

Eu­ro­pean bee-eaters are mid-sized in­sec­ti­vores that have dark, thick, and slightly down­ward curved bills. A bright yel­low chin and throat patch meet a blue chest that ex­tends down to the flanks and belly. Dark lores and eye-stripe are con­trasted by a white patch above the upper mandible and lower white eye-stripe ex­tend­ing from the lower mandible. A dark chest­nut color cov­ers the crown and nape, be­com­ing lighter in color on the back. Upper tail coverts are vari­able, rang­ing from green to blue, with most of the tail being blue. Wing lengths av­er­age 44 cm for males and 49 cm for fe­males. Weights of Eu­ro­pean bee-eaters are sim­i­lar in males and fe­males and range from 44 to 78 g. Total body length ranges from 27 to 30 cm.

Males and fe­males, very sim­i­lar in col­oration, can be dis­tin­guished by the hue of the greater coverts, being a chest­nut in males and green­ish-blue in fe­males, and by the me­dian coverts, where males are a chest­nut and fe­males have a green­ish hue. Ju­ve­niles can be dis­tin­guished from adults by the color of the iris. In ma­ture adults the iris is a vi­brant red and ju­ve­niles will have a gray­ish-olive-red color. Also, the chest­nut color found in adults is only green in ju­ve­niles. (Les­sells and Oven­den, 1989; Yosef, et al., 2006)

  • Sexual Dimorphism
  • sexes alike
  • Range mass
    44 to 78 g
    1.55 to 2.75 oz
  • Average mass
    52 g
    1.83 oz
  • Range length
    27 to 30 cm
    10.63 to 11.81 in
  • Average length
    28 cm
    11.02 in
  • Range wingspan
    44 to 49 cm
    17.32 to 19.29 in
  • Average wingspan
    46 cm
    18.11 in

Re­pro­duc­tion

Eu­ro­pean bee-eaters are monog­a­mous and will gen­er­ally stay to­gether from year to year if both sur­vive. Courtship feed­ing has been ob­served of some male Eu­ro­pean bee-eaters, where the male will bring food to the fe­male a cou­ple days be­fore, dur­ing, and after egg lay­ing. Roughly 20% of nest­ing pairs have 1 to 4 helpers that ex­hibit co­op­er­a­tive breed­ing, where a non-breed­ing male, likely a close rel­a­tive, will as­sist the nest­ing pair by sit­ting on the nest and catch­ing prey for young. (Avery, et al., 1988; Hoi, et al., 2002; Horváth, et al., 1992)

In cen­tral Eu­rope, most Eu­ro­pean bee-eaters re­turn to their breed­ing range in late April or early May. They will mate in May and dig out bur­rows around 1 m deep in sand pits or steep river banks. Fe­males lay 4 to 7 eggs in late May to early June. They are laid in 2 day in­ter­vals and in­cu­bated 3 to 4 weeks be­fore hatch­ing asyn­chro­nously. Be­fore young fledge asyn­chro­nously at around 4 weeks of age they un­dergo weight loss to re­duce their weight closer to that of an adult. Asyn­chro­nous Hatch­ing and fledg­ing is thought to help off­set sib­ling ri­valry and allow bet­ter care of young with a vari­able food source like fly­ing in­sects. Ju­ve­niles be­come in­de­pen­dent at 1 to 2 months of age. Sex­ual ma­tu­rity is reached within the first year, though ju­ve­niles are not al­ways suc­cess­ful at breed­ing in their first year. Ju­ve­niles may come back to the same colonies and nest near rel­a­tives such as par­ents or sib­lings. These ju­ve­niles may be­come fam­ily helpers if they fail to nest.

They are ei­ther soli­tary or colo­nial nesters. One study found a neg­a­tive ef­fect on nest suc­cess with in­creas­ing colony size. Iso­lated pairs with equal clutch size had a higher rate of nest­ing suc­cess. It is thought that colo­nial breed­ing could still be worth­while if it in­creases adult sur­vival. (Avery, et al., 1988; Les­sells and Avery, 1989; Les­sells and Oven­den, 1989)

  • Breeding interval
    European bee-eaters breed once yearly.
  • Breeding season
    European bee-eaters breed between May and June.
  • Range eggs per season
    4 to 7
  • Average eggs per season
    5
  • Range time to hatching
    3 to 4 weeks
  • Range fledging age
    28 to 32 days
  • Range time to independence
    1 to 2 months
  • Average age at sexual or reproductive maturity (female)
    1 years
  • Average age at sexual or reproductive maturity (male)
    1 years

Both male and fe­male Eu­ro­pean bee-eaters par­tic­i­pate in ex­ca­vat­ing the un­der­ground nest­ing bur­row. After the eggs are laid, the pair shares in­cu­ba­tion re­spon­si­bil­i­ties. Chicks are born al­tri­cial, with­out feath­ers and eyes closed, and rely on sig­nif­i­cant parental care for sur­vival. The male "helper" will also share in­cu­ba­tion and feed­ing du­ties, but is not as re­li­able as the breed­ing pair. Both par­ents pro­vide food and pro­tec­tion for young until fledg­ing. Some male Eu­ro­pean bee-eaters will con­tinue to feed the fe­male for sev­eral days dur­ing and after egg lay­ing.

Eu­ro­pean bee-eaters ex­hibit very spe­cific feed­ing be­hav­iors that are dif­fi­cult for young birds to learn. Breed­ing pairs will con­tinue to feed fledg­lings until the young learn the skills to suc­cess­fully for­age for them­selves. (Les­sells and Avery, 1989; Les­sells, et al., 1994)

  • Parental Investment
  • altricial
  • male parental care
  • female parental care
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • male
      • female
    • protecting
      • male
      • female
  • pre-weaning/fledging
    • provisioning
      • male
      • female
    • protecting
      • male
      • female
  • pre-independence
    • provisioning
      • male
      • female
    • protecting
      • male
      • female
  • post-independence association with parents
  • extended period of juvenile learning

Lifes­pan/Longevity

Eu­ro­pean bee-eaters have been doc­u­mented to live up to 5.9 years in the wild. ("Merops api­aster Lin­naeus 1758", 2009)

  • Range lifespan
    Status: wild
    5.9 (high) years

Be­hav­ior

Eu­ro­pean bee-eaters are mi­gra­tory, di­ur­nal birds that spend most of their time for­ag­ing for food. It is com­mon to see them sit­ting at a perch scan­ning for prey, then fly­ing out catch­ing a prey item and com­ing back to the perch to sub­due and con­sume it. These birds are often found nest­ing in colonies, but may also nest singly as well. Mixed colonies of Eu­ro­pean bee-eaters and blue cheeked bee-eaters (Merops per­si­cus) can be found for­ag­ing to­gether with­out com­pe­ti­tion be­cause of min­i­mal diet over­lap. (Bur­ton and Bur­ton, 2002; Kossenko and Fry, 1998)

  • Range territory size
    0.7 to 8 m^2

Home Range

Often found in colonies, ter­ri­to­ries are formed 0.7 to 8 m around nest­ing sites dur­ing breed­ing sea­son.

Com­mu­ni­ca­tion and Per­cep­tion

The fam­ily Merop­i­dae (bee-eaters), most species being colo­nial, often will ex­hibit in­ter­spe­cific and in­traspe­cific com­mu­ni­ca­tion. Like most colo­nial species, Eu­ro­pean bee-eaters are very vocal while within the colony. Pairs often call to lo­cate or oth­er­wise com­mu­ni­cate to each other. Eu­ro­pean bee-eaters have a lim­ited reper­toire, which con­sists of sev­eral, slight vari­a­tions on a "preep" call. This call is given in rapid suc­ces­sion while in so­cial groups, and takes on a "bub­bly" char­ac­ter­is­tic dur­ing courtship.

Eu­ro­pean bee-eaters have been found to ex­hibit in­traspe­cific “help­ing”. A nest­ing pair may ac­cept a third party to help with in­cu­bat­ing or feed­ing to in­crease nest­ing suc­cess. This so­cial com­mu­ni­ca­tion may be be­tween re­lated in­di­vid­u­als and help fit­ness.

Mixed flocks of Eu­ro­pean bee-eaters and blue cheeked bee-eaters (Merops per­si­cus) have been found to have bet­ter breed­ing suc­cess as a re­sult of mixed species for­ag­ing off­set­ting in­ter­spe­cific com­pe­ti­tion. In­ter­spe­cific com­mu­ni­ca­tion has also been found to be de­fen­sive dur­ing nest­ing, in­volv­ing fight­ing and avoid­ance, whereas in­traspe­cific com­mu­ni­ca­tion in­cluded sun­ning, preen­ing, and mob­bing of preda­tors. The ben­e­fit of being a so­cial com­mu­nal species is hav­ing more eyes on the look­out for dan­ger; Eu­ro­pean bee-eaters will use vocal com­mu­ni­ca­tion to warn oth­ers about dan­ger.

Like all birds, Eu­ro­pean bee-eaters per­ceive their en­vi­ron­ment through vi­sual, au­di­tory, tac­tile and chem­i­cal stim­uli. (Kossenko and Fry, 1998; Pe­trescu and Adam, 2001; White, et al., 1978)

Food Habits

As their name im­plies, Eu­ro­pean bee-eaters' diet con­sists of bees rang­ing in size from large to small (Hy­menoptera), but also in­cludes drag­on­flies (On­do­nata) and other fly­ing in­sects. Bee-eaters are quick on the wing and agile for catch­ing fly­ing in­sects. When catch­ing in­sects they will grasp them by the mid­sec­tion, fly back to perch, and hit them against their perch until move­ment ceases. When catch­ing sting­ing in­sects they will im­mo­bi­lize them and hit the sting against the perch to pull or rip it out, and then toss the prey up ver­ti­cally to swal­low. Breed­ing pairs of Eu­ro­pean bee-eaters con­tinue to feed their fledg­lings until the young birds learn to suc­cess­fully catch and eat in­sects. (Bur­ton and Bur­ton, 2002; Krebs and Avery, 1984)

  • Animal Foods
  • insects

Pre­da­tion

Mont­pel­lier snakes (Malpolon mon­spes­su­lanus), ocel­lated lizards (Timon lep­idus), and black kites (Mil­vus mi­grans) are com­mon preda­tors of Eu­ro­pean bee-eaters. Nestlings are most vul­ner­a­ble be­cause ground bur­rows are eas­ily ac­cessed by snakes and lizards. (Bur­ton and Bur­ton, 2002)

Ecosys­tem Roles

Eu­ro­pean bee-eaters are known as ecosys­tem en­gi­neers be­cause of their ef­fects on arid en­vi­ron­ments through bur­row­ing breed­ing be­hav­ior. Three ways have been sug­gested re­gard­ing how Eu­ro­pean bee-eaters im­pact the en­vi­ron­ment: (i) bur­row­ing and soil re­moval al­lows rain, sun­light, and nu­tri­ents to pen­e­trate soil. (ii) aban­doned bur­rows pro­vide shel­ter for other species to col­o­nize the area (iii) deep bur­rows pro­vide ac­cess to in­ver­te­brate prey items which can in­crease food web com­plex­ity.

The mi­cro­cli­mate that is cre­ated by these bur­rows can be sig­nif­i­cantly dif­fer­ent from the macro­cli­mate. Some species that re-use bur­rows made by Eu­ro­pean bee-eaters in­clude Eu­ro­pean rollers (Cora­cias gar­ru­lus), lit­tle owls (Athene noc­tua), pied wag­tails (Motacilla alba), and rock spar­rows (Petro­nia petro­nia).

Analy­sis of ac­tive Eu­ro­pean bee-eaters' nests de­tected sev­eral species of mites (chicken mites, trop­i­cal fowl mites) and lar­vae of Diptera, bee­tles (Tene­bri­on­idae fam­ily), and moths and but­ter­flies (Lep­i­doptera order). (Casas-Crivlle and Valera, 2005)

Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Eu­ro­pean bee-eaters have not been recorded as a species that ben­e­fits hu­mans in an eco­nomic man­ner. They are unique and beau­ti­ful birds that at­tract many bird­ers and pho­tog­ra­phers.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Eu­ro­pean bee-eaters are seen as a pest by many farm­ers in cen­tral and south­ern Eu­rope. These birds are at­tracted to high den­si­ties of cul­ti­vated bees, and are fre­quently per­se­cuted by farm­ers. Eu­ro­pean bee-eaters may cause sig­nif­i­cant dam­age to a hive if they prey upon the queen. (Al-Ghzawi, et al., 2009)

  • Negative Impacts
  • crop pest

Con­ser­va­tion Sta­tus

Eu­ro­pean bee-eaters are listed as a species of least con­cern by IUCN. Al­though their num­bers have been de­clin­ing over the past decade, the pop­u­la­tion (480,000 to 1,000,000 breed­ing in­di­vid­u­als) is still well above any level of threat. (BirdLife In­ter­na­tional 2009, 2009)

Con­trib­u­tors

Tyler Petroelje (au­thor), North­ern Michi­gan Uni­ver­sity, Alec Lind­say (ed­i­tor), North­ern Michi­gan Uni­ver­sity, Rachelle Ster­ling (ed­i­tor), Spe­cial Pro­jects.

Glossary

Ethiopian

living in sub-Saharan Africa (south of 30 degrees north) and Madagascar.

World Map

Palearctic

living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.

World Map

acoustic

uses sound to communicate

agricultural

living in landscapes dominated by human agriculture.

altricial

young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

colonial

used loosely to describe any group of organisms living together or in close proximity to each other - for example nesting shorebirds that live in large colonies. More specifically refers to a group of organisms in which members act as specialized subunits (a continuous, modular society) - as in clonal organisms.

cooperative breeder

helpers provide assistance in raising young that are not their own

desert or dunes

in deserts low (less than 30 cm per year) and unpredictable rainfall results in landscapes dominated by plants and animals adapted to aridity. Vegetation is typically sparse, though spectacular blooms may occur following rain. Deserts can be cold or warm and daily temperates typically fluctuate. In dune areas vegetation is also sparse and conditions are dry. This is because sand does not hold water well so little is available to plants. In dunes near seas and oceans this is compounded by the influence of salt in the air and soil. Salt limits the ability of plants to take up water through their roots.

diurnal
  1. active during the day, 2. lasting for one day.
endothermic

animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.

female parental care

parental care is carried out by females

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

insectivore

An animal that eats mainly insects or spiders.

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

male parental care

parental care is carried out by males

migratory

makes seasonal movements between breeding and wintering grounds

monogamous

Having one mate at a time.

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

riparian

Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).

scrub forest

scrub forests develop in areas that experience dry seasons.

seasonal breeding

breeding is confined to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

soil aeration

digs and breaks up soil so air and water can get in

solitary

lives alone

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

tropical savanna and grassland

A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.

savanna

A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.

temperate grassland

A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.

visual

uses sight to communicate

Ref­er­ences

2009. "Merops api­aster Lin­naeus 1758" (On-line). En­cy­clo­pe­dia of Life. Ac­cessed De­cem­ber 17, 2010 at http://​www.​eol.​org/​pages/​1050051.

Al-Ghzawi, A., S. Za­itoun, H. Shan­nag. 2009. In­ci­dence and Ge­o­graph­i­cal Dis­tri­b­u­tion of Hon­ey­bee (Apis mel­lif­era L.) Pests in Jor­dan. Ann. soc. en­to­mol. Fr., 45/3: 305-308.

Avery, M., J. Krebs, A. Hous­ton. 1988. Eco­nom­ics of courtship-feed­ing in the Eu­ro­pean bee-eater (Merops api­aster). Be­hav­ioral Ecol­ogy and So­cio­bi­ol­ogy, 23/2: 61-67.

BirdLife In­ter­na­tional 2009, 2009. "Merops api­aster" (On-line). In: IUCN 2009. IUCN Red List of Threat­ened Species.. Ac­cessed Jan­u­ary 12, 2010 at http://​www.​iucnredlist.​org/​apps/​redlist/​details/​142227/​0.

Bur­ton, M., R. Bur­ton. 2002. Bee-eaters. Pp. 180 in B Hoare, T Cooke, eds. In­ter­na­tional Wildlife En­cy­clo­pe­dia, Vol. 1, Third Edi­tion. Ter­ry­town, New York: Mar­shall Cavendish.

Casas-Crivlle, A., F. Valera. 2005. The Eu­ro­pean bee-eater (Merops api­aster) as an ecosys­tem en­gi­neer in arid en­v­iorn­ments. Jour­nal of Arid En­v­iorn­ments, 60/2: 227-238.

Heneberg, P. 2009. Soil pen­e­tra­bil­ity as a key fac­tor af­fect­ing the nest­ing of bur­row­ing birds. Eco­log­i­cal Re­search, 24/2: 453-459.

Hoi, H., C. Hoi, J. Kistofik, A. Darolava. 2002. Re­pro­duc­tive suc­cess de­creases with colony size in the Eu­ro­pean bee-eater. Ethol­ogy Ecol­ogy & Evo­lu­tion, 14: 99-110.

Horváth, G., M. Fis­cher, T. Szekely. 1992. The de­liv­ery of sur­plus prey to the nest by a pair of bee-eaters (Merops api­aster). Ornis Hung, 2: 11-16.

Kossenko, S., C. Fry. 1998. Com­pe­ti­tion and co­ex­is­tence of the Eu­ro­pean Bee-eater Merops api­aster and the Blue-cheeked Bee-eater Merops periscus in Asia. Ibis, 140/1: 2-13.

Krebs, J., M. Avery. 1985. Cen­tral Place For­ag­ing in the Eu­ro­pean Bee-eater, Merops api­aster. Jour­nal of An­i­mal Ecol­ogy, 54/2: 459-472.

Krebs, J., M. Avery. 1984. Chick growth and prey qual­ity in the Eu­ro­pean Bee-eater (Merops api­aster). Oe­colo­gia, 64/3: 363-368.

Les­sells, C., M. Avery, J. Krebs. 1994. Non­ran­dom dis­per­sal of kin: why do Eu­ro­pean bee-eater (Merops api­aster) broth­ers nest close to­gether?. Be­hav­ior Ecol­ogy, 5: 105-113.

Les­sells, C., M. Avery. 1989. Hatch­ing Asyn­chrony in Eu­ro­pean Bee-eaters Merops api­aster. Jour­nal of An­i­mal Ecol­ogy, 58/3: 815-835.

Les­sells, C., G. Oven­den. 1989. Her­i­tabil­ity of Wing Length and Weight in Eu­ro­pean Bee-Eaters (Merops api­aster). The Con­dor, 91/1: 210-214.

Pe­trescu, A., C. Adam. 2001. In­ter­spe­cific Re­la­tions in the Pop­u­la­tions of Merops api­aster L. (Aves: Coraci­iformes) of South­ern Ro­ma­nia. Travaux du Mu­seum Na­tional d' His­toire Na­turelle, 43: 305-322.

White, F., G. Bartholomew, J. Kin­ney. 1978. Phys­i­o­log­i­cal and Eco­log­i­cal Cor­re­lates of Tun­nel Nest­ing in the Eu­ro­pean Bee-Eater, Merops api­aster. Phys­i­o­log­i­cal Zo­ol­ogy, 51/2: 140-154.

Yosef, R., M. Markovets, L. Mitchell, P. Try­janowski. 2006. Body con­di­tion as a de­ter­mi­nant for stopover in bee-eaters (Merops api­aster) on spring mi­gra­tion in the Arava Val­ley, south­ern Is­rael. Jour­nal of Arid En­v­iorn­ments, 64/3: 401-411.