Ontologia
Abeille domestique

Abeille domestique

Apis melliferaLinnaeus, 1758

1 photo · Licences CC (Wikimedia Commons / iNaturalist)Click pour agrandir

Description

L'Abeille européenne, Avette ou Mouche à miel est une abeille à miel originaire d'Europe. Elle est considérée comme semi-domestique. C'est une des abeilles élevées à grande échelle en apiculture pour produire du miel et pour la pollinisation.

Pays · région · aire protégée · écorégion · biome
Chargement du graphe…

Indicateurs du réseau écologique

Comment lire ce graphe

Ce graphe représente les interactions écologiques documentées entre Apis mellifera et d'autres espèces, à partir de la base GloBI (Global Biotic Interactions, agrégation mondiale de la littérature scientifique) — source principale, complétée par d'autres jeux de données d'interactions agrégés par Ontologia. Il faut le comprendre comme une carte du savoir documenté, pas une carte de la réalité écologique exhaustive.

Limites principales

  • Incomplet. La majorité des interactions écologiques en milieu naturel n'ont jamais été publiées. Une espèce sans liens visibles n'est pas isolée — elle est probablement mal étudiée.
  • Biais publication pharmaco-agronomique. La littérature des interactions est polarisée par les enjeux économiques et sanitaires : parasitism / pathogen sur-pondéré sur les mammifères (recherche zoonoses, vecteurs), herbivory sur-pondéré sur les insectes phytophages (entomologie agronomique). À l'inverse, mutualisms, commensalisms et interactions sol/microbiote sont sous-cités. Conseil de lecture : sur les hubs mammifères ou les insectes ravageurs de culture, lire les arêtes parasitism / herbivory dominantes relativement au contexte de littérature, pas comme une mesure d'intensité écologique brute. Détails §10.1.
  • Biaisé vers les espèces étudiées. Quelques espèces (oiseaux communs, abeille mellifère, espèces modèles) concentrent disproportionnellement plus d'interactions documentées. Notre score composite ajoute un malus aux hubs de littérature pour atténuer cette dominance visuelle.
  • Interactions documentées globalement. Toutes les espèces affichées sont observées en France métropolitaine (les observations sont filtrées sur le territoire métropolitain), mais les interactions entre elles proviennent de la littérature scientifique mondiale. Une interaction documentée à l'étranger peut ne pas se réaliser à l'identique sur votre territoire. Le filtre « restreindre à ma commune » tient compte de la co-occurrence spatiale locale mais ne garantit pas l'interaction effective.
  • Sans dimension temporelle. Les variations saisonnières (migration, floraison, cycle de vie) ne sont pas modélisées.
  • Force d'interaction approximative. L'épaisseur des liens reflète le nombre de fois où l'interaction a été rapportée dans la littérature, pas son importance écologique réelle.

Comment nous sélectionnons les espèces affichées

Le graphe affiche au plus 31 nœuds par fiche (1 centre + 15 bulles depth=1 + 15 partenaires depth=2). Le serveur sélectionne intelligemment :

  • Bulles famille créées si une cascade taxonomique existe ou si ≥3 espèces directement documentées partagent une même famille — les espèces sont absorbées dans la bulle (pas de doublon visuel)
  • Espèces individuelles uniquement quand <3 dans une famille (sans cascade) — relations directes documentées
  • Pas d'espèces inférées affichées en doublon — les cascades sont représentées via les bulles famille uniquement
  • Partenaires depth=2 sélectionnés via algo priorité : candidat partagé par ≥2 docs de la famille (food web central) → reliant entre bulles → top sum_obs en dernier recours
  • Sous-types GloBI traduits en français au survol de la flèche (chasse, parasite, parasitoïde, mycorhize…)

Le toggle Profondeur 1 ↔ 2 client-side cache ou affiche les partenaires depth=2 sans refetch. Filtres règne, type d'interaction, ordres/familles, patrimoniales et commune recalculent côté serveur (slow path live ~1-2 s).

Indicateurs avancés (mode expert) : Modularité Q (Newman 2006, PNAS), communautés (Louvain, Blondel et al. 2008, J. Stat. Mech.), nestedness NODF (Almeida-Neto et al. 2008, Oikos).

Source : GloBI · TAXREF v18 (INPN/MNHN) · BDC-Statuts · Wikidata

5 627 partenaires écologiques documentés directement dans GloBI.

Partenaires
5 627
Espèces avec interactions documentées
Types d'interactions
18
Prédation, pollinisation, parasitisme…
Connectance
0.069
Densité des liens dans le sous-graphe affiché
Rang animalia
100 %
Percentile vs ensemble des animalia

Liste rouge IUCN

DD · Données insuffisantesDécroissante
Évaluation complète
Évaluation
2025 · v3.1
Altitude
m
Profondeur
m
État de la populationExpert
A recent study (Kohl and Rutschmann, submitted) synthesised the survival rates of free-living colonies monitored at 698 nest sites in seven European countries (France, Germany, Luxembourg, Poland, Spain, Switzerland, United Kingdom) between 2013–2025, estimating an overall median population decline of 56% over a projected ten-year period. Although additional colonies are being monitored in other countries, such as Ireland (Browne et al. 2020), Serbia (Bila Dubaić et al. 2021), and Italy (Fontana et al. 2023), this survival-rates analysis represents the only synthesis available to date that estimates population decline based on observed survival data. Given the extensive geographical scope of this analysis, covering different types of landscapes and habitats (e.g., forest, semi-natural, agricultural, urban, etc.), this estimate can be considered an indicator of the suspected decline of wild Western Honey Bee populations within countries of the EU27 range, plus Switzerland and southeast England.

At the broader Pan European scale, the estimated decline might be less pronounced as, for instance, understudied regions (e.g., eastern and far eastern European areas) could contain higher quality habitats that better support wild populations (e.g., see Requier et al. 2020). However, we suggest that a decline should be precautionarily considered even at this level, as free-living colonies in these areas are exposed to the same threats as those in the studied regions. Nevertheless, given the lack of survival data on free-living colonies from such regions, for the present assessment, it is not possible to assess a precise conservation status for wild Western Honey Bee populations at that scale.

Menaces identifiées(8 menaces classées CMP-IUCN)

  • 1_1
    Housing & urban areas
    UnknownUnknownOngoing
  • 2_1_4
    Scale Unknown/Unrecorded
    UnknownUnknownOngoing
  • 2_2_3
    Scale Unknown/Unrecorded
    UnknownUnknownOngoing
  • 2_3_4
    Scale Unknown/Unrecorded
    UnknownUnknownOngoing
  • 8_1_2
    Named species
    UnknownUnknownOngoing
  • 8_1_2
    Named species
    UnknownUnknownOngoing
  • 8_1_2
    Named species
    UnknownUnknownOngoing
  • 9_3_3
    Herbicides and pesticides
    UnknownUnknownOngoing
Description complète des menacesExpert
Strong evidence derived from the direct study of free-living colonies or indirectly through investigations on managed ones suggests that unaided colonies face a barrage of threats that can significantly impact their survival in the wild. From these studies, it has been determined that wild, self-sustaining A. mellifera populations in Europe have been greatly impacted and are now considered rare or locally extinct. The primary threats to the survival of wild Honey Bee populations are listed below:

Habitat loss and malnutrition
Intensive land use for agriculture, commercial, and residential development has led to a decrease in the availability of suitable habitats for wild Honey Bee. In particular, one of the major limiting factors is represented by the decrease of forest habitats harbouring large trees capable of hosting cavities suitable for nesting free-living colonies (Requier et al. 2020). Hollow trees situated along tree-lined roads (i.e., avenues) are being removed as part of modernisation efforts and for safety reasons (Oleksa et al. 2013). Moreover, there is generally high competition among species for occupying such cavities, which usually leads to depredation of Honey Bee nests in winter (Kohl et al. 2023).

The lack of floral resources (pollen and nectar) in the environment may impact food reserves and decrease a colony’s survival, especially over winter. Rutschmann et al. (2022) found a positive correlation between the abundance and winter survival of Honey Bee colonies and the proportion of semi-natural habitats (woodland and shrubland) in the surrounding area. This suggests that semi-natural habitats are essential for the survival and conservation of free-living Honey Bees. Therefore, conversion of these habitats for agricultural or other human activities poses a continued threat to wild Honey Bee populations. Maintaining and increasing semi-natural habitats such as woodlands and shrublands could become a viable strategy for conserving free-living Honey Bee populations.

Pathogens, parasites, and predators
Invasive alien species are among the most devastating biotic threats affecting the survival of Honey Bees colonies, both managed and wild.

The ectoparasitic mite Varroa destructor (the Varroa Mite) has been identified as the most likely cause of the demise of wild populations across Europe (Moritz et al. 2007, Jaffé et al. 2010). Varroa was introduced in Europe in the 1960s and rapidly spread across the entire continent and most islands (Traynor et al. 2020). V. destructor affects the health of the western Honey Bee both directly and indirectly. It causes direct damage to developing larvae and pupae by feeding on their fat body, thereby interfering with two fitness components of the Honey Bee: (i) vitality: it lowers immune response and healing mechanisms, as well as alters flying, homing, and orientation abilities in foragers; (ii) reproduction: lowers adults’ weight, causing a reduction in spermatozoids production in males (Noël et al. 2020). Even more severely, it causes indirect damage, serving as a reservoir and vector of several harmful viruses, most notably Deformed Wing Virus (Noël et al. 2020). The few molecular viral surveys carried out on free-living colonies in Europe detected several viruses that are also common in managed colonies. The results are variable, with studies detecting similar, lower, and higher prevalence/loads of different viruses in free-living compared to managed colonies (Thompson et al. 2014, Kohl et al. 2022).

The fungal pathogen Nosema ceranae (Nosema disease) was first documented infecting the Honey Bee in Europe in 2004 (Higes et al. 2006), but it is possible that it arrived earlier. It has been detected in managed colonies all over Europe and has also spread to free-living colonies (Thompson et al. 2014, Łopieńska-Biernat et al. 2017). N. ceranae infects honey bees’ midgut cells and consumes their contents via phagocytosis. It can reduce Honey Bee’ fitness by (i) decreasing lifespan and nursing ability, (ii) inducing precocious foraging, and (iii) affecting olfactory learning, memory, and flight. All these effects can reduce colony size, honey reserves, and brood-rearing capacity, eventually leading to colony demise. N. ceranae seems to cause more harm to colonies in the warmer Mediterranean regions than in the colder climates of northern Europe (Martín-Hernández et al. 2018).

The Honey Bee predator, the Asian Hornet (Vespa velutina), was first sighted in Europe in southwestern France in 2004, and has since expanded across Western Europe, from southern Portugal to the Netherlands and across the English Channel into Great Britain. It is also spreading eastwards to Italy (see the dynamic map at frelonasiatique.mnhn.fr). In this vast non-native area, the Asian Hornet is causing substantial colony losses in managed apiaries, and it is also likely impacting free-living colonies, as it frequently nests in forest habitats. It feeds on many insects but intensifies its predation on Honey Bees from the end of summer to the winter (Requier et al. 2019). In addition to predation, another deleterious impact on colonies occurs in the autumn, when hundreds of hornets hover at the entrance of a colony, disrupting foraging and, thus, interfering with the colony’s winter preparations and sometimes causing starvation (Laurino et al. 2019, Requier et al. 2019).

The Small Hive Beetle (Aethina tumida) is an invasive species that infests Honey Bee colonies and causes the collapse of wax combs and destruction of honey stores, as a result of uncontrolled reproduction inside the nest (Neumann et al. 2016). It was first sighted in Europe in 2014, in managed colonies in the province of Reggio Calabria, Italy. There were also outbreaks in eastern Sicily in 2014 and 2019. Although eradication has not been achieved, restrictive measures have prevented its spread throughout Europe (Mutinelli et al. 2014). Currently, the species is confined to a limited area in Calabria (Federico et al. 2025).

Lastly, the invasive ectoparasitic mite (Tropilaelaps mercedesae), a novel and devastating pest for Western Honey Bee, has recently been reported in managed colonies in Europe (Brandorf et al. 2024, Janashia et al. 2024). Infestation by this mite can lead to drastic losses, as it feeds on brood and can transmit bee viruses (Chantawannakul et al. 2018). Given its successful spread among managed colonies, the mite is expected to be able to infest free-living colonies too, as in the case of Varroa. Its further spread will therefore represent a significant factor limiting the survival of wild Honey Bees in Europe.

Possible effects of beekeeping practices
Some modern beekeeping practices could impact wild A. mellifera populations (Panziera et al. 2022), including: the commercial trade in queens (leading to introgression and threatening the genetic integrity of native populations and subspecies) as well as migratory beekeeping and large-scale selective breeding (which can contribute to the loss of genetic diversity, rendering the species more vulnerable to diseases and environmental changes) (De la Rúa et al. 2009, Pinto et al. 2014, López-Uribe et al. 2017, Requier et al. 2019, Espregueira Themudo et al. 2020, Tanasković et al. 2021, Martínez-López et al. 2022).

The international trade of queens and long-distance migratory beekeeping, the extent of which has increased dramatically over the last century, have promoted the spread of non-local Honey Bee subspecies and those produced through the artificial crossing of multiple subspecies. These practices favour the use and persistence of less viable and locally unsuitable genotypes (Büchler et al. 2014, Meixner et al. 2015, Fontana et al. 2018). Given that Honey Bee mating cannot be fully controlled by beekeepers, and considering the high density of managed colonies in Europe, such maladapted genotypes are likely to have already been introduced into free-living populations, thereby impacting their gene pools and ultimately their survival.

Pesticides, herbicides, and fungicides
Pesticides, herbicides, and fungicides may detrimentally impact the forage availability of A. mellifera (Henry et al. 2012, Prado et al. 2019, Barascou et al. 2022) as well as Honey Bee health (Blacquière et al. 2012). So far, no specific study has been carried out on the effects of exposure of free-living colonies to pesticides. However, colonies nesting in intensive agricultural areas, where these compounds are intensively used, were found to have lower winter survival rates than colonies in semi-natural areas (Rutschmann et al. 2022).

Habitats préférentiels (classification IUCN)

  • 13_3Marine Coastal/Supratidal - Coastal Sand Dunes
  • 14_1Artificial/Terrestrial - Arable Land
  • 14_2Artificial/Terrestrial - Pastureland
  • 14_3Artificial/Terrestrial - Plantations
  • 14_5Artificial/Terrestrial - Urban Areas
  • 1_1Forest - Boreal
  • 1_4Forest - Temperate
  • 3_3Shrubland - Boreal
  • 3_4Shrubland - Temperate
  • 3_8Shrubland - Mediterranean-type Shrubby Vegetation
  • 4_4Grassland - Temperate
  • 5_3Wetlands (inland) - Shrub Dominated Wetlands

+ 2 habitats supplémentaires

Mesures de conservation recommandéesExpert
Further research on free-living colonies is urgently needed in order to identify self-sustaining populations and to understand the status of populations across the whole Pan European level, focusing on data-poor parts, such as the far Eastern regions. This could be achieved through population ecology studies based on repeated genotyping of colonies and long-term monitoring of their nests to infer demographic parameters at the population level (e.g., Kohl et al. 2022, Moro et al. 2024). Furthermore, research should also focus on gaining a more profound comprehension of the threats impacting such populations. Given the present research gap, acquiring such data is essential and will play a pivotal role in facilitating conservation efforts, potentially driving reforms in both national and international policies (Panziera et al. 2022).

Notably, this research could begin (or continue) by monitoring, sampling, and testing the nest locations gathered for this present assessment (see map produced within this report). Additionally, researchers and citizen scientists can contribute data to Honey Bee Watch and/or to the various initiatives that collected these data points (see below).

In response to the urgent need for data on free-living colonies, an international coalition of researchers and stakeholders focused on free-living Honey Bees was established in 2019 to locate, monitor, study, and protect wild A. mellifera populations. Honey Bee Watch‘s mission is to create an extensive repository of data, protocols, and resources pertaining to free-living colonies, which will be used to empower further research and enable conservation endeavours.

For this reassessment, HBW acknowledges the contributions of numerous partners involved in the study of free-living Honey Bee colonies in Europe, who, along with other initiatives, shared data for building a map of confirmed sightings of free-living colonies in Europe (see Geographic Range section):
  • BEEtree-Monitor, Germany
  • Blenheim Palace and Estate, United Kingdom
  • Boomtreebees, Ireland
  • Boughton Estate Honeybee Conservation Project, United Kingdom
  • Edmund Mach Foundation, Italy
  • Galway Honey Bee Research Centre, University of Galway, Ireland
  • Honey Bee Wild, Luxembourg
  • Honungsbiföreningen, Sweden
  • Instituto Politécnico de Bragança, Portugal
  • Kazimierz Wielki University, Poland
  • Nature Research Centre, Lithuania
  • Office pour les insectes et leur environnement (OPIE), France
  • Resilient Bee Project, Italy
  • Slovak University of Agriculture in Nitra, Slovakia
  • UMR CNRS-IRD-Université Paris-Saclay, France

  • University of Belgrade, Serbia
  • University of Sussex, United Kingdom
  • University of Würzburg, Germany
  • Wild Bees Project, France
In addition to the groups listed above, other initiatives are also surveying and/or monitoring free-living colonies in Europe (e.g., FreeTheBees, Swiss BeeMapping, Dortmund free-living colonies study, etc.), but were not able to or chose not to share data for this reassessment due to a variety of reasons.

Immediate measures considered beneficial for the preservation of wild A. mellifera populations include (i) ensuring the conservation of natural habitats rich in suitable nesting cavities (Oleksa et al. 2013, Kohl and Rutschmann 2018, Requier et al. 2020, Rutschmann et al. 2022), (ii) controlling the spread of invasive Honey Bee predators and parasites, and (iii) promoting the use of native and regional subspecies for beekeeping to avoid non-native genotypes introgression in local wild subpopulations. The latter recommendation is particularly promoted by the International Association for the Protection of the European Dark Bee (SICAMM), the Native Irish Honey Bee Society (NIHBS), and have been endorsed in Italy through the San Michele All’Adige and the Pantelleria declarations (Fontana et al. 2018, 2022), as well as by the Berlin Declaration on Wild Western Honey Bee Conservation in Europe. National-level strategies in line with these objectives also include the legal restriction on the importation of queens of non-native subspecies, which are already active in Serbia, Slovenia, and the Canary Islands, and under consideration in Ireland.
Stress écologiques (17)Expert
  • 1_1Ecosystem conversion
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_2Ecosystem degradation
  • 1_3Indirect ecosystem effects
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_1Species mortality
  • 2_2Species disturbance
  • 2_3_7Reduced reproductive success
  • 2_3_7Reduced reproductive success
Usage & commerce (1)Expert
  • 17Other (free text)
    national
Niche IUCN globaleExpert

Royaumes biogéographiques

Palearctic

Systèmes (terrestre/eau douce/marin)

Terrestrial
Références bibliographiques (30)Expert
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  2. Rutschmann, B., Kohl, P.L. and Steffan-Dewenter, I. 2025. Swarming rate and timing of unmanaged honeybee colonies (<i>Apis mellifera carnica</i>) in a forest environment. <i>Insectes Sociaux</i>: https://doi.org/10.1007/s00040-025-01028-y
  3. Brandorf, A., Ivoilova, M.M., Yañez, O., Neumann, P. and Soroker, V. 2025. First report of established mite populations, <i>Tropilaelaps mercedesae</i>, in Europe. <i> Journal of Apicultural Research</i> 64(3): 842–844. https://doi.org/10.1080/00218839.2024.2343976
  4. Rutschmann, B., Remter, F. and Roth, S. 2025. Monitoring Free-Living Honeybee Colonies in Germany: Insights Into Habitat Preferences, Survival Rates, and Citizen Science Reliability. <i>Ecology and Evolution</i> 15(6): e71469. https://doi.org/10.1002/ece3.71469
  5. Federico, G., Mutinelli, F., Formato, G., Ponti, A.M., Bertola, M. and Neumann, P. 2025. Ten years of containing small hive beetles in Southern Italy. <i>Management of Biological Invasions</i> 16(2): 563–580, https://doi.org/10.3391/mbi.2025.16.2.14
  6. Janashia, I., Uzunov, A., Chen, C., Costa, C. and Cilia, G. 2024. First Report on <i>Tropilaelaps mercedesae</i> Presence in Georgia: The Mite is Heading Westward! <i>Journal of Apicultural Science</i> 68(2): 183–188.
  7. Moro, A., Albouy, V., Dickey, M., Kohl, P.L., McCormack, G.P., Remter, F., Requier, F., Rogenstein, S., Rutschmann, B., Thiele, M.J., Visick, O. and Bila Dubaić, J. 2024. A Protocol for Monitoring Populations of Free-Living Western Honey Bees in Temperate Regions. <i>Bee World</i> 101(3-4): 1-5. https://doi.org/10.1080/0005772X.2024.2402109
  8. Kohl, P.L., Rutschmann, B., Sikora, L.G., Wimmer, N., Zahner, V., D’Alvise, P., Hasselmann, M. and Steffan-Dewenter, I. 2023. Parasites, depredators, and limited resources as potential drivers of winter mortality of feral honeybee colonies in German forests. <i>Oecologia</i> 202(3): 465–480.
  9. Fontana, P., Andreis, D., Corradini, S., <i>et al</i>. 2023. Mapping and monitoring western honey bee unmanaged colonies. <i>Naturalista siciliano</i> 46(1): 105-108.
  10. Rutschmann, B., Kohl, P.L. and Steffan-Dewenter, I. 2023. Foraging distances, habitat preferences and seasonal colony performance of honeybees in Central European forest landscapes. <i>Journal of Applied Ecology</i> 60: 1056–1066.
  11. Visick, O.D. and Ratnieks, F.L.W. 2023. Ancient, veteran and other listed trees as nest sites for wild-living honey bee, <i>Apis mellifera</i>, colonies. <i>Journal of Insect Conservation</i> 28: 153-163. https://doi.org/10.1007/s10841-023-00530-7
  12. Fontana P., Lo Verde G., Malagnini V. 2023. Proceedings of the First international meeting APIS SILVATICA, The Western honey bee in nature (Pantelleria, Italy, May 16-20, 2022. Il Naturalista siciliano, S. IV, XLVI (1): 255 pp..
  13. Barascou, L., Sene, D., Le Conte, Y. and Alaux, C. 2022. Pesticide risk assessment: honeybee workers are not all equal regarding the risk posed by exposure to pesticides. <i>Environmental Science and Pollution Research</i> 29(60): 90328-90337. https://doi.org/10.1007/s11356-022-21969-2
  14. Kohl, P.L., Rutschmann, B. and Steffan-Dewenter, I. 2022. Population demography of feral honeybee colonies in central European forests. <i>Royal Society Open Science</i> 9(8): 220565. https://doi.org/10.1098/rsos.220565
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  17. Panziera, D., Requier, F., Chantawannakul, P., Pirk, C.W.W. and Blacquière, T. 2022. The Diversity Decline in Wild and Managed Honey Bee Populations Urges for an Integrated Conservation Approach. <i>Frontiers in Ecology and Evolution</i> 10: 767950. https://doi.org/10.3389/fevo.2022.767950
  18. Martínez-López, V., Ruiz, C. and De la Rúa, P. 2022. Migratory beekeeping and its influence on the prevalence and dispersal of pathogens to managed and wild bees. <i>International Journal for Parasitology: Parasites and Wildlife</i> 18: 184-193.
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  23. Requier, F., Paillet, Y., Laroche, F., Rutschmann, B., Zhang, J., Lombardi, F., Svoboda, M. and Steffan‐Dewenter, I. 2020. Contribution of European forests to safeguard wild honeybee populations. <i>Conservation Letters</i> 13(2): 12693. https://doi.org/10.1111/conl.12693
  24. Espregueira Themudo, G., Rey-Iglesia, A., Robles Tascón, L., Bruun Jensen, A., da Fonseca, R.R. and Campos, P.F. 2020. Declining genetic diversity of European honeybees along the twentieth century. <i>Scientific Reports</i> 10(1): 10520.
  25. Noël, A., Le Conte, Y. and Mondet, F. 2020. <i>Varroa destructor</i>: How does it harm <i>Apis mellifera</i> honey bees and what can be done about it? <i>Emerging Topics in Life Sciences</i> 4(1): 45–57. https://doi.org/10.1042/ETLS20190125
  26. Browne, K.A., Hassett, J., Geary, M., Moore, E., Henriques, D., Soland-Reckeweg, G., Ferrari, R., Mac Loughlin, E., O’Brien, E., O’Driscoll, S., Young, P., Pinto, M.A. and McCormack, G.P. 2020. Investigation of free-living honey bee colonies in Ireland. <i>Journal of Apicultural Research</i> 60(2): 1-12. https://doi.org/10.1080/00218839.2020.1837530
  27. Groeneveld, L.F., Kirkerud, L.A., Dahle, B., Sunding, M., Flobakk, M., Kjos, M., Henriques, D., Pinto, M.A. and Berg, P. 2020. Conservation of the dark bee (<i>Apis mellifera mellifera</i>): Estimating C-lineage introgression in Nordic breeding stocks. <i>Acta Agriculturae Scandinavica, Section A — Animal Science</i> 69(3): 157–168.
  28. Traynor, K.S., Mondet, F., de Miranda, J.R., Techer, M., Kowallik, V., Oddie, M.A.Y., Chantawannakul, P. and McAfee, A. 2020. <i>Varroa destructor</i>: A complex parasite, crippling honey bees worldwide. <i>Trends in Parasitology</i> 36(7): 592–606.
  29. Requier, F., Rome, Q., Chiron, G., Decante, D., Marion, S., Ménard, M., Muller, F., Villemant, C. and Henry, M. 2019. Predation of the invasive Asian hornet-induced risk on honeybee colony collapse affects foraging activity and survival probability of honey bees in Western Europe. <i>Journal of Pest Science</i> 92(2): (2567-578. https://doi.org/10.1007/s10340-018-1063-0
  30. Requier, F., Garnery, L., Kohl, P.L., Njovu, H.K., Pirk, C.W.W., Crewe, R.M. and Steffan-Dewenter, I. 2019. The Conservation of Native Honey Bees Is Crucial. <i>Trends in Ecology & Evolution</i> 34(9): 789–798.
Évaluateurs & contributeurs (3)Expert
assessor
Moro, A., Kohl, P., Rutschmann, B., Bila Dubaić, J., Browne, K.A., Pinto, M.A., Requier, F., Rogenstein, S., Dall'Olio, R., Oleksa, A., De la Rúa, P., McCormack, G., Fontana, P. & Kryger, P.
contributor
Albouy, V., Blažytė-Čereškienė, L., Bonhoff, H., Cliceri, D., Dammé, R., Ibbertson, J., Licón Luna, R.M., Malagnini, V., Park, J., Pavle, M., Remter, F., Roth, S., Salbany, F., Valentine, A., Valentini, A., Verspuij, M. & Visick, O.
evaluator
Michez, D. & Put, S.

Moro, A., Kohl, P., Rutschmann, B., Bila Dubaić, J., Browne, K.A., Pinto, M.A., Requier, F., Rogenstein, S., Dall'Olio, R., Oleksa, A., De la Rúa, P., McCormack, G., Fontana, P. & Kryger, P. 2025. Apis mellifera (Europe assessment). The IUCN Red List of Threatened Species 2025: e.T42463639A277757621. Accessed on 05 May 2026.

Traits biologiques

3 valeurs · 5 sources

Morphologie(2)

Masse adulte
84 mg
AnimalTraits
Masse cerveau
1 mg
AnimalTraits

Cycle de vie(1)

Longévité max
8 ans
AnAge

Sources priorisées par qualité scientifique (peer-reviewed spécialisées → Wikidata fallback). Unités auto-converties, valeur max retenue en cas de mesures multiples. Méthodologie · Citations.

Répartition mondiale (heatmap GBIF)

1 055 446 obs · 32 972 cellules · 15742026
Densité obs.
≥ 485
43–484
9–42
3–8
< 3

Source : GBIF — observations agrégées par hexagones 0.2° × 0.2° (~22km). Filtre qualité : précision coordonnée < 10 km. Coloration quantile (q50/70/90/99). Fond carte : OpenFreeMap · © OpenStreetMap.

Distribution mondiale

227 pays · 1 083 375 obs.
+ 217 autres pays
Zoom régions (top 50)
Poland
United States
United Kingdom
Germany
Netherlands

Source : GBIF — observations géoréférencées agrégées par administration GADM (pays + région). Compléments dans la section Aires de répartition ci-dessous (Catalogue of Life).

Phénologie

1 086 315 obs. datées / 1 092 035 total
6%
J
6%
F
8%
M
12%
A
10%
M
13%
J
13%
J
12%
A
9%
S
6%
O
2%
N
4%
D

Source : GBIF — observations agrégées par mois (date d'événement). Phénologie globale (toutes localisations confondues).

Aires de répartition

9 régions · Source Catalogue of Life
  • Africa
  • Australia
  • Caribbean
  • Europe & Northern Asia (excluding China)
  • Middle America
  • North America
  • Oceania
  • South America
  • Southern Asia

Régions biogéographiques selon la classification CoL (Catalogue of Life). Granularité grossière (sub-continents) — la carte choroplèthe par administration sera disponible avec le calcul matview depuis GBIF.

Consulter sur les bases externes

Observations & statuts

Cartographie

Bibliographie

Note nomenclaturale & synonymesExpert

Note nomenclaturale

TAXREF v18 — INPN/MNHN

Synonymes (50)— redirigent vers cette page

  • Apis adansoniiLatreille, 1804
  • Apis aenigmaticusRayment, 1925
  • Apis australisKiesenwetter, 1860
  • Apis caffraLepeletier, 1836
  • Apis ceriferaScopoli, 1770
  • Apis ceriferaGerstäcker, 1862
  • Apis dauricaFischer von Waldheim, 1843
  • Apis gregariaGeoffroy, 1762
  • Apis intermissaMaa, 1953
  • Apis mellica cypriaPollmann, 1879
  • Apis mellica remipesGerstäcker, 1862
  • Apis mellida caucasiaPollmann, 1889
  • Apis mellifera acervorumSkorikov, 1929
  • Apis mellifera adamiRuttner, 1975
  • Apis mellifera adansoniLatreille, 1804
  • Apis mellifera anatoliacaMaa, 1953
  • Apis mellifera armeniacaSkorikov, 1929
  • Apis mellifera artemisiaEngel, 1999
  • Apis mellifera capensisEschscholtz, 1822
  • Apis mellifera carnicaPollmann, 1879
  • Apis mellifera carniolicaKoschevnikov, 1900
  • Apis mellifera carpaticaBarac, 1977
  • Apis mellifera caucasicaGorbachev, 1916
  • Apis mellifera cecropiaKiesenwetter, 1860
  • Apis mellifera cypriaPollmann, 1879
  • Apis mellifera ibericaRuttner, 1988
  • Apis mellifera iberiensisEngel, 1999
  • Apis mellifera intermissaMaa, 1953
  • Apis mellifera jemeniticaRuttner, 1976
  • Apis mellifera lamarckiiCockerell, 1906
  • Apis mellifera ligusticaSpinola, 1806
  • Apis mellifera litoreaF. G. Smith, 1961
  • Apis mellifera macedonicaRuttner, 1988
  • Apis mellifera majorRuttner, 1976
  • Apis mellifera medaSkorikov, 1929
  • Apis mellifera monticolaF. G. Smith, 1961
  • Apis mellifera nubicaRuttner, 1976
  • Apis mellifera remipesGerstäcker, 1862
  • Apis mellifera ruttneriSheppard, Arias, Grech & Meixner, 1998
  • Apis mellifera sahariensisBaldensperger, 1932
  • Apis mellifera scutellataLepeletier, 1836
  • Apis mellifera sicilianaGrassi, 1881
  • Apis mellifera siculaMontagano, 1911
  • Apis mellifera simensisMeixner, Leta, Koeniger & Fuchs, 2011
  • Apis mellifera sossimaiEngel, 1999
  • Apis mellifera syriacaSkorikov, 1929
  • Apis mellifera tauricaAlpatov, 1935
  • Apis mellifera unicolorLatreille, 1804
  • Apis mellificaLinnaeus, 1761
  • Apis mellifica adamiRuttner, 1975

Sources : Catalogue of Life Cross-References (synonymes) · TAXREF v18 INPN/MNHN (commentaires FR).