Anthidium manicatum

Anthidium manicatum, commonly called the European wool carder bee[1] is a species of bee in the family Megachilidae, the leaf-cutter bees or mason bees.[2]

Anthidium manicatum
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Megachilidae
Genus: Anthidium
Species:
A. manicatum
Binomial name
Anthidium manicatum
Synonyms
See text

They get the name "carder" from their behaviour of scraping hair from leaves[3] such as lamb's ears (Stachys byzantina). They carry this hair bundled beneath their bodies to be used as a nest lining.[4] Like other members of the tribe Anthidiini, these bees do not cut leaves or petals as is typical for megachilids.[5] The males engage in territorial behaviour, aggressively chasing other males and pollinators from their territory.[6]

This bee is native to Europe, Asia and North Africa. It has recently been seen in regions of South America, New Zealand, and the Canary Islands. They are generalists, and do not seem to prefer any plant genera for foraging, although in New Zealand native plants are visited less frequently by this bee species.

It was accidentally introduced into North America from Europe some time in the mid 20th century, first seen in 1963 near Ithaca, New York, and since then an invasive pest.[6]

Taxonomy and phylogeny

This species belongs to the family Megachilidae and the order Hymenoptera, which consists of organisms such as ants, bees and wasps, and the superfamily Apoidea, which is more specific to bees and wasps.[7]

Description and identification
Detail of patterns on the abdomen of a male Anthidium manicatum
A female A. manicatum
A male A. manicatum

Anthidium manicatum is originally an Old World bee. It has a wingspan of approximately 20 millimetres (0.79 in), with a body length of about 11–13 mm (0.43–0.51 in) for females, and 14–17 mm (0.55–0.67 in) for males.[8] The males are substantially larger than females.[1]

A. manicatum are black and covered with yellow-grey hairs. Their faces and abdomen are covered in yellow spots. Male A. manicatum have a black head and thorax, coated with short yellowish brown hairs. The cheeks below the antennae, a small spot behind each eye, a bilobate spot on the clypeus, and the mandibles (except the apex) are yellow. The wings are dusky in color. The abdomen is black with grey hairs, with a band of brown hairs at each segment's apex as well as along their lateral margins.[9] This feature distinguishes male A. manicatum from New World Anthidium species.[10] There is a yellow spot on each side of the segments except the 7th. A second pair of spots is often seen on the disks of the 4th and 5th segments. There is a spine on each side of the 6th and 7th segments at the apex, the 7th having a third thin spine in the middle. The legs exhibit variegation of yellow and are covered with grey hairs. Female A. manicatum are smaller in size than the males, but have a similar color pattern. The abdominal spots are smaller and the apex is rounded. Female legs are almost completely black, with very small yellow spots.[9] The anterior sides of the tarsal segments of each leg of female A. manicatum have fine, soft and small white-colored hairs. This pilosity occurs in most species of Anthidium in the Western Palearctic region.[11]

Male A. manicatum resemble A. maculosum in appearance. The two species have similar spiniform pygidia, as well as largely rounded sixth sterna (although that of A. manicatum is more so).[10]

Distribution and habitat

Anthidium manicatum is found in parts of Europe, Asia, North Africa, and North America. It has also recently been documented in the Canary Islands, and South American countries such as Argentina, Brazil, Paraguay, and Uruguay.[12][13] As of 2006, this species is also now established in New Zealand.[14]

This insect was accidentally introduced into the United States from Europe sometime prior to 1963, when it was discovered in New York State.[15] It has since spread from the northeastern U.S. and southeastern Canada across the United States to California, where it was first collected in 2007.[16] This species' tendency to occupy ready-made nesting sites, usually movable objects, allows it to spread to new locations easily.[10]

In Europe, this species is normally found in gardens, fields, and meadows in the southern part of Wales and England, but is localized in other places within the United Kingdom,[4] where they can be seen from May to September.[4] A. manicatum is the only species of the genus Anthidium that can be found in England.[17]

Nesting
'Wooly' trichomes as seen on Stachys byzantina, used by A. manicatum for nest construction.

Being a member of the Anthidiini tribe of megachilid bees, A. manicatum engages in highly elaborate nesting behavior. These bees construct their nests in preexisting cavities, using the trichomes of wooly plants. Female A. manicatum use their mandibles, which are sharply toothed, to remove trichomes from the stems and leaves of various plants. They then roll up the trichomes into a ball and bring them to a preexisting cavity. Inside the cavity, the bees fashion the trichome ball into cells, where they deposit an egg as well as a provisioning mass consisting of nectar and pollen. The female creates several cells in a cavity. Once finished, she seals the entrance to the cavity with a terminal plug, which consists of inorganic and organic materials that she brings to the nest.[18]

Females collect "down" from such plants as lamb's ears (Stachys byzantina). They scrape the hairs from the leaves and carry them back to their nests bundled beneath their bodies. There it is used as a lining for their nest cavities.[1][19]

Females tend to build their nests at high locations. This may be in order to minimize the nest's exposure to parasites and predators. This may also be to avoid nest usurpation by other female A. manicatum.[18]

Materials

Besides trichomes, other materials used by female A. manicatum for building brood cells include mud, stones, resin, and leaves. Some of the plant materials that are collected are hydrophobic, a feature that may serve an anti-microbial function for the nest. Females smear a plant substrate, plant extrafloral trichome secretions, on brood cells. The primary material used to build the cells are plant hairs, or "wool" (hence the name "wool carder bee"), that is collected from the stems and leaves of plants. Females largely use the hairs of Lamiaceae, especially those of the genus Betonica or Stachys. Additionally, females use specialized hair-like structures on the exterior of their tarsi to absorb the secretions of the plant hairs to apply onto the brood cells. These secretions are obtained from different species, such as Anthirrinum, Crepis, and Pelargonium.[20]

Behavior
Anthidium manicatum asleep in a flower

Mating behavior

The mating system of A. manicatum is unlike those of most other bees. Females exhibit polyandry and continuously mate throughout their reproductive life.[21] The interval of time between copulations amongst different males can be as short as 35 seconds in length.[22] Males exhibit resource defense polygyny. A. manicatum display extreme polyandry, which is linked to male territoriality and resource defence of flowering plants. Males claim patches of floral plants, aggressively ward off conspecific males, bees, and other resource competitors, and mate with the females who forage in their territories. Copulations occur repeatedly and regularly in both sexes. Males that are unable to defend their own territory (usually because of their relatively small size) utilize an alternative ‘sneaking’ tactic. These unfit males receive fewer copulation opportunities than females.[21]

Such mating and territorial behaviour in bees has also been observed in Anthidiellum notatum, Anthidiellum perplexum, and Anthidium banningense. However, males of the genus Anthidiellum chase away intruders rather than physically attacking them, so their aggressive behaviour differs significantly.[23]

Resource defence and aggression

The territorial mating behaviour of male A. manicatum occurs when foraging resources are amassed, allowing for monopolization and defence of territories by individual males.[21] Resource defence, as exhibited by male A. manicatum, has been thought to benefit females by reducing foraging competition for pollen and nectar.[21] The rate a female visits a territory is highly correlated with the number of flowers in that area.[22] If females forage in sites that are being defended by males and the cost of additional matings is low for female members, then male resource defence and female polyandry may co-evolve.[21]

Male A. manicatum display highly aggressive behaviour.[24] Males are highly aggressive towards each other as well as other visitors to the flowers in its territory.[1] In the process of obtaining and defending flowering plant territories, males will regularly patrol their territory and attack conspecific males and heterospecific pollinators. This typically consists of brief aggressive "tackles" but they will sometimes lethally injure the pollinators as a result of their aggressiveness.[18] The territorial behaviour of males develops after a period of flight without any localisation in search of a suitable flower patch.[24] They will also defend conspecific females,[13] although they do harass them by holding them immobile and repeatedly attempting to mate.[2]

Late male sperm precedence

Studies show that there appears to be no selection pressure on male A. manicatum to be the first to copulate, and hence no (or very little) selection pressure to emerge before females.[25] This is due to the females' polyandrous behaviour, and can also be attributed to a phenomenon called "'Late' male sperm precedence".

Patterns of sperm use by the females determine the benefits of resource defence for males. If the female uses only the sperm from her first copulation in a breeding season, then selection will not favor the ‘sit-and-wait’ strategy of resource defence for the males over strategies that are pre-emptive, such as patrolling nest sites. However, if delayed mating can still ensure a high probability of procreating, then the resource defence strategy will be favoured.[21]

‘Late male sperm precedence’, or LMSP, is an experimental situation in which two males mate in sequence with a female and the second male will hold paternity of over 50% of the female's offspring. Although females do have a spermatheca for long-term sperm storage, more recent mates tend to father the brood she produces. This phenomenon might be caused by a variety of mechanisms, including sperm digestion or removal by the female, removal by the next male, or stratification of sperm from different males in the sperm storage organ of the female (i.e. the last sperm in is the first to come out). Studies have shown that A. manicatum males that copulate late in a sequence have a greater than average chance of paternity of the female's eggs. Late male sperm precedence may have fostered the evolution of resource defence in A. manicatum males.[21]

Diet and foraging behavior

Anthidium manicatum consumes the pollen from flowers of varying families. They are thus considered to be generalists. They visit garden flowers and weeds preferring blue flowers that have long throats[1] with Old World origins.[1] Both males and females can maintain a precise static hover near flowers similar to flies in the family Syrphidae.[26]

Sexual dimorphism

Unlike most other species of Hymenoptera, male A. manicatum are larger than females in size, displays male-biased sexual dimorphism. The selection for larger size in males may have resulted due to their aggressive territorial behavior and subsequent differential mating success. Although it does not tear other males apart, the abdominal armature of a male A. manicatum may have been developed due to territorial aggression, rather than for mating purposes.[24] Male size has been found to correlate with mating success. Smaller males will implement alternative mating tactics if they cannot defeat larger males for territory.[18]

The mating behavior of male A. manicatum can be determined by relative body size to other conspecific males. Territory owners are larger in size than wanderers, and copulate with females more frequently as well. The number of copulations a male territory owner can achieve varies based on the size of the territory – males with larger territories generally achieve more copulations than those with smaller territories. This difference may be due to the energy expenditure of smaller bees to defend their territory from larger males, the inability of small males to mate on their territory, or female choice of larger males (regardless of territory size).[27] Hence the number of copulations a male obtains is positively correlated with territory quality as well as male size.[21]

Subspecies

  • Anthidium manicatum manicatum (Linnaeus, 1758)
  • Anthidium manicatum barbarum Lepeletier, 1841
  • Anthidium manicatum gribodoi Schwarz and Gusenleitner, 2003

Synonyms

  • Apis manicata Linnaeus, 1758
  • Apis pervigil Harris, 1776
  • Apis maculata Fabricius, 1781
  • Apis fulvipes de Villers, 1789 (homonym)
  • Apis modesta Christ, 1791
  • Apis amoenita Christ, 1791
  • Apis uncata Schrank, 1802
  • Anthidium maculatum Latreille, 1806 (homonym)
  • Anthidium marginatum Latreille, 1809
  • Anthidium obtusatum Lepeletier, 1841
  • Anthidium productum Lepeletier, 1841
  • Anthidium manicatum var. nigrithorax Dalla Torre, 1877
  • Anthidium manicatum var. fasciatum Schirmer, 1915
  • Anthidium manicatum var. nasicolle Friese, 1917
  • Anthidium manicatum var. luteus Gribodo, 1924 (homonym)
  • Anthidium manicatum subcrenulata Alfken, 1930
  • Anthidium manicatum cyrenaica van der Zanden, 1992 (homonym)

See also

References
  1. Species Anthidium manicatum – European Wool Carder Bee – BugGuide.Net
  2. Wool Carder Bee / Leafcutting Bee – Anthidium manicatum
  3. Anthidium manicatum – Wool Carder Bee Archived July 28, 2010, at the Wayback Machine, Bees, Wasps & Ants Recording Society
  4. Wool Carder Bees – Anthidium manicatum – UK Safari
  5. Michener, C.D. (2000). The Bees of the World. Johns Hopkins University Press. 913 pp.
  6. Graham, Kelsey K. "Bee battles: why our native pollinators are losing the war". The Conversation. Retrieved 10 July 2020. The European wool-carder bee was first discovered in North America in 1963 near Ithaca, New York, and since then, its impact has been felt from coast to coast.
  7. "Anthidium Manicatum". Integrated Taxonomic Information System on-line database. Retrieved 14 October 2015.
  8. Anthidium manicatum (Linnaeus, 1758), Discover Life
  9. Saunders, Edward (1884). The Transactions of the Entomological Society of London for the Year 1884. The Society., 1884. p. 218.
  10. Jaycox, Elbert R. (January 1967). "An Adventive Anthidium in New York State (Hymenoptera: Megachilidae)". Journal of the Kansas Entomological Society. 40 (1): 124–126. JSTOR 25083603.
  11. Müller, A.; Töpfl, W.; Amiet, F. (1996). "Collection of Extrafloral Trichome Secretions for Nest Wool Impregnation in the Solitary Bee Anthidium manicatum". Naturwissenschaften. 83 (5): 230–232. Bibcode:1996NW.....83..230M. doi:10.1007/BF01143331.
  12. "Anthidium manicatum (Linnaeus, 1758)". Moure's Bee Catalogue. Archived from the original on 11 June 2016. Retrieved 6 May 2016.
  13. L. L. Pechuman (1967). "Observations on the behavior of the bee Anthidium manicatum (L.)". Journal of the New York Entomological Society. 75 (2): 68–73. JSTOR 25006048.
  14. Apoidea (Insecta: Hymenoptera). Fauna of New Zealand 57.
  15. "Archived copy". Archived from the original on 2011-07-18. Retrieved 2011-01-29.CS1 maint: archived copy as title (link)
  16. Anthidium manicatum – Definition and Scientific Information – Page 1
  17. Pechuman, L. L. (June 1967). "Observations on the Behavior of the Bee Anthidium manicatum (L.)". Journal of the New York Entomological Society. 75 (2): 68–73. JSTOR 25006048.
  18. Payne, Ansel; Schildroth, Dustin A.; Starks, Philip T. (12 May 2010). "Nest site selection in the European wool-carder bee, Anthidium manicatum, with methods for an emerging model species" (PDF). Apidologie. 42 (2): 181–191. doi:10.1051/apido/2010050. Archived from the original (PDF) on 6 November 2015. Retrieved 10 October 2015.
  19. Anthidium manicatum – Wool Carder Bee Archived July 28, 2010, at the Wayback Machine
  20. Eltz, Thomas; Küttner, Jennifer; Lunau, Klaus; Tollrian, Ralph (6 January 2015). "Plant secretions prevent wasp parasitism in nests of wool-carder bees, with implications for the diversification of nesting materials in Megachilidae". Frontiers in Ecology and Evolution. 2. doi:10.3389/fevo.2014.00086.
  21. Lampert, Kathrin P.; Pasternak, Vanessa; Brand, Philipp; Tollrian, Ralph; Leese, Florian (9 January 2014). "'Late' male sperm precedence in polyandrous wool-carder bees and the evolution of male resource defence in Hymenoptera" (PDF). Animal Behaviour. 90: 211–217. doi:10.1016/j.anbehav.2014.01.034. Retrieved 9 October 2015.
  22. Severinghaus, Lucia L.; Kurtak, Barbara H.; Eickwort, George C. (27 March 1981). "The Reproductive Behavior of Anthidium manicatum (Hymenoptera: Megachilidae) and the Significance of Size for Territorial Males". Behavioral Ecology and Sociobiology. 9: 51–58. doi:10.1007/BF00299853.
  23. Turell, Michael J. (March 1976). "Observations on the Mating Behavior of Anthidiellum notatum and Anthidiellum perplexum". The Florida Entomologist. 59 (1): 55–61. doi:10.2307/3493170. JSTOR 3493170.
  24. Jaycox, Elbert R. (October 1967). "Territorial Behavior Among Males of Anthidium Bamngense". Journal of the Kansas Entomological Society. 40 (4): 565–570. JSTOR 25083662.
  25. Wirtz, P.; Kopka, S.; Schmoll, G. (1991). "Phenology of two territorial solitary bees, Anthidium manicatum and A. florentinum (Hymenoptera: Megachilidae)". Journal of Zoology. 228 (4): 641–651. doi:10.1111/j.1469-7998.1992.tb04461.x.
  26. "Wool Carder Bee – Anthidium manicatum Family Megachilidae". North American Insects and Spiders. Red Planet, Inc. Retrieved October 22, 2015.
  27. Starks, P. T.; Reeve, H. K. (1999). "Condition-based alternative reproductive tactics in the wool-carder bee, Anthidium manicatum". Ethology Ecology & Evolution. 11: 71–75. doi:10.1080/08927014.1999.9522843.

Further reading
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