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common name: European wool carder bee
scientific name: Anthidium manicatum (Linnaeus) (Insecta: Hymenoptera: Megachilidae)

Introduction - Synonymy - Distribution - Description - Life Cycle and Biology - Hosts - Economic Importance - Selected References

Introduction (Back to Top)

The European wool carder bee Anthidium manicatum (Linnaeus) is a solitary, cavity-nesting bee species in the family Megachilidae (tribe Anthidiini), a family whose members include the mason and leaf cutter bees. Wool carder bees are so named because the female bee scrapes and collects the soft downy hairs (trichomes) of fuzzy plants to use in building a nest for her young. Some consider male wool carder bees very charismatic and enjoy watching them chase after other bees that invade their territory, while others would call them bullies based on male bees’ aggressive tendencies toward other bees when defending floral resources.

This species has been called the most widely distributed unmanaged bee in the world (Strange et al. 2011) because of its expansive native and non-native range.

Adult male European wool carder bee, Anthidium manicatum

Figure 1. Adult male European wool carder bee, Anthidium manicatum (Linnaeus). Photograph by Samantha Gallagher. University of Florida.

Synonymy (Back to Top)

Apis manicata Linnaeus, 1758;
Apis pervigil Harris, 1776;
Apis maculata Fabricius,1781;
Apis fulvipes_homonym de Villers, 1789;
Apis modesta Christ, 1791;
Apis amoenita Christ, 1791;
Apis uncata Schrank, 1802;
Anthidium maculatum Latreille, 1806;
Anthidium marginatum Latreille, 1809;
Anthidium obtusatum Lepeletier, 1841;
Anthidium barbarum 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_homonym Gribodo, 1924;
Anthidium manicatum subcrenulata Alfken, 1931;
Anthidium (Anthidium) manicatum cyrenaica_homonym van der Zanden, 1992;
Anthidium (Anthidium) manicatum gribodoi Schwarz and Gusenleitner, 2003, replacement name;
Anthidium (Anthidium) manicatum gribodoi Schwarz and Gusenleitner, 2003, valid subspecies;
Anthidium (Anthidium) manicatum barbarum Lepeletier, 1841, valid subspecies” (Discover Life 2019.

Distribution (Back to Top)

Anthidium manicatum is native to Europe, western Asia, and northern Africa, but has expanded its range around the globe. It was accidentally introduced into the US and first recorded near Ithaca, New York, in 1963 (Pechuman 1967), and eventually expanded its range to Nova Scotia and parts of Utah (Gibbs and Sheffield 2009). It is likely the bee has been transported via nests in wood cavities and hollow plant stems (Strange et al. 2011). Current records indicate that the bee can be found in most of South America, especially along the east coasts of Brazil and Uruguay, across Asia and into Siberia and throughout New Zealand, and across most of the US and into southern Canada (Gibbs and Sheffield 2009). As of this publication, no records of the bee have been reported in Florida (Discover Life 2019), but given its broad distribution, its eventual presence in Florida would not be surprising.

Global distribution of Anthidium manicatum (Linnaeus).

Figure 2. Global distribution of Anthidium manicatum (Linnaeus). Map by Discover Life,, September 8, 2019.

Description (Back to Top)

Wool carder bees are somewhat large bees, 11 to 17 mm (7/16 to 5/8 inch) approximately the size of a honey bee. At a glance, wool carder bees could be mistaken for yellow jackets (Figure 1) since both display aposematic, bright yellow markings, but wool carder bees are hairier and more robust in shape than yellow jackets.

Male Anthidium manicatum (Figure 3) range from 14 to 17 mm (1/2 to 5/8 inch) and usually have more yellow on their bodies than do females, although color patterns can vary greatly. Males have light colored setae (hair-like structures) on their body and face and long setae on their legs. They have five sharp spines on the last segments of their abdomen. The spines are used while defending their territory from other bees (Gonzales and Griswold 2012).

Male Anthidium manicatum (Linnaeus).

Figure 3. Male Anthidium manicatum (Linnaeus). Illustration by Samantha Gallagher. University of Florida.

Female Anthidium manicatum(Figure 4) are smaller than males and are 11 to 13 mm (7/16 to 1/2 inch) in length. This is very unusual among bees as females are typically the larger sex. Females have large mandibles with sharp teeth used for collecting and manipulating plant trichomes (hairs) for their brood nests. They have short, dense, compact setae on their lower legs (the basitarsi) which help to organize the collected plant fibers into a ball. On the underside of their abdomens, they have white-to-amber colored hairs (scopa) used for collecting pollen (Gonzales and Griswold 2012).

Female Anthidium manicatum (Linnaeus).

Figure 4. Female Anthidium manicatum (Linnaeus). Illustration by Samantha Gallagher, University of Florida.

Life Cycle and Biology (Back to Top)

Anthidium manicatumare holometabolous insects and undergo complete metamorphosis. Wool carder bees are solitary bees. Each individual solitary female will find a nest site, lay eggs, collect food for the young, and construct all parts of the nest. Females use existing cavities for brood cell construction. Potential nest sites include cavities in wood such as those excavated by beetles or other insects, hollow plant stems and reeds, crevices and cracks in walls, and man-made bee houses (Figure 5) (Payne et al. 2011).

Rendition of life stages (in order from left to right: pupa, larva, egg, and adult female)

Figure 5. Rendition of life stages (in order from left to right: pupa, larva, egg, and adult female) inside of a cavity nest of Anthidium manicatum (Linnaeus). Note the pollen collecting hairs on the underside of the adult bee’s abdomen. Illustration by Samantha Gallagher, University of Florida.

The female uses her toothed mandibles to scrape trichomes off fuzzy plants and collects a ball of the material under her abdomen (Figure 6). She transports these soft plant fibers to her selected nest site and uses them to line a brood cell. Next, she collects and deposits a provision of pollen and nectar into the cell, enough pollen to feed a larva until it is ready to pupate. Lastly, she lays a single egg on top of the pollen and nectar supply before sealing the cell. The terminal plug is made from nearby particulate material including gravel, mulch, and bits of dried leaves (Payne et al. 2011).She will repeat this process with adjoining cells until the cavity is full (Payne et al. 2011).

Female Anthidium manicatum (Linnaeus) gathering fibers from rose campion

Figure 6. Female Anthidium manicatum (Linnaeus) gathering fibers from rose campion (Silene coronaria). Illustration by Samantha Gallagher. University of Florida.

A larva emerges from its egg and consumes the pollen provision while remaining in the nest cell. The larva grows, develops, pupates within the cell, and emerges from the nest as an adult. In most areas there are at least two generations a year (Severinghaus et al. 1981). Eggs laid in the fall will overwinter as prepupae and emerge as adults the following spring or early summer (Payne et al. 2011).

Male wool carder bees are notorious for their aggressive behavior defending floral resources for the females. A male will perch or hover near the preferred flowers of the female bees and act as a guard when other bees (including other male wool carders) invade his territory, quickly advancing on and thwarting any offending intruders. The purpose of this intense flower guarding is to provide females with sole access to resources in the male’s territory so that he can attempt to mate with the females (Pechuman 1967).

Hosts (Back to Top)

Anthidium manicatum females use trichomes derived mostly from European and Asian plants for their nests (Gibbs and Sheffield 2009). The most common plants utilized by female Anthidium manicatum for nesting material having abundant trichomes, like lamb’s ears (Stachys byzantina) and other plants in the mint (Lamiaceae) family (Hicks 2011). Other plants from which these bees harvest nesting material include rose campion (Silene coronaria) (Figure 6) and mulleins (Verbascum sp.). The plants are not thought to be damaged by this fiber harvesting.

Anthidium manicatum are generalist feeders, taking nectar from a variety of different plants (Figure 7). The most reported flowers visited by the bees for foraging are dead nettles, Stachys spp., various other mints (Lamiaceae family), peas and legumes (Fabaceae family), and figworts (Scrophulariaceae family) (Hicks 2011).

Female Anthidium manicatum (Linnaeus) visits oregano (Origanum vulgare)

Figure 7. Female Anthidium manicatum (Linnaeus) visits oregano (Origanum vulgare). Photograph by Samantha Gallagher, University of Florida.

Economic Importance (Back to Top)

Anthidium manicatum have proven to be very adaptable to a wide range of climates and habitats. Globally, the introduction and spread of non-native species exacerbates a loss in native species and threatens biodiversity (Gibbs and Sheffield 2009). Currently, Anthidium manicatum seem most populous in urban environments, which tend to offer more introduced plants than do natural areas (Gibbs and Sheffield 2009). Non-native bees often prefer non-native flowers, and when these are pollinated, there may be increased risk of the non-native plants spreading into and disrupting delicate ecosystems. As with any non-native bee species, there is concern of introducing pathogens that could infect native bees (Gibbs and Sheffield 2009).

The expanding range of Anthidium manicatum raises concerns of competition with native bees for critical resources such as nesting sites, pollen, and nectar (Gibbs and Sheffield 2009). Male Anthidium manicatum can be quite aggressive to other bees when defending floral territory, there has been some concern that they are killing honey (and other) bees (Pechuman 1967). Comba et al. (1999) observed declines in bumble bee visits to certain flowers when Anthidium manicatum males were present, so the impact of Anthidium manicatum in areas with sensitive bumble bee populations is something that should be surveyed and monitored (Gibbs and Sheffield 2009).

Selected References (Back to Top)