
Cuckoo Bees
In Minnesota, 23% of bee species are cuckoo bees. Cuckoo bees, also called cleptoparasitc bees or brood parasites, do not build their own nest. Instead, they lay their eggs in the nest of another bee (host), and their larvae consume the pollen provisions provided by the host. The host egg or larva must be destroyed after an egg is laid by the cuckoo bee. Many cuckoo bees leave this task to their larvae. In one of their instar stages, usually the non-feeding first instar stage, the larvae develop large mandibles that they employ to destroy the host egg or larvae. There are also social parasites: Cuckoo bumble bee (Bombus) females take over an active social Bombus nest and eliminate the host queen. In addition, sweat bees in the genus Lasioglossum invade and occupy social nests of bees in the same genus. In Minnesota, there are 11 genera and 120 cuckoo bee species that occur within three (of six) families.
Cuckoo bees that are brood parasites of solitary bees are wasp-like in appearance, have pitted exoskeletons and other anatomical features that help protect them if they are attacked by the host bee. They lack pollen-collecting structures and other nest-building anatomy such as soil moving and tamping structures present in ground-nesting bees or anatomical features that cavity-nesting bees use to collect supplemental nesting materials. One theory proposed to explain why some cuckoo bee females evade detection by their host is that they have a similar "smell" or chemical signature as the host.
Explore Cuckoo Bee Genera

The six species of Bombus in the subgenus Psithyrus are social parasites. Females in this subgenus take over an active Bombus nest and kill, drive out, or coexist with the host queen. The Psithyrus female then uses aggression and pheromones to coerce the queen's workers to help her rear her offspring. Unlike a typical Bombus nest with three castes (queen, workers, males), these social parasites have just two castes: females and males. Psithyrus females lack corbiculae (pollen baskets) and the abdominal glands to produce wax. They have a harder exoskeleton, longer sting, and larger ovaries than nest-establishing Bombus species. Some of these social parasites are very rare because their hosts are rare and/or threatened with extinction. In Minnesota, the most commonly observed cuckoo bumble bee is Bombus citrinus; its hosts include species that have relatively stable or increasing populations.

In Minnesota, there is only one species in the genus Brachymelecta —Brachymelecta interrupta. This cuckoo bee has one host, Anthophora walshii, a ground-nesting digger bee. Very little is known about the natural history or life cycle of this cuckoo bee. However, Anthophora walshii is known to nest in well-drained soils in grasslands.

All twelve Coelioxys species that occur in Minnesota are cleptoparasites of bees in the genus Megachile. Also called sharp-tailed cuckoo bees, Coelioxys females use their pointed abdomen to hide their egg in the layers of leaf pieces that line Megachile brood cells. The third instar Coelioxys larvae develop large sickle-like mandibles that they use to destroy the host egg or larvae. These large mandibles are not present in the following instar stages. Coelioxys females perch on vegetation or on an object such as a rock where they have a vantage point to watch and monitor the host's nest. When the host leaves, the Coelioxys female enters the nest and lays an egg in the leaf pieces in a partially provisioned brood cell.

Epeolus or cellophane cuckoo bees are cleptoparasites of ground-nesting bees in the genus Colletes. Epeolus females enter the host's nest, find a fully provisioned brood cell, then use spines on their sternum (underside of the abdomen) to create a hole in the cellophane-like brood cell lining. Through this hole they lay an egg, then secrete a fluid that attaches the egg to the interior of the lining and seals the hole in the lining. The first instar larva develops large mandibles used to destroy the host egg (suspended from the roof of the lining). It also develops lateral tubercles to help it stay afloat while feeding on the liquid provisions. By the second instar stage, the larva loses the large mandibles and lateral tubercles.

Just one species in the genus Holcopasites occurs in Minnesota—Holcopasites calliopsidis. This cuckoo bee is a specialist and has one host, Calliopsis andreniformis, a solitary ground-nesting bee. Holcopasites females monitor the host nest by perching on the ground or on vegetation near the nest. They enter an unoccupied nest, find a partially provisioned brood cell, then lay an egg on an angle into the cell wall under a piece of the cell lining. The first instar Holcopasites larva has oversized mandibles that it uses to kill the host egg and any other eggs in the brood cell. This cuckoo bee occurs in habitats that support its host, sites with patchy or bare well-drained soil and plants in the family Fabaceae growing nearby.

Non-parasitic Lasioglossum (Dialictus)
Of the eighty-four bee species in the genus Lasioglossum in Minnesota, four are social parasites of other species in the same genus. These parasitic females typically have large heads and mandibles, and no pollen-collecting structures. Unlike many other genera of cuckoo bees, they lack extensive pitting on their exoskeleton. Parasitic Lasioglossum have to get past the host Lasioglossum nest guards that either block or aggressively defend the nest entrance. Although the parasitic Lasioglossum have large mandibles that could be used to gain passage via aggression, Wcislo (1997) concluded that they instead likely use chemical signatures to deceive the nest guards.

Only one species in the genus Neolarra occurs in Minnesota — Neolarra vigilans. This rare cuckoo bee hosts include bees in the genus Perdita. All Perdita species in Minnesota are pollen specialists and typically nest in sandy or well-drained sites that include populations of their pollen host plants.

Bees in the genus Nomada are cleptoparasites of ground-nesting bees. In Minnesota, most of the hosts belong to the genus Andrena. With similar phenology to Andrena, most Nomada species are spring-active with the remaining minority active in summer and early autumn. Nomada females perch on sticks, leaf litter, rocks, or other objects on the ground near their hosts' nests. They can often be observed perching on the ground while actively fanning their wings next to a host nest entrance. It is not known how Nomada are not detected by the host, but one theory is that Nomada emit chemical signatures or pheromones that mimic the host.

Sphecodes, also called blood bees for their red abdomens, are cleptoparasites of several genera of ground-nesting bees. Twenty-six species of Sphecodes occur in Minnesota. Like other cuckoo bees, females can be found perching on the ground or on objects near the ground next to a host's nest. When the Sphecodes female enters an unoccupied nest, she lays an egg in a fully provisioned brood cell. The adult female also destroys the host egg, an atypical behavior as most cuckoo bee larva eliminate the host egg or larva.

Stelis are small black cuckoo bees that parasitize the cavity nests of bees in the genera Hoplitis, Heriades, and Osmia, all within the family Megachilidae. Stelis females enter a cavity nest and lay an egg in an open brood cell that is partially or fully provisioned with pollen. They conceal the egg in the provisions between the provisions and the wall of the brood cell, or they may lay the egg on the provisions. The Stelis larva, in one of its instar stages, kills the host larva.

Triepeolus are cleptoparasites of ground-nesting bees within the genera Epimelissodes, Melissodes, Dieunomia, and Xenoglossa. These cuckoo bees are active in summer and early autumn when both males and females visit flowers. Bees in this genus closely resemble cuckoo bees in the genus Epeolus, and the two can be very difficult to tell apart. In general, Epeolus are smaller than Triepeolus. Triepeolus females enter an unoccupied ground nest of the host and lay an egg attached to the cell wall in an open brood cell. The first instar Triepeolus larvae develop large sickle-like mandibles that are used to kill the host egg or larva. The second instar larvae lack these oversized mandibles.
Cuckoo Bee Species in Minnesota
Family | Scientific Name | Host | Host Nest |
---|---|---|---|
Apidae | Bombus ashtoni (B. bohemicus) | Bombus terricola, B. affinis. (Williams et al. 2014) | colony |
Apidae | Bombus citrinus | Bombus bimaculatus, B. impatiens, B. vagans (Gibbs 2023) | colony |
Apidae | Bombus flavidus (B. fernalde) | Recorded present in B. rufocinctus, B. occidentalis, and B. appositus nests. (Williams et al. 2014) | colony |
Apidae | Bombus insularis | Confirmed hosts: Bombus appositus, B. fervidus, B. flavifrons, B. nevadensis, B. ternarius. Present in nests of B. rufocinctus, B. nevadensis, B. occidentalis, B. terricola. (Williams et al. 2014) | colony |
Apidae | Bombus suckleyi | Bombus occidentalis confirmed host. Recorded present in B. terricola, B. rufocinctus, B. fervidus, B. nevadensis, and B. appositus nests. (Williams et al. 2014) | colony |
Apidae | Bombus variabilis | Bombus pensylvanicus (Williams et al. 2014) | |
Apidae | Brachymelecta interrupta | Anthophora walshii (Gibbs 2023) | ground |
Megachilidae | Coelioxys alternatus | Megachile pugnata (Gibbs 2023) | cavities |
Megachilidae | Coelioxys banksi | Megachile | |
Megachilidae | Coelioxys bisoncornuus | ||
Megachilidae | Coelioxys funerarius | Megachile (Gibbs 2023) | ground |
Megachilidae | Coelioxys immaculatus | Megachile | |
Megachilidae | Coelioxys modestus | Megachile campanulae (Gibbs 2023) | cavities |
Megachilidae | Coelioxys moestus | Megachile (Gibbs 2023) Megachile relativa (MN Bee Atlas) | cavities |
Megachilidae | Coelioxys octodentatus | Megachile (Gibbs 2023) Megachile rotundata (MN Bee Atlas) | ground |
Megachilidae | Coelioxys porterae | Megachile (Gibbs 2023) | cavities |
Megachilidae | Coelioxys rufitarsis | Megachile (Gibbs 2023) | ground |
Megachilidae | Coelioxys sayi | Megachile | |
Megachilidae | Coelioxys sodalis | Megachile (Gibbs 2023) | ground |
Apidae | Epeolus ainsliei | likely Colletes americanus and/or susannae (Wolf and Ascher 2009) and possibly C. wilmattae (Gibbs 2023) | ground |
Apidae | Epeolus americanus | Colletes consors mesocopus (Gibbs 2023) | ground |
Apidae | Epeolus autumnalis | Colletes compactus (presumed) (Ascher et al. 2014) | ground |
Apidae | Epeolus bifasciatus | Colletes latitarsis (presumed) (Mitchell 1962) | ground |
Apidae | Epeolus interruptus | Colletes aestivalis, C. brevicornis, & C. willistoni are possible hosts (Gibbs 2023). Present by/monitoring C. andrewsi nests. | ground |
Apidae | Epeolus lectoides | Colletes latitarsis (presumed) | |
Apidae | Epeolus lectus | Colletes | |
Apidae | Epeolus minimus | Colletes kincaidii is a likely host (Gibbs 2023) | ground |
Apidae | Epeolus pusillus | Colletes compactus and C. americanus | |
Apidae | Epeolus scutellaris | likely Colletes simulans armatus (Gibbs 2023) | ground |
Apidae | Holcopasites calliopsidis | Calliopsis andreniformis (Gibbs 2023) | ground |
Halictidae | Lasioglossum izawsum | Lasioglossum (Dialictus) (Gibbs 2011) | |
Halictidae | Lasioglossum michiganense | Lasioglossum (Dialictus) (Gibbs 2023) | ground |
Halictidae | Lasioglossum platyparius | Lasioglossum (Dialictus) (Gibbs 2011) | |
Halictidae | Lasioglossum rozeni | Lasioglossum (Dialictus) (Gibbs 2011) | |
Apidae | Neolarra vigilans | Perdita, likely P. perpallida (Portman 2023) | ground |
Apidae | Nomada aquilarum | Andrena (cnemidandrena)? (Gibbs 2023) | ground |
Apidae | Nomada articulata | Agapostemon (Gibbs 2023) | ground |
Apidae | Nomada australis | Agapostemon splendens? (Gibbs 2023) | ground |
Apidae | Nomada banksi | Andrena asteris (Espinoza et al. 2023) | ground |
Apidae | Nomada bella | ||
Apidae | Nomada besseyi | ||
Apidae | Nomada bethunei | ||
Apidae | Nomada cressonii | Andrena (Melandrena, Plastandrena) (Gibbs 2023) | ground |
Apidae | Nomada cuneata | Andrena vicina (Gibbs 2023) | ground |
Apidae | Nomada denticulata | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada depressa | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada erigeronis | ||
Apidae | Nomada fervida | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada fuscicincta | ||
Apidae | Nomada gracilis | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada graenicheri | ||
Apidae | Nomada illinoensis | ||
Apidae | Nomada imbricata | Andrena (melaandrena) (Gibbs 2023) | ground |
Apidae | Nomada integerrima | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada lehighensis | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada lepida | ||
Apidae | Nomada louisianae | ||
Apidae | Nomada luteoloides | Andrena (Melandrena) (Gibbs 2023) | ground |
Apidae | Nomada maculata | Andrena (Melandrena) (Gibbs 2023) | ground |
Apidae | Nomada obliterata | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada ovata | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada perplexa | ||
Apidae | Nomada pygmaea | ||
Apidae | Nomada rubi | ||
Apidae | Nomada rubicunda | Agapostemon splendens (Gibbs 2023) | ground |
Apidae | Nomada sayi | ||
Apidae | Nomada superba | ||
Apidae | Nomada tiftonensis | ||
Apidae | Nomada vegana | ||
Apidae | Nomada vicina | Andrena? (Gibbs 2023) | ground |
Apidae | Nomada vincta | Andrena helianthi (Gibbs 2023) | ground |
Apidae | Nomada xanthura | ||
Halictidae | Sphecodes antennariae | ||
Halictidae | Sphecodes atlantis | ground | |
Halictidae | Sphecodes banksii | Lasioglossum vierecki (Gibbs 2023) | ground |
Halictidae | Sphecodes clematidis | ground | |
Halictidae | Sphecodes confertus | ground | |
Halictidae | Sphecodes coronus | ground | |
Halictidae | Sphecodes cressonii | ground | |
Halictidae | Sphecodes davisii | ground | |
Halictidae | Sphecodes dichrous | ground | |
Halictidae | Sphecodes fattigi | ||
Halictidae | Sphecodes galerus | ||
Halictidae | Sphecodes heraclei | ||
Halictidae | Sphecodes hydrangeae | ||
Halictidae | Sphecodes illinoensis | ground | |
Halictidae | Sphecodes johnsonii | ground | |
Halictidae | Sphecodes levis | ground | |
Halictidae | Sphecodes mandibularis | ground | |
Halictidae | Sphecodes minor | ||
Halictidae | Sphecodes nigricorpus | ||
Halictidae | Sphecodes pecosensis | ground | |
Halictidae | Sphecodes pimpinellae | ||
Halictidae | Sphecodes prosphorus | ground | |
Halictidae | Sphecodes ranunculi | ||
Halictidae | Sphecodes smilacinae | ground | |
Halictidae | Sphecodes solonis | ground | |
Halictidae | Sphecodes townesi | ground | |
Megachilidae | Stelis coarctatus | Heriades, Hoplitis (Gibbs 2023) Heriades carinata (MN Bee Atlas) | cavities |
Megachilidae | Stelis foederalis | Hoplitis, Osmia (Gibbs 2023) | cavities |
Megachilidae | Stelis labiata | Hoplitis (Gibbs 2023), Hoplitis spoliata (Medler (1967) | cavities |
Megachilidae | Stelis lateralis | Hoplitis (Gibbs 2023), Hoplitis pilosifrons (Michener 1955), Hoplitis spoliata (Medler (1967) | cavities |
Megachilidae | Stelis nitida | cavities | |
Megachilidae | Stelis permaculata | Heriades carinata (Gibbs 2023, MN Bee Atlas) | cavities |
Megachilidae | Stelis subemarginata | Hoplitis, Osmia (Gibbs 2023) | cavities |
Apidae | Triepeolus concavus | Epimelissodes obliqua (Rightmyer 2008) | ground |
Apidae | Triepeolus cressonii | ||
Apidae | Triepeolus distinctus | Dieunomia (Rightmyer 2008) | ground |
Apidae | Triepeolus donatus | ||
Apidae | Triepeolus eliseae | possibly Melissodes (Eumelissodes) (Gibbs 2023) | ground |
Apidae | Triepeolus helianthi | possibly Melissodes (Eumelissodes) (Gibbs 2023) | ground |
Apidae | Triepeolus lunatus | Melissodes (Rightmyer 2008) | ground |
Apidae | Triepeolus obliteratus | possibly Melissodes (Eumelissodes) (Gibbs 2023) | ground |
Apidae | Triepeolus occidentalis | Melissodes, possibly M. menuachus (Gibbs 2023) | ground |
Apidae | Triepeolus pectoralis | Melissodes druriellus (Gibbs 2023) | ground |
Apidae | Triepeolus remigatus | Eucera (Peponapis) pruinosa and Dieunomia heteropoda
(Rightmyer 2008) | ground |
Apidae | Triepeolus rhododontus | ||
Apidae | Triepeolus simplex | ||
Apidae | Triepeolus subalpinus | Melissodes (Eumelissodes), possibly M. agilis (Gibbs 2023) | ground |
Apidae | Triepeolus tanneri |
Host Information: Minnesota Department of Natural Resources, Minnesota Bee Species List (August 2023).
https://files.dnr.state.mn.us/eco/mcbs/mn-statewide-bee-list.pdf
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Citations and Further Reading
Gibbs, J., Hanuschuk, E., Miller, R., Dubois, M., Martini, M., Robinson, S., ... & Onuferko, T. M. (2023). A checklist of the bees (Hymenoptera: Apoidea) of Manitoba, Canada. The Canadian Entomologist, 155, e3.
Hurd Jr, P. D., & Linsley, E. G. (1972). Parasitic bees of the genus Holcopasites Ashmead (Hymenoptera: Apoidea).
Mitchell, T. B. (1960). Bees of the eastern United States. Technical Bulletin No. 141. North Carolina Agricultural Experiment Station.
Odanaka, K. A. (2024). The Evolutionary History Of The Cleptoparasitic Bee Genus Nomada With An Emphasis On The Species Of Eastern North America. PhD Dissertation.
Portman, Z. M., Gardner, J., Lane, I. G., Gerjets, N., Petersen, J. D., Ascher, J. S., ... & Cariveau, D. P. (2023). A checklist of the bees (Hymenoptera: Apoidea) of Minnesota. Zootaxa, 5304(1), 1-95.
Rozen Jr, J. G. (1965). Biological notes on the cuckoo bee genera Holcopasites and Neolarra (Hymenoptera: Apoidea). Journal of the New York Entomological Society, 87-91.
Williams, P. H., Thorp, R. W., Richardson, L. L., & Colla, S. R. (2014). Bumble bees of North America: an identification guide. Princeton University Press.
Wcislo, W. T. (1997). Invasion of nests of Lasioglossum imitatum by a social parasite, Paralictus asteris (Hymenoptera: Halictidae). Ethology, 103(1), 1-11.
Page Photography Credits
Heather Holm
Joel Gardner CC BY-ND-NC 1.0 (Melittidae)
Steve Mlodinow CC BY-NC 4.0 (Brachymelecta)