Andrena prunorum

Andrena prunorum, otherwise known as the purple miner bee, is a species of solitary bees in the family Andrenidae.[1] It is commonly found in the continental United States as well as much of North and Central America.[2][3] Andrena prunorum is a spring-flying, ground-nesting bee that serves as a ubiquitous generalist in ecological settings. Both males and females live as prepupae in the winter in which they mate, and the females seek new sites for ground burrows. From there, they construct small cells surrounding a ball of pollen combined with nectar to nourish a laid egg before each cell is sealed, and the cycle begins anew.[4] A. prunorum generally prefer the pollen derived from Rosaceae plants but will pollinate fruit trees if given the opportunity.[2]

Andrena prunorum
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Andrenidae
Genus: Andrena
Species:
A. prunorum
Binomial name
Andrena prunorum
Cockerell, 1896

Geography

Habitat

A. prunorum is commonly found in much of North and Central America. The Andrenidae family was found to be the second-most represented in British Columbia.[1] This is compounded by the finding that about 70% of the solitary bee species in eastern Canada nest in the ground.[1] However, these findings may be unreliable as Andrena is not readily identifiable, so the isolation of A. prunorum specifically has been a vexing challenge for researchers.[1] They tend to inhabit grasslands containing vernal pools.[5]

Biology

Life Cycle and Behavior

A. prunorum is a solitary bee species in which every female is fertile and inhabits a nest constructed by herself which differs from social bee species in the sense that there is no division of labor since there are no designated queen and worker bees for the species.[6]

Typically small in size, they often can be mistaken for a fly if not observed closely. Solitary bees like A. prunorum tend to emerge in the spring when their host flowers are blooming. After mating, the females dig nests that begin with tunnels going straight into the ground for a few inches. From there, a side tunnel is dug which ends in a brood chamber about 1 cm wide and 2 cm tall. After coating the chamber with a waxy substance, the female bee begins to collect pollen and nectar which are made into a ball about 6–8 mm across. A single egg gets deposited, and the chamber gets sealed up and another brood chamber gets constructed with a single female capable of digging 8-10 chambers. The egg hatches, and the larva proceeds to consume the pollen ball. In the autumn the larva molts into an adult and spends the winter resting in its chamber. It emerges the following spring, and the cycle repeats.[5]

Male Roles

Males, otherwise known as drones, are haploid and have shorter lifespans than females. Their primary purpose is to fertilize a receptive female, and they die immediately after mating. They have been observed patrolling cultivated fruit trees just before and after bloom.[7]

Female Roles

Females live much longer lifespans from three to five years and display more complex behavior in maintenance and mating patterns. To build nests, females display the ability to conceal burrows within vegetation while remaining a consistent distance apart from neighboring bees. In locating their nests, they can perform orientation flights in a rough figure-eight pattern.[7] Females produce neither honey nor beeswax but pollen and nectar are collected to feed their young.[6]

Subspecies

References

  1. Sheffield, Cory S.; Heron, Jennifer M. (2019-03-05). "The bees of British Columbia (Hymenoptera: Apoidea, Apiformes)". Journal of the Entomological Society of British Columbia. 115: 44–85. ISSN 1929-7890.
  2. Tepedino, Vincent J.; Alston, Diane Gail; Bradley, Brosi A.; Toler, Trent R.; Griswold, Terry L. (2007-10-01). "Orchard pollination in Capitol Reef National Park, Utah, USA. Honey bees or native bees?". Biodiversity and Conservation. 16 (11): 3083–3094. doi:10.1007/s10531-007-9164-8. ISSN 1572-9710. S2CID 2317408.
  3. Galbraith, Sara M.; Cane, James H.; Moldenke, Andrew R.; Rivers, James W. (2019). "Wild bee diversity increases with local fire severity in a fire-prone landscape". Ecosphere. 10 (4): e02668. doi:10.1002/ecs2.2668. ISSN 2150-8925.
  4. Wood, Thomas J.; Roberts, Stuart P.M. (2017-11-01). "An assessment of historical and contemporary diet breadth in polylectic Andrena bee species". Biological Conservation. 215: 72–80. doi:10.1016/j.biocon.2017.09.009. ISSN 0006-3207.
  5. "Solitary Bees". Sacramento Splash. Retrieved 2021-05-26.
  6. Grimaldi, David A; Engel, Michael S (2005). Evolution of the insects. Cambridge [U.K.]; New York: Cambridge University Press. ISBN 978-0-521-82149-0. OCLC 56057971.
  7. Miliczky, Eugene (2008). "Observations on the Nesting Biology of Andrena (Plastandrena) prunorum Cockerell in Washington State (Hymenoptera: Andrenidae)". Journal of the Kansas Entomological Society. 81 (2): 110–121. doi:10.2317/JKES-611.12.1. ISSN 0022-8567. JSTOR 25086427. S2CID 83703454.
  8. Laberge, Wallace E. (1969). "A Revision of the Bees of the Genus Andrena of the Western Hemisphere. Part II. Plastandrena, Aporandrena, Charitandrena". Transactions of the American Entomological Society. 95 (1): 1–47. ISSN 0002-8320. JSTOR 25077972.
  9. Miliczky, E. R.; Osgood, E. A. (1995). "Bionomics of Andrena (Melandrena) vicina Smith in Maine and Washington, with New Parasite Records for A. (M.) regularis Malloch and a Review of Melandrena Biology". Journal of the Kansas Entomological Society. 68 (1): 51–66. ISSN 0022-8567. JSTOR 25085560.
  10. Kuhlman, Marirose; Burrows, Skyler (2017-03-30). "Checklist of bees (Apoidea) from a private conservation property in west-central Montana". Biodiversity Data Journal. 5 (5): e11506. doi:10.3897/BDJ.5.e11506. ISSN 1314-2828. PMC 5515105. PMID 28765718.

Further reading

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.