Lasioglossum zephyrus

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Lasioglossum zephyrus
Sweat Bee (Lasioglossum zephyrum) and a Cuckoo Wasp (8084530876).jpg
L. zephyrus (bottom) with a cuckoo wasp
Scientific classification
Kingdom:
Animalia
Phylum:
Arthropoda
Class:
Insecta
Order:
Hymenoptera
Family:
Halictidae
Genus:
Lasioglossum
Species:
L. zephyrus
Binomial name
Lasioglossum zephyrus
(Smith, 1853)[1]
Synonyms
  • Halictus zephyrus Smith, 1853
  • Halictus (Chloralictus) academicus Sandhouse, 1924
  • Halictus (Chloralictus) vintonensis Sandhouse, 1924
  • Lasioglossum zephyrum Auctt. (Missp.)
  • Lassioglossum [sic] zypherum Falin, 2003 (Missp.)

Lasioglossum zephyrus is a sweat bee of the family Halictidae, found in the U.S. and Canada. It appears in the literature primarily under the misspelling "zephyrum".[1] It is considered a primitively eusocial bee (meaning that they do not have a permanent division of labor within colonies),[2] although it may be facultatively solitary (i.e., displaying both solitary and eusocial behaviors).[1][3] The species nests in burrows in the soil.

Taxonomy and phylogeny[]

The order Hymenoptera contains more eusocial species than any other order.[4] Eusociality has many origins and is present in many degrees within Hymenoptera, with L. zephyrus being one of the more primitive examples.[2][4] The genus Lasioglossum is predominantly eusocial, but has a high level of variation in sociality.[4] For instance, Lasioglossum zephyrus, as well as another species of this family of bees, Halictidae, Halictus ligatus, are known for their characteristic primitively eusocial behavior. This unique type of eusociality gives insight about the evolutionary background of eusociality of these species.[5] Six species within this genus have reverted to solitary life, social polymorphism, or parasitism.[4]

Description and identification[]

Lasioglossum zephyrus is characterized by its dark green metallic color, reddish abdomen, and a hairier face than most other species. Males are 6 to 7 millimeters long, slightly larger than females. Males are distinguished from females by their brighter green color and redder abdomens.[6] Since the castes vary along a spectrum, there is no definite way to distinguish a worker from a queen based on appearance alone.[7] However, queens can be identified by their behavior, pushing subordinates down in the nest and nudging them to inhibit their reproduction.[8]

Distribution and habitat[]

L. zephyrus has been found throughout the United States, in the months of March through October.[6][9] Nests are usually constructed in April along the south facing edges of streams, and are clustered in aggregations of up to 1,000 nests.[7][10] It nests in burrows that are typically constructed by young females. However, older females may also contribute to burrowing if their nests have been destroyed. These females excavate primarily at night, but activity has been reported throughout the day. Workers use their mandibles to loosen the soil, then carry it a short distance to be picked up by another bee. This soil is ultimately smoothed over the walls or used to fill evacuated old burrows. Females excavate cells and line them with a liquid produced in their enlarged Dufour's glands and secreted from the apex of the abdomen.[9]

Colony cycle[]

Lasioglossum zephyrus nests consist of less than 20 individuals.[9] During the spring, around April, new nests are established by one or more females.[7][9] Some of these nest may never gain more members, and the female will remain solitary. If they do expand, the colony will reach its maximum size of 10–20 around August.[3][9] Growth of the colony is gradual throughout the summer.[7] Inseminated young queens overwinter in their nests so that the cycle may be repeated.[3][7] However, overwintered queens are likely to die early on in the summer. After the death of an old queen, a new queen takes over within hours.[9] L. zephyrus colonies have a high mortality rate, especially when inhabited by a solitary bee lacking guards.[7][8]

Behavior[]

Dominance hierarchy[]

Roles within the colony are indirectly determined by age or physical differences, but direct determination is made by dominance interactions.[9] This type of hierarchy is very different from other species of bees, such as Lasioglossum hemichalceum, which is characterized by its egalitarian behavior and lack of aggression. All female L. hemichalceum are able to reproduce and cooperate to raise their young.[11] Queens have been shown to back workers into the depths of the burrows, preventing them from foraging and growing larger queen sized ovaries.[8] The tendency to display these behaviors is not influenced by the genetic relatedness of the subordinate bee, but it does decrease with time. In general, within colonies more closely related, there tends to be less aggression between bees.[12] When the queen dies, another worker takes her place and begins reproduction.[8] Among females, queens are at the top of the dominance hierarchy with their developed ovaries. Second are the guards, with some ovarian development. Foragers are the most subordinate group.[12]

Division of labor[]

Young females are responsible for constructing the nest. As adults, Lasioglossum zephyrus females become either mated egg-layers or workers who forage, guard, and make cells.[9] In a typical Lasioglossum zephyrus colony, the oldest females tend to be mated queens. However, among similarly aged bees, the largest is generally the queen.[3] The queen does not collect pollen or construct cells after her first batch of workers has hatched.[13] Queens and workers are not very physically distinct, since bee size varies on a continuum.[3]

Male behavior[]

Males are not considered productive members of the nest since they do not remain in their home nests. Instead, they form swarms around clusters of nests as early as 2 days after hatching.[7][14][15] Early in the spring, the males are solitary or clustered in small groups, but by late summer they gather in swarms of thousands of bees. Within these swarms there are head-on collisions between bees as they search for females and flowers.[15] While foraging, L. zephyrus searches for flowers, sometimes even forcing them open in order to get first access to the pollen.[16] Males have been seen landing on small pebbles and small objects as if they were females and have been observed mating as young as 4 days old up until death. In the laboratory, males were observed to have specific patrolling routes, flying between specific objects in sequence. They sleep in holes, plants, or abandoned burrows, solitarily or in small groups.[15]

Reproductive suppression[]

Most queens will mate during their lifetimes, but some workers may mate as well since they are physiologically capable.[3] In fact, about 18% of workers mate successfully between the months of June and August. When a queen is present, workers are not typically receptive to mating.[14] Females have been shown to partake in egg cannibalism, eating the eggs of nest mates, thus inhibiting their reproduction,[9] as well as the aggressive behaviors described in the dominance hierarchy subsection.

Mating behavior[]

Mating tends to take place near the nest's entrance, where the males typically fly.[14] Males will pursue females on land, but not in the air, and have been shown to aggressively attack females at the nest's entrance. Males will approach and occasionally grasp bees of other species, but no heterospecific matings have been documented. Females secrete an odor that functions as an aphrodisiac and a sex attractant. This odor is produced by female virgins between the ages of 2 and 8 days. The courtship period is short, and copulation occurs with the male above the female. In the field, L. zephyrus has been seen to copulate for 10–42 seconds. Most of the males' attempts at mating were met with resistance, but the females tend to remain relatively motionless during copulation. Many females are successful at preventing unwanted matings, suggesting that they have at least some control over their choice of mate. As many as four males have been observed stacked on top of a copulating male in attempt to mate with that female.[17]

Communication and recognition[]

Individual bees can recognize their nest and nest mates by their odors, which helps to prevent parasitism by unrelated L. zephyrus as well as other species.[18][19] This recognition has been documented in both males and females. Males can identify individual females by their unique odors and learn to avoid females who are unreceptive to mating.[19] L. zephyrus has also been shown to leave foreign nests even without being attacked, which supports the theory that they use odors to identify their home nests.[18]

Kin selection[]

Genetic relatedness[]

Haplodiploid sex determination

In Hymenoptera species, like Lasioglossum zephyrus, females are diploid and males are typically haploid, in a system called haplodiploidy. However, in inbred L. zephyrus populations, and also in other hymenopteran species, diploid males have been discovered.[20] Hymenopteran workers are expected to be related by a coefficient of 3/4, assuming the queen only mates only once.[10][14] However, in those nests studied, the relatedness coefficient was found to be lower, around 0.7. This could be explained by the insemination of multiple queens. With a relationship this high, significant altruism is likely.[10] The workers share only half of their genes with the queen, so they have more genes in common with their sisters. Since workers are more closely related to their sisters than their own offspring, whose relationship coefficient would be 0.5, kin selection has been proposed as an additional reason why workers mate so infrequently. They can pass down more genes through sisters than the same number of direct offspring.[14] Nests have been shown to be more genetically similar to nests in close proximity.[10]

Kin recognition and discrimination[]

Once an individual has learned the odor of its kin, it can successfully identify kin it has never met, since odors are genetically determined. Additionally, it can determine whether this relative is a close or distant relative.[21] While learning does play a role in kin recognition, the genetic differences in odor are thought to be more critical in kin recognition. Kin recognition is beneficial for defense of the entire nest, as well as at the individual level. Individuals benefit by contributing only to the fitness of their own related nest mates.[18]

Diet[]

Adult Lasioglossum zephyrus feed their larva pollen from surrounding plants. Since they forage at a variety of different flowers, they collect multiple types of pollen. Some types are more protein dense than others, but the adults do not compensate for the difference in pollen quality. All offspring receive the same amount of pollen, which results in offspring of different sizes. Size is an advantage for females because it gives them a better chance of becoming a queen. They also tend to produce more eggs of better quality, and greater size increases the chance that a female survives the winter. Larger males are better able to defend territories and compete for mates. Size is also a factor for both species in regards to flight. Larger body size leads to an increased body temperature and the ability to fly sooner in the season and with greater frequency.[22] This species has been observed forcing open unbloomed flowers of species Xyris tennesseensis to extract the pollen, ensuring first and exclusive access.[16]

Interactions[]

Parasites[]

L. zephyrus has been parasitized by diverse organisms including bacteria, fungi, protozoa, and other species of hymenoptera. Nematodes have been found in the abdominal cavities of L. zephyrus females, and have led to a reduction in ovarian development. Parasites that attack in the spring during nest founding tend to be most successful. If threatened, the bee may try to attack it or decapitate the intruder. Guard bees are often responsible for the protection of the nest and will send one member to attack while the others block the entrance with their abdomens.

Nematode removed from the abdominal cavity of a hornet

Nests containing only infected females are in danger of dying out. While infected bees are able to excavate burrows, they are less active than healthy bees and do not collect pollen to make cells.

Gregarine protozoa have been found generally in older specimens of L. zephyrus. It is thought that once a bee is infected, it takes time for the spores to fully develop. These parasites have only been found in females, although it is unclear why males remain unaffected.[7]

The bee species is a kleptoparasite of L. zephyrus.[7] The mutillid is also a parasitoid, and known to engage in aggressive fights with female L. zephyrus. Instead of stinging its opponent, L. zephyrus attempts to decapitate it. The mutillid retreats, unable to defend itself.[7]

References[]

  1. ^ a b c "Species Lasioglossum zephyrus". BugGuide. Retrieved 2019-06-24.
  2. ^ a b Batra, S. W. T. 1966. The life cycle and behavior of the primitively social bee Lasioglossum zephyrum (Halictidae). Univ. Kansas Sci. Bull. 46:359–423.
  3. ^ a b c d e f Interactions in colonies of primitively social bees: Artificial colonies of Lasioglossum zephyrum. PNAS. Retrieved 08-27-2011.
  4. ^ a b c d Danforth, Bryan N.; Conway, Lindsay; Ji, Shuqing (2003-02-01). "Phylogeny of Eusocial Lasioglossum Reveals Multiple Losses of Eusociality within a Primitively Eusocial Clade of Bees (Hymenoptera: Halictidae)". Systematic Biology. 52 (1): 23–36. doi:10.1080/10635150390132687. ISSN 1063-5157. PMID 12554437.
  5. ^ Pabalan, N.; Davey, K.G.; Packer, L. (2000). "Escalation of Aggressive Interactions During Staged Encounters in Halictus ligatus Say (Hymenoptera: Halictidae), with a Comparison of Circle Tube Behaviors with Other Halictine Species'". Journal of Insect Behavior. 13 (5): 627–650. doi:10.1023/A:1007868725551. S2CID 20773517.
  6. ^ a b "Discover Life". Retrieved September 19, 2015.http://www.discoverlife.org/20/q?search=Lasioglossum+zephyrum
  7. ^ a b c d e f g h i j Batra, Suzanne W. T. (1965-10-01). "Organisms Associated with Lasioglossum zephyrum (Hymenoptera: Halictidae)". Journal of the Kansas Entomological Society. 38 (4): 367–389. JSTOR 25083474.
  8. ^ a b c d Michener, Charles D.; Brothers, Denis J. (1974-03-01). "Were Workers of Eusocial Hymenoptera Initially Altruistic or Oppressed?". Proceedings of the National Academy of Sciences. 71 (3): 671–674. Bibcode:1974PNAS...71..671M. doi:10.1073/pnas.71.3.671. ISSN 0027-8424. PMC 388074. PMID 16592144.
  9. ^ a b c d e f g h i Batra, Suzanne W. T. (1964-06-01). "Behavior of the social bee, Lasioglossum zephyrum, within the nest (Hymenoptera: Halictidæ)". Insectes Sociaux. 11 (2): 159–185. doi:10.1007/BF02222935. ISSN 0020-1812. S2CID 37684424.
  10. ^ a b c d Crozier, R. H.; Smith, B. H.; Crozier, Y. C. (1987-07-01). "Relatedness and Population Structure of the Primitively Eusocial Bee Lasioglossum zephyrum (Hymenoptera: Halictidae) in Kansas". Evolution. 41 (4): 902–910. doi:10.2307/2408898. JSTOR 2408898. PMID 28564347.
  11. ^ Kukuk, Penelope F. (1992-01-12). "Social Interactions and Familiarity in a Communal Halictine Bee Lasioglossum (Chilalictus) hemichalceum". Ethology. 91 (4): 291–300. doi:10.1111/j.1439-0310.1992.tb00870.x. ISSN 1439-0310.
  12. ^ a b Smith, Brian H. (1987-02-01). "Effects of genealogical relationship and colony age on the dominance hierarchy in the primitively eusocial bee Lasioglossum zephyrum". Animal Behaviour. 35 (1): 211–217. doi:10.1016/S0003-3472(87)80226-9. S2CID 53191126.
  13. ^ Michener, Charles D.; Brothers, Denis J.; Kamm, Dwight R. (1971-04-01). "Interactions in Colonies of Primitively Social Bees: II, Some Queen-Worker Relations in Lasioglossum zephyrum". Journal of the Kansas Entomological Society. 44 (2): 276–279. JSTOR 25082413.
  14. ^ a b c d e Greenberg, Les; Buckle, Gregory R. (1981-12-01). "Inhibition of worker mating by queens in a sweat bee, Lasioglossum zephyrum". Insectes Sociaux. 28 (4): 347–352. doi:10.1007/BF02224192. ISSN 0020-1812. S2CID 32725534.
  15. ^ a b c Barrows, Edward M. (1976). "Mating Behavior in Halictine Bees (Hymenoptera: Halictidae): I, Patrolling and Age-Specific Behavior in Males". Journal of the Kansas Entomological Society. 49 (1): 105–119. JSTOR 25082792.
  16. ^ a b Wall, M. A.; Teem, A. P.; Boyd, R. S. (Mar 2002). "Floral Manipulation by Lassioglosssum zephyrum (Hymenoptera: Halictidae) Ensures First Access to Floral Rewards by Initiating Premature Anthesis of Xyris tennesseenis (Xyridaceae) Flowers". Florida Entomologist. 85 (1): 290–291. doi:10.1653/0015-4040(2002)085[0290:fmblzh]2.0.co;2.
  17. ^ Barrows, Edward M. (1975-09-01). "Mating behavior in halictine bees (Hymenoptera: Halictidae): III. Copulatory behavior and olfactory communication". Insectes Sociaux. 22 (3): 307–331. doi:10.1007/BF02223079. ISSN 0020-1812. S2CID 27101766.
  18. ^ a b c Kukuk, Penelope F.; Breed, Michael D.; Sobti, Anita; Bell, William J. (1977-01-01). "The Contributions of Kinship and Conditioning to Nest Recognition and Colony Member Recognition in a Primitively Eusocial Bee, Lasioglossum zephyrum (Hymenoptera: Halictidae)". Behavioral Ecology and Sociobiology. 2 (3): 319–327. doi:10.1007/bf00299743. JSTOR 4599139. S2CID 7582510.
  19. ^ a b Wcislo, William T. (1987-03-01). "The role of learning in the mating biology of a sweat bee Lasioglossum zephyrum (Hymenoptera: Halictidae)". Behavioral Ecology and Sociobiology. 20 (3): 179–185. doi:10.1007/BF00299731. ISSN 0340-5443. S2CID 8349439.
  20. ^ Kukuk, Penelope F.; May, Bernie (1990-09-01). "Diploid Males in a Primitively Eusocial Bee, Lasioglossum (Dialictus) zephyrum (Hymenoptera: Halictidae)". Evolution. 44 (6): 1522–1528. doi:10.2307/2409334. JSTOR 2409334. PMID 28564310.
  21. ^ Greenberg, Les (1988-07-01). "Kin recognition in the sweat bee, Lasioglossum zephyrum". Behavior Genetics. 18 (4): 425–438. doi:10.1007/BF01065512. ISSN 0001-8244. PMID 3190637. S2CID 44298800.
  22. ^ Roulston, T'ai H.; Cane, James H. (2002-01-01). "The effect of pollen protein concentration on body size in the sweat bee Lasioglossum zephyrum (Hymenoptera: Apiformes)". Evolutionary Ecology. 16 (1): 49–65. doi:10.1023/A:1016048526475. ISSN 0269-7653. S2CID 23594452.

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