Lasioglossum aeneiventre

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Lasioglossum aeneiventre
Scientific classification
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L. aeneiventre
Binomial name
Lasioglossum aeneiventre
Friese, 1916

Lasioglossum aeneiventre, also known as Dialictus aeneiventre, is a social sweat bee [1] and is part of the family Halictidae of the order Hymenoptera. [2] Found in Central America, it nests mostly on flat ground though sometimes in vertical banks. [3] It is often compared to L. figueresi . [4]

Contents

Taxonomy and phylogeny

L. aeneiventre is part of the subfamily Halictinae, of the hymenopteran family Halictidae. [2] The largest, most diverse and recently diverged of the four halictid subfamilies, [5] Halictinae (sweat bees) is made up of five tribes of which L. aeneiventre is part of Halictini, made up of over 2000 species. [6] Genus Lasioglossum is informally divided into two series: the Lasioglossum series and the Hemihalictus, [7] the latter of which L. aeneiventre is a part. [8] L. aeneiventre is part of the subgenus Dialictus which is made up mostly of New World species. [1]

Description and identification

L. aeneiventre is closely related morphologically to L. figueresi. In relation to L. figueresi, it is smaller and can be distinguished by wing color, patterns, punctate, and sternal and genital characteristics. In general, L. aeneiventre differs from other bees by its wings, pubescence, and markings. [4] There are also size differences between those of solitary female nests and those of multi-female nests, with solitary females being bigger than those of multi-female nests. [3]

Females

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Front of insect head diagram
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Hymenoptera morphology

A female L. aeneiventre can become a foundress and the queen, a worker, an auxiliary queen, or a replacement queen. In new nests, foundresses have unworn wings and mandibles, while in older multi-female nests, one female normally has worn wings while the other females do not. A female with worn wings has most likely survived from the previous generation. There is also seasonal size variation with emerging female offspring as big as solitary females in late April and May compared to being smaller earlier in the year. [3]

A female L. aeneiventre is recognized by its unique striped pattern on the front part of its mesothorax, the pattern of punctures on its front scutum of its middle thoracic segment, its larger size, its hair, and its slightly yellow wings including the membrane, veins, and stigma. Generally larger than males, it has a metallic dark-green head and a clypeal length greater than that of its supraclypeal area, which is slightly rounded and bulges. It does not have a frontal line ridge from below the base of the antenna to about half the distance between its antennal sockets to its median ocellus, and its lateral ocelli are slightly nearer to each other than to their compound eyes. It has punctures near its eyes, on the lower half of the clypeus, sometimes on the supraclypeal area, on the front part of its mesothorax and on the frons, while its gena and the interspaces of its supraclypeal area are shiny and its frons has dull spaces in between. In the middle of its thorax, it has a groove that is two-thirds the length of its metallic dark-green scutum of its middle thoracic segment, with deep punctures that divide as one moves towards the head, as well as about twelve stripes on each side which almost wrap around the propodeum. Its black metasoma is shiny and mostly smooth, its brown-tinted black legs are shiny and flattened on the front surface with a well-defined rim raised above the surface of the plate at the base of the tarsus, and its sharply rounded wings have dull yellow membranes with smokey tips. Its veins and stigma are brown. It has yellowish hair on its head, abundant white hair on its mesosoma, long, plumose, and golden hair on its metanotum, metasomal terga, and metasoma, white, short, and fine hair on its tegula, white fringed hair on the pseudopygidial area, and a dense golden band of hair on its pronotal lobe. [4]

Males

A male L. figueresi is distinct from other Dialictus by many of the female characteristics as well as those of its genitals. In comparison to a female, its compound eyes on its dark-green head converge more below and become wavy, and it has punctures on the clypeal area, vertex, and frons. Its scutum of its middle thoracic segment is widely separated by dull ground in the front and middle regions and has a deeply grooved middle line and a parapsidal line like in the female, its clypeus is dark green-purple with dark brown antennae that are lighter underneath, it has a brownish black tegula, and its terga has very close punctures with a shiny terga I-IV. Compared to the females, the male's wings are clearer, its veins are nearly brown, and its yellow to golden-yellow hair is sparser. [4]

Distribution and habitat

L. aeneiventre is a tropical bee that nests in the ground of highly disturbed, highly populated, and highly cultivated areas of Costa Rica's Mesenta Central. The nests are made of material that is easily accessible from their location. This region's weather consists of a dry season from late November or December until April or May and a subsequent wet season with a small period of less rain. They are found in groups of nests that are normally in flat ground but are occasionally in vertical banks. [3]

Nest structure

The nests of L. aeneiventre are made up of Earthen material, usually found close together. Symmetrical piles of dirt often surround the entrances of nests in flat ground and older nests in vertical banks, though these mounds are easily washed away by the rains. On flat ground, entrances are perpendicular to the surrounding land and descend straight down with only slight deviation or extend 10 to 18 cm in vertical banks. Older nests might also contain branches off the main tunnel. Cells 9 to 11 mm long and 3 to 4 mm in diameter bud off from the main tunnel without lateral tunnels. Due to used cells being plugged or filled with soil if they contain feces, old cells are considered not to be reused. There are also differences between solitary female nests and multi-female nests. Solitary female nests, generally newly created, have shorter tunnels and less cells than multi-female nests. [3]

Colony cycle

Unlike L. figueresi , L. aeneiventre function year-round, having up to three broods a year. They are only inhibited in October and November due to heavy rains. At the beginning of the dry season (late November to early December), a few new nests are created probably by newly emerged bees, while the majority of recently used nests are utilized again. These nests can expand up to 66 cells and 14 females by the end of the dry season in May. Females emerge from their nests in September and mate with other males; afterward they become inactive, only provisioning their cells during favorable weather. Males are seen throughout the year, and on average, about half of females in a nest in a given year are mated. The first broods of a year come out in late February. It also takes about 35 days for a larva to become an adult. [3]

Development and reproduction

The majority of solitary female L. aeneiventre found between June and October are mated with oocytes beginning to develop and sperm in their spermathecae. [3] Development, however, starts with the larvae, feeding on pollen and nectar, in the nest. [1] As they grow, males and females live together. When they become adults at around 35 days, they leave the nest and mate with others. Large solitary females produce smaller female offspring. However, there is no relation between body size and ovarian development. [3]

Behavior and ecology

The behavior of L. aeneiventre varies among nests and seasons. [3] Nests can be of different sizes and can have solitary females to "primitively eusocial" females, [3] meaning that the queen nudges outside workers to draw them back into the nest for easier stimulus by the queen. [9] Sometimes outside female L. aeneiventre usurp existing queens from their nests and take over operations. It is unlikely that altitude has a strong effect on the social organization of L. aeneiventre. [3]

Social organization

Nests can be maintained by one or more female L. aeneiventre. In solitary female nests, normally created at the beginning of the dry season, offspring emerge in late January and February. Female offspring would either emerge, mate, and found new colonies, or stay in the nest and become workers, auxiliary queens, or replacement queens. In nests headed by more than one female, there are more cells, and there is significant positive correlation between active cells per female and the number of females in the nest, suggesting that having more females leads to more efficient building and provisioning of cells. [3]

Circadian activity

Female L. aeneiventre begin their day between 7:30 and 8 AM when the temperature is greater than 18 °C (64 °F). They sit partly out of the entrance to their nest, most likely warming up their muscles needed for flight, and then forage until 2:30 to 3 PM. This activity occurs on clear or partly cloudy days yet stops during rain and low hanging clouds. [3]

Interaction with other species

L. aeneiventre interacts with plants and parasites. Plants provide it with pollen and nectar as food for both themselves and their larvae, while parasites invade their nests and affect their survival. They are parasitized much less than L. figueresi; [3] however they are more likely to be parasitized than bees living above the ground due to nest site. [10]

Diet

The diet of L. aeneiventre from larvae to adults consists of loaves of pollen mixed with nectar. The loaves can be made from different pollen sources due to the cooperative nature of provisioning and indicates that the pollen does come from different flowering plants. [3]

Parasites

There are several potential parasites of L. aeneiventre. Fly larvae (Diptera) and nematodes are found in some cells, and Conopidae and Strepsiptera are found internally in adult females. Additionally, the parasitic fly Phalacrotophora was seen flying at nests sites and could therefore be another parasite. [3]

Related Research Articles

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<i>Nomada</i> Genus of bees

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<i>Lasioglossum malachurum</i> Species of bee

Lasioglossum malachurum, the sharp-collared furrow bee, is a small European halictid bee. This species is obligately eusocial, with queens and workers, though the differences between the castes are not nearly as extreme as in honey bees. Early taxonomists mistakenly assigned the worker females to a different species from the queens. They are small, shiny, mostly black bees with off-white hair bands at the bases of the abdominal segments. L. malachurum is one of the more extensively studied species in the genus Lasioglossum, also known as sweat bees. Researchers have discovered that the eusocial behavior in colonies of L. malachurum varies significantly dependent upon the region of Europe in which each colony is located.

<i>Osmia bicornis</i> Species of bee

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Halictinae Subfamily of bees

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<i>Lasioglossum zephyrus</i> Species of bee

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". It is considered a primitively eusocial bee, although it may be facultatively solitary. The species nests in burrows in the soil.

<i>Halictus ligatus</i> Species of bee

Halictus ligatus is a species of sweat bee from the family Halictidae, among the species that mine or burrow into the ground to create their nests. H. ligatus, like Lasioglossum zephyrus, is a primitively eusocial bee species, in which aggression is one of the most influential behaviors for establishing hierarchy within the colony, and H. ligatus exhibits both reproductive division of labor and overlapping generations.

<i>Megachile campanulae</i> Species of bee

Megachile campanulae, known as the bellflower resin bee, is a species of bee in the family Megachilidae. Described in 1903, these solitary bees are native to eastern North America. Studies in 2013 placed them among the first insect species to use synthetic materials for making nests. They are considered mason bees, which is a common descriptor of bees in several families, including Megachilidae. Within the genus Megachile, frequently also referred to as leafcutter bees, M. campanulae is a member of the subgenus Chelostomoides, which do not construct nests from cut leaves, but rather from plant resins and other materials. Females lay eggs in nests constructed with individual cell compartments for each egg. Once hatched, the eggs progress through larval stages and subsequently will overwinter as pupae. The bees are susceptible to parasitism from several other bee species, which act as brood parasites. They are medium-sized bees and the female adults are typically larger than the males. They are important pollinators of numerous native plant species throughout their range.

<i>Megalopta genalis</i> Species of bee

Megalopta genalis is a species of the family Halictidae, otherwise known as the sweat bees. The bee is native to Central and South America. Its eyes have anatomical adaptations that make them 27 times more sensitive to light than diurnal bees, giving it the ability to be nocturnal. However, its eyes are not completely different from other diurnal bees, but are still apposition compound eyes. The difference therefore lies purely in adaptations to become nocturnal, increasing the success of foraging and minimizing the danger of doing so from predation. This species has served as a model organism in studies of social behavior and night vision in bees.

<i>Lasioglossum cressonii</i> Species of insect

Lasioglossum cressonii is a species in the sweat bee genus Lasioglossum, family Halictidae. Halictidae exhibit eusocial hierarchy behavior which is interesting given that eusociality in this group is hard to evolve and easy to lose. L. cressonii is found throughout North America. L. cressonii have been shown to be important pollinators for apple trees and many other North American native plants. A common name is Cresson's metallic sweat bee.

<i>Lasioglossum vierecki</i> Species of bee

Lasioglossum vierecki, also known as Dialictus vierecki and Halictus vierecki, is a sand sweat bee and is part of the family Halictidae of the order Hymenoptera. It is found in the eastern half of North America from Minnesota to the New England States down to Georgia and Louisiana and up in Manitoba and Ontario. Commonly found in sandy areas, it pollinates various flowers such as grass-leaved goldenrod and rattlesnake master.

<i>Lasioglossum hemichalceum</i> Species of bee

Lasioglossum hemichalceum, which has sometimes been confused with L. erythrurum, is a sweat bee endemic to Australia. Large numbers of unrelated females will typically share a single nest, a behavior referred to as "communal". Nests are constructed underground by the independent efforts of the females. L. hemichalceum will typically begin creating new colonies during the summer, with brood production from late November through the first few months of spring. Members of this species do not demonstrate aggressive behavior towards one another. As the size of the colony increases, the reproductive potential of each female does not change, unlike many species of bees.

Lasioglossum figueresi, formerly known as Dialictus figueresi, is a solitary sweat bee that is part of the family Halictidae of the order Hymenoptera. Found in Central America, it nests in vertical earthen banks which are normally inhabited by one, though sometimes two or even three, females. Females die before their larvae hatch. It was named after José Figueres Ferrer, a famous Costa Rican patriot, and studies of its behavior are now general models for social behavior studies.

<i>Lasioglossum leucozonium</i> Species of bee

Lasioglossum leucozonium, also known as Lasioglossum similis, is a widespread solitary sweat bee found in North America, Europe, Asia, and parts of northern Africa. While now a common bee in North America, population genetic analysis has shown that it is actually an introduced species in this region. This population was most likely founded by a single female bee.

<i>Augochlora pura</i> Species of insect

Augochlora pura is a solitary sweat bee found primarily in the Eastern United States. It is known for its bright green color and its tendency to forage on a variety of plants. Inhabiting rotting logs, this bee can produce up to three generations per year. Both males and females have been observed licking sweat from human skin, most likely seeking salt

<i>Halictus sexcinctus</i> Species of bee

Halictus sexcinctus, commonly referred to as the six-banded furrow bee, is a species of sweat bee found throughout Europe and as far east as Asian Turkey and Iraq.The H. sexcinctus can be easily confused with the closely related species, Halictus scabiosae, due to very similar morphological features. H. sexcinctus show a social polymorphism in which different colonies can exhibit solitary, communal, or eusocial structure. Due to this large variance in social organization, it was suspected that it was not one species at all, but rather multiple, cryptic species. However, genetic analysis was able to confirm these varying populations as one species. H. sexcinctus will forage from multiple flower species, but prefers plant species with wide-open flowers. Their nests can be found dug into the ground in loamy or sandy soil.

Dialictus Subgenus of insects

Dialictus is a subgenus of sweat bees belonging to the genus Lasioglossum. Most of the members of this subgenus have a metallic appearance, while some are non-metallic. There are over 630 species worldwide. They are commonly found in the Northern Hemisphere and are found in abundance in North America. Members of this subgenus also have very diverse forms of social structure making them model organisms for studying the social behavior of bees.

<i>Augochlorella</i> Genus of bees

Augochlorella is a genus in the bee family Halictidae, commonly called sweat bees. They display metallic coloration, ranging from reddish to gold to bluish green, as is typical for other genera in the tribe Augochlorini.

<i>Megalopta</i> Genus of bees

Megalopta is a widespread neotropical genus in the tribe Augochlorini in family Halictidae, known as the sweat bees. They are the largest of the five nocturnal genera in Augochlorini. Most have pale integumentary pigmentation, and all have large ocelli, most likely a feature of their nocturnal behavior. They live in tropical central America and the entirety of South America. The subgenus Noctoraptor is cleptoparasitic. They are not known from the fossil record.

References

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  2. 1 2 "Lasioglossum aeneiventre". Integrated Taxonomic Information System . Retrieved 11 October 2015.
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  8. Danforth B. N. and Wcislo W. T. (1999). "Two New and Highly Apomorphic Species of the Lasioglossum Subgenus Evylaeus (Hymenoptera: Halictidae) from Central America" (PDF). Ann. Entomol. Soc. Am., 92(5), 630.
  9. Fletcher, D.; Ross K. (1985). "Regulation of Reproduction in Eusocial Hymenoptera". Annual Review of Entomology. 30: 319–343. doi:10.1146/annurev.ento.30.1.319.
  10. Wcislo W. T. (1996). "Parasitism rates in relation to nest site in bees and wasps (Hymenoptera: Apoidea)" (Abstract). Journal of Insect Behavior, 9(4), 643-656.