Lasioglossum figueresi

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Lasioglossum figueresi
Scientific classification
Kingdom:
Animalia
Phylum:
Arthropoda
Subphylum:
Hexapoda
Class:
Insecta
Order:
Hymenoptera
Family:
Halictidae
Subfamily:
Halictinae
Tribe:
Halictini
Genus:
Lasioglossum
Species:
L. figueresi
Binomial name
Lasioglossum figueresi
Wcislo, 1990

Lasioglossum figueresi, formerly known as Dialictus figueresi, is a solitary sweat bee [1] that is part of the family Halictidae of the order Hymenoptera. [2] 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. [3] 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. [4]

Contents

Taxonomy and phylogeny

L. figueresi 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. figueresi is part of Halictini, which is made up of over 2000 species. [6] Genus Lasioglossum is informally divided into two series: the Lasioglossum series and the Hemihalictus. [7] L. figueresi belongs to the latter and is part of the subgenus Dialictus which is made up mostly of New World species. [1] [8] It is most closely related to L. marginatum, L. politum, [9] and L. aeneiventre . [10]

Description and identification

L. figueresi is closely related morphologically to L. aeneiventre . Unusually large, it is described in relation to L. aeneiventre as well as other Dialictus. In general, L. figueresi differs from other bees by its wings, hair, and markings. [10]

Females

Front of insect head diagram Front of insect head diagram.svg
Front of insect head diagram
Hymenoptera morphology HoneyBeeAnatomy.png
Hymenoptera morphology

A female L. figueresi is recognized from L. aeneiventre and other Dialictus by its unique striped pattern on the sternum 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, and on the frons, while its gena is shiny and its supraclypeal area and frons have 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 a golden-yellow-brown. It has yellowish hair on its head, abundant golden yellow hair on its mesosoma, long, plumose, and golden hair on its metanotum, metasomal terga, and metasoma, slightly yellow, short, and fine hair on its tegula, yellow-white fringed hair on the pseudopygidial area, and a dense golden band of hair on its pronotal lobe. [10]

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 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 and 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. Its genitalia also differs from other Dialictus since its gonostylus is nearly equal in length to its gonocoxite with the additional shape and position of the hairs. [10]

Distribution and habitat

L. figueresi 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. It is found in groups of nests, similar to the American sweat bee Lasioglossum zephyrus , [11] and these groups are more numerous at higher elevations. Nests are marked by turrets made of small mud balls and are constructed during the night at the active season's beginning. A female adds to the turrets with its pygidium after bringing mud from inside the nest. When turrets are destroyed, it will only repair or replace them if the soil is soft and malleable and will not close off the entrance like some other types of bees. [3]

Nest structure

Usually found close together, the nests of L. figueresi are made up of earthen material with entrances to nests sometimes fused together. Earthen turrets, made up of small balls of mud which form a bumpy exterior and smooth interior, indicate the position of these nests, and the tunnels of these nests are almost perpendicular to the surrounding surface. Cells, coated in shiny secretions, are shortened tunnels that branch off from the main tunnel, and, once used, are normally filled up with dirt and not re-used. [3]

Colony cycle

During the lull in the wet season, from late June to early July, female L. figueresi emerge from their nests, mate, and then either establish new nests or, more rarely, re-use old nests. Heavy rains prevent much mating and foraging but some females keep extra cells open for new larvae for sporadic favorable weather during the rainy season. Nests typically contain a female and her offspring and are enlarged at the beginning of the dry season in late November and early December. Only seasonally active, females store up pollen only until mid-February and die after their first season of reproduction. During the dry season, it is more difficult to dig up the hardening soil so there is less creation of nests. Broods stay and grow in their nest. [3] By May, males and females co-exist yet don't work on the nest at this time. [1] After about 80 days, which is considerably longer than the 20 to 35 days of other halictine bees, they become young adults and leave the nest around mid-June, mating with others and starting the cycle over again. [3]

Development and reproduction

In general, female L. figueresi are mated with developed ovaries. [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 80 days, they leave the nest, mate with others, and then after preparing the next generation through the creation or re-use of nests, they die. [3]

Sexual attraction

The odors of female L. figueresi are an important stimulus for sexual attraction in males. Each female has its own unique scent. In cage experiments, male L. figueresi were more inclined towards dead females that were untreated compared to dead females that were washed in hexane, which removed their odor. The odor of females even increased the response of males to other cues. In the field, males attempted to copulate with models when paired with a female scent. These results also indicate that stimulation by sight increases with the presence of female odors. Female attractiveness is variable, and males take note of each other's preferences in choosing females. Therefore, less attractive females are less likely to mate. [12]

Mating behavior

During the characteristic lull of the rainy season, male and female L. figueresi leave their nest in order to mate. Males patrol the aggregations in an area, and when they notice a female that lands, they fly in a snake-like path towards her, pouncing on her head and causing them to fall together to the ground. There is no courtship, only copulatory vibrations that occur for various lengths of time. Additionally, males sometimes jump on other males' heads or other wasps or insects. While flying around, males are not overtly aggressive to other males. However they attempt to push off other males who are copulating with females. [12]

Learning

After continued interaction with one female, a male L. figueresi becomes less and less responsive to that female and therefore less likely to continue mating with her. This habituation shows that males learn from female odors which makes it more likely for them to mate with a greater variety of females. Additionally, males have developed the ability to learn and remember which females are responsive or nonresponsive to them, therefore decreasing the amount of time they waste on females who are nonresponsive. With their increased learning ability, they can also differentiate between receptive females and choose those who are more genetically favorable. [12]

Behavior and ecology

As solitary bees, [1] L. figueresi interact differently with the environment around them. Sometimes more than one female works on a nest, which affects the size and scope of the nest. Additionally, females have a routine that helps them become more effective at providing for their offspring. [3]

Social organization

In general, a nest contains one female L. figueresi and her offspring. In 9% to 21% of the time, two females can be found at a nest. However, there is no strong difference in size between the two females, even in comparing a mated female with an unmated female. Additionally, two-female nests contained either two mated females with developed ovarioles or one mated female with developed ovarioles and one unmated female with undeveloped ones. Having an additional female can double the amount of cells that a nest could contain, compared to other social insects which decline in efficacy as the number of individuals increases. Solitary female nests can contain up to 14 cells while two-female nests can have up to 24 cells. [3] However, the solitary nature of L. figueresi could have evolved away from eusociality. Between two unrelated females, body size was found to not be related to which bee would be more aggressive to the other, yet for bees from a reproductive time period, the female with the larger ovaries was more likely to be aggressive while the one with smaller ovaries was more likely to withdraw. Therefore, these solitary bees could still be affected by qualities of social bees as shown by their appropriate behaviors in response to other females. Additionally, females recognize bees from their own nest and are more aggressive towards those from other nests. [1]

Diel activity

Female L. figueresi begin their day around 8 or 9 AM when the temperature reaches 20–21 °C (68–70 °F). They sit at the entrance to their nest for up to 14 minutes, most likely warming up their muscles needed for flight, and then forage between 7 and 46 minutes. They can make up to 5 foraging trips a day if the weather is favorable. [3]

Interaction with other species

L. figueresi, though solitary, [1] 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. As a result, these bees have evolved defenses in response to these parasites. [3]

Diet

The diet of L. figueresi consists of balls of pollen from larvae to adults. Adult females search for and consume pollen balls made from several sources such as Melampodium divaricatum , which is unique to L. figueresi and is most likely due to its abundance in their area, Croton bilbergianus , and other Asteraceae. [3] Additionally, they stock cells with both pollen and nectar for their larvae. [1]

Parasites

The main parasite of L. figueresi is the fly Phalacrotophora halictorum . [3] The parasitism occurs during the fly's courtship behavior. After copulation, female flies enter the nest of L. figueresi when the female host is not present. Male flies continue courting the females even after initial copulation and therefore follow the female into the nest, taking it over. [13] Another potential parasite is fungi which either cause or contribute to death. Solitary female nests are as parasitized as two-female nests. [3] Other potential enemies of L. figueresi are species of Conopidae, Sphecodes , and Mutillidae. Sometimes ants invade nests and destroy brood during their scavenging. [4]

Defense against parasites

L. figueresi defend their nest from parasitism primarily by guarding the nest to prevent the flies from entering, but they also create extra, empty brood cells. [3] These empty cells cause greater difficulty for parasites in finding the larvae of L. figueresi. [14]

Related Research Articles

Bee Clade of insects

Bees are flying insects closely related to wasps and ants, known for their role in pollination and, in the case of the best-known bee species, the western honey bee, for producing honey. Bees are a monophyletic lineage within the superfamily Apoidea. They are presently considered a clade, called Anthophila. There are over 16,000 known species of bees in seven recognized biological families. Some species – including honey bees, bumblebees, and stingless bees – live socially in colonies while some species – including mason bees, carpenter bees, leafcutter bees, and sweat bees – are solitary.

Halictidae Family of bees

Halictidae is the second-largest family of Anthophila bees. Halictid species occur all over the world and are usually dark-colored and often metallic in appearance. Several species are all or partly green and a few are red; a number of them have yellow markings, especially the males, which commonly have yellow faces, a pattern widespread among the various families of bees. The family is distinguished by the arcuate basal vein found on the wing.

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

Halictus rubicundus is a species of sweat bee found throughout the Northern Hemisphere. H. rubicundus was introduced into North America from the Old World during one of two main invasions of Halictus subgenera. These invasions likely occurred via the Bering land bridge at times of low sea level during the Pleistocene epoch.

<i>Nomada</i> Genus of bees

With over 850 species, the genus Nomada is one of the largest genera in the family Apidae, and the largest genus of kleptoparasitic "cuckoo bees." Kleptoparasitic bees are so named because they enter the nests of a host and lay eggs there, stealing resources that the host has already collected. The name "Nomada" is derived from the Greek word nomas (νομάς), meaning "roaming" or "wandering."

<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.

Eusociality Highest level of animal sociality a species can attain

Eusociality, the highest level of organization of sociality, is defined by the following characteristics: cooperative brood care, overlapping generations within a colony of adults, and a division of labor into reproductive and non-reproductive groups. The division of labor creates specialized behavioral groups within an animal society which are sometimes referred to as 'castes'. Eusociality is distinguished from all other social systems because individuals of at least one caste usually lose the ability to perform at least one behavior characteristic of individuals in another caste.

Halictinae Subfamily of bees

Within the insect order Hymenoptera, the Halictinae are the largest, most diverse, and most recently diverged of the four halictid subfamilies. They comprise over 2400 bee species belonging to the five taxonomic tribes Augochlorini, Thrinchostomini, Caenohalictini, Sphecodini, and Halictini, which some entomologists alternatively organize into the two tribes Augochlorini and Halictini.

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

<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

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

  1. 1 2 3 4 5 6 7 8 Wcislo, W. T. (1997). Social interactions and behavioral context in a largely solitary bee, Lasioglossum (Dialictus) figueresi (Hymenoptera, Halictidae), 44, 199–208. Retrieved from
  2. 1 2 "Lasioglossum figueresi". Integrated Taxonomic Information System . Retrieved 28 September 2015.
  3. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Wcislo, W. T., Wille, A., Orozco, E. (1993). Nesting biology of tropical solitary and social sweat bees, Lasioglossum (Dialictus) figueresi Wcislo and L. (D.) aeneiventre (Friese) (Hymenoptera: Halictidae). 40, 21–40. Retrieved from .
  4. 1 2 Wcislo, W. T. (1991). Natural History, Learning, And Social Behavior in Solitary Sweat Bees (Hymenoptera, Halictidae). [Dissertation] Retrieved from .
  5. ↑ Schwarz, M. P. et al. (2007). "Changing paradigms in insect social evolution: Insights from halictine and allodapine bees". Annual Review of Entomology 52: 127–150. doi:10.1146/annurev.ento.51.110104.15095.
  6. ↑ Danforth, B. N. et al. (2008). "Phylogeny of Halictidae with emphasis on endemic African Halictinae" (PDF). Apidologie 39: 86–101. doi:10.1051/apido:2008002.
  7. ↑ Michener, C.D. (2000). The Bees of the World. Johns Hopkins University Press. 913.
  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. doi:10.1051/apido:2008002.
  9. ↑ Danforth B. N., Conway L., Ji S., (2003). "Phylogeny of eusocial Lasioglossum reveals multiple losses of eusociality within a primitively eusocial clade of bees (Hymenoptera: Halictidae)" Syst. Biol., 52(1), 23–36.
  10. 1 2 3 4 Wcislo, W. T., (1990). A new species of Lasioglossum from Costa Rica (Hymenoptera: Halictidae), 63, 450–453. Retrieved from .
  11. ↑ 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.
  12. 1 2 3 Wcislo, W. T., (1992). Attraction and learning in mate-finding by solitary bees, Lasioglossum (Dialictus) figueresi Wcislo and Nomia triangulifera Vachal (Hymenoptera: Halictidae). 31, 139–148. Retrieved from .
  13. ↑ Wcislo, W. T. (1990). Parasitic and courtship behavior of Phalacrotophora halictorum (Diptera: Phoridae) at a nesting site of Lasioglossum figueresi. Revista de Biología Tropical. 38(2A), 205–209. Abstract retrieved from .
  14. ↑ Tepedino, V. J., McDonald, L. L., Rothwell, R. (1979). Defense against parasitization in mud-nesting Hymenoptera: Can empty cells increase net reproductive output? 6(2), 99–104. Retrieved from .
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