Lasioglossum mataroa

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Lasioglossum mataroa
Lasioglossum mataroa f.jpg
Female, New Zealand, Canterbury Co. S.I., Porters Pass
Lasioglossum mataroa m.jpg
Lasioglossum mataroa unheaded male
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Halictidae
Tribe: Halictini
Genus: Lasioglossum
Species:
L. mataroa
Binomial name
Lasioglossum mataroa
Donovan, 2007

Lasioglossum mataroa is a bee species that is found in New Zealand.

Contents

L. mataroa is part of the genus Lasioglossum [1] [2] and the subfamily Halictinae. [3] L. mataroa is similar to other native bees in New Zealand, most of which are also solitary and ground nesting. [4]

L. mataroa was first described by Barry Donovan in 2007 [5]

Identification

The image of L. mataroa from Sarah McCaffrey shows the bee to scale and supports findings by Donovan that the average length of a female ranges from 4.5-6.1 mm and a male 3.9-4.9mm with widths reaching no more than 2mm. [5] Understandably due to the size the L.mataroa is also known as ‘small native bee’ and ngaro huruhuru [6] in Maori as the species is native to New Zealand. [5]

The colour of L. mataroa is primarily blackish brown with yellow antennae central and ahead of the pedicel on both sexes. The face exhibits hues of metallic reds and blues. Legs beyond the main sector of the body are yellow, but those attached to the front are half yellow and half black. [5]

Due to L. mataroa having a general resemblance to some flies they are not easily recognizable. [7] Also help separate this species from the fly the length of the forewing can be identified and ranges from 3.1– 3.9 mm on females and 2.5–3.2 mm on males. The wing veins for both are of a beige colour or pale yellow to the naked eye and L. mataroa has red tarsal claws. By sight the Halictinae can be mistaken for the Colletinae, Andreninae, and Melittidae however it can be distinguished from these families “by the strongly curved (rather than gently curved or straight) 1st abscissa (1/M) of vein M (basal vein) of the fore wing and in females by having metasomal tergum 6 hidden beneath tergum 5”. [3]

L. mataroa can be likened to the L. sordidum in many ways but they can be individually identified, either through the female of the L. mataroa being of a slightly smaller size, most commonly metallic colouration for both male and females on some of the body and as mentioned previously with the origin of the name they have a slightly longer face. [5]

Distribution

New Zealand location map.svg
Disc Plain red.svg
Lasioglossum mataroa (New Zealand)

Natural global range

L. mataroa is native and endemic [5] to New Zealand and does not appear to have been recorded anywhere else. See map image for approximate most common location for specimens collected. [5]

New Zealand range

Only found in South Island especially eastern and south-central regions possibly preferring temperate environments. [8]

Habitat preferences

L. mataroa species prefers montane environments. [5] They are a ground nesting species preferring nests sites with a silty matrix and a higher moisture content below the surface with a sloping orientation. [6] It is also important to recognize that the soils which naturally have this consistency in New Zealand have a saline content (are slightly salty) and this may therefore have a significant impact of the L. mataroa's geographical range. [5] The L. mataroa also prefers tumulus surrounding the entrance to the nest consisting of soil and can be clarified by Donovan who reports that the “Nest tunnel is about 1–2 mm across, clear, in substrate fine sandstone, soil, or silt; cells are not lined with cellophane like material”. [5]

Life cycle/phenology

L. mataroa has not widely been researched and therefore, it should be considered that information regarding the lifecycle of this species is assumed to be most similar to Lasioglossum sordidum as confirmed by Donovan, “An outline of the life cycle is known for only one species, L.sordidum, but that of other species is almost certainly similar”. [9] Depending on climatic conditions particularly in relation to soil temperature early summer November – December is generally the period when new adults emerge from the nest. If soil is warming much earlier than this then emergence could even begin in late winter. Ground nests are close together and therefore there could be many thousands emerging at the same time. [9] The percentage of male and female individuals hatching may have been altered in the nest as the female bee is partly able to influence the ratio of sexes. [10] The ability to influence sex ratio for Hymenoptera is due to the haplo-diploid system whereby the unfertilized eggs produce males and fertilized eggs produce females, this leaves the ability for speculation whether the female L. mataroa considers the needs for the success of its own species in its local population when mating. Once out of the nest active flight season begins immediately and the female bees start to construct their own nests.

With preference to nesting alongside each other, [4] mature L. mataroa may re-use a previous nest, one which they have spent the winter in or build a new one. [5] Males do not play an active role in the nesting cycle and therefore, the males only role is to feed himself, seek a female mate, and rest, “males which appear by late spring are all gone [die] by autumn” (B. Donovan, personal communication, March 26, 2019). Females undertake all nest construction, defence, raising of young and foraging to feed young. Females also bear the responsibility for the collection of pollen and nectar which is primarily transported on the hairs of metathoracic legs and propodeum. [5] Furthermore, a female born in late summer or autumn that has been fertilized will spend the winter underground in the nest possibly living for up to 12 months or more. However, as B. Donovan (personal communication March 26, 2019) explained it may be possible that those bees over wintering in the nest may die and be replaced by the fertilized daughters resulting in the life span being like that of the male.  

The L. mataroa nest construction is a blind tunnel excavated in fine-grained moist soil that contains cells in which the larvae are raised. The cells contain individual chambers in which the female bee will instil mass-provisions of pollen and nectar that are necessary for the survival of the larvae. The cell is sealed after the egg has been laid on the provisions and the female bee does not re-enter. Although this species generally has only one brood of offspring per year, if the summer has been particularly hot it is possible that a second brood may be nested. [5]

Diet and foraging

Pollen and nectar is consumed by all New Zealand bees, [5] protein is gained through the pollen and sugars are gained through nectar.  

The Halictinae have a long resting period throughout winter, so it is necessary to build up resources and reserves to last throughout therefore they must forage on a wide variety of flowering plant species to gain maximum provisions. Host plants of this species include natives and introduced, [5] but L. mataroa has a liking “for 3 native species of Asteraceae, but a very strong preference for 2 introduced species in the family”. [11] The daisy family, Asteraceae, are the largest of flowering plants (Stevens, 2001 as cited in Panero & Crozier, 2004), [12] and L. mataroa prefers the Achillea millefolium (Yarrow) which is highly competitive possibly making it readily available to forage on and “commonly found in pastures throughout New Zealand” [13] but it is also resistant to drought in the summer. [13] The Taraxacum officinale (Dandelion) is the second and is also commonly found in pastures but those that are low in competition as it grows in soil which has fairly low soil fertility. [14] This could possibly explain why the L. mataroa favours this plant as nesting sites are in saline soils and therefore the dandelion species would be growing close by and easily accessible. Furthermore, the root system of these plants reach deep under the surface allowing the plant to survive drought which would be common conditions in the temperate inland environment [13] where the bee can be found.

Predators, parasites, and diseases

No information found for L. mataroa gave specific details for predators, parasites or diseases.

"Enemies of Halictinae are unknown" (Donovan, 1980, p. 107). [8]

Cultural Value

The origin of the name mataroa in Māori breaks down to mata (face) and roa (long). This is due to the females’ face appearing longer than other species in the genus. [5]

Economic value

Native bees play an important role in commercial crops of New Zealand. They are pollinators of some fruits of great commercial value like kiwi fruit. [15] Not being affected by varroa mites makes them easy to control. [15]

Related Research Articles

Halictidae Family of bees

Halictidae is the second-largest family of 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>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.

<i>Anthidium manicatum</i> Species of bee

Anthidium manicatum, commonly called the European wool carder bee is a species of bee in the family Megachilidae, the leaf-cutter bees or mason bees.

<i>Colletes hederae</i> Species of bee

Colletes hederae, the ivy bee, is a species of plasterer bee belonging to the family Colletidae subfamily Colletinae.

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>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>Leioproctus fulvescens</i> Species of bee

Leioproctus fulvescens is a species of bee native to the South Island of New Zealand. Adults are about 10 mm long with dense characteristically yellow to orange-brown hair; this feature distinguishes them from other New Zealand Leioproctus species, which have white to cream hairs. The bees fly primarily in the spring and summer, with the majority of individuals between November to March, though some have been observed as early as September.

<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 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.

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>Macropis nuda</i> Species of bee

Macropis nuda is a ground nesting, univoltine bee native to northern parts of North America. Thus, this species cocoons as pupae and hibernates over the winter. The species is unique as it is an oligolectic bee, foraging mainly for floral oils from Primulaceae of the genus Lysimachia.

<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>Colletes validus</i> Species of bee

Colletes validus, colloquially known as the blueberry cellophane bee or blueberry polyester bee, is a solitary, specialist bee in the family Colletidae. It is found primarily in eastern North America where it nests in sandy soils near ericaceous plants.

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

Lasioglossum sordidum, also referred to as the small native bee, is one of the smallest native bees found in New Zealand.

A list of the species of Hymenoptera from New Zealand; currently listing the 'stinging wasps' (Aculeata), which includes ants, bees, and social wasps.

<i>Leioproctus boltoni</i> Species of bee

Leioproctus boltoni is a species of bee in the family of plasterer bees. This species was first described in 1904 and is endemic to New Zealand. They are a solitary bee, small and black in appearance. L. boltoni can be found throughout the main islands of New Zealand and forages on the flowers of both native and introduced species of plants. This species nests in the soil with their life cycle lasting approximately a year.

Leioproctus huakiwi is a species of bee in the family Colletidae family. This species was first described in 2007 and is endemic to New Zealand. L. huakiwi is a solitary bee, small and mainly black in appearance. It nests in the ground in bare, dry and fine soil. This species has been the subject of a successful translocation in Canterbury in 2005.

References

  1. Gibbs, J; Brady; Kanda; Danforth (2012). "Phylogeny of halictine bees supports a shared origin of eusociality for Halictus and Lasioglossum (Apoidea: Anthophila: Halictidae)". Molecular Phylogenetics and Evolution. 65 (3): 926–39. doi:10.1016/j.ympev.2012.08.013. PMID   22982437.
  2. Ascher, J; Pickering (2011). "Discover Life bee species guide and world checklist (Hymenoptera: Apoidea: Anthophila)".
  3. 1 2 Agriculture Canada (1993). Hymenoptera of the world: An identification guide to families. Ottawa, Canada: Canada Communication Group - Publishing. p. 318. ISBN   0-660-14933-8.
  4. 1 2 Hart, N. (2016). Monitoring New Zealand's native bees: a collaborative approach using image analysis. . Auckland University of Technology
  5. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Donovan, B.J. (2007). Apoidea (Insecta: Hymenoptera) (PDF). Fauna of New Zealand. 57. Lincoln, New Zealand: Manaaki Whenua Press. ISBN   978-0-478-09389-6.
  6. 1 2 Hart, N (n.d.). "Native bees - ngaro huruhuru" . Retrieved 15 March 2019.
  7. Manaaki Whenua, L.R. (n.d.). "FNZ 57 - Apoidea (Insecta: Hymenoptera) - popular summary".
  8. 1 2 Donovan, B.J. (1980). "Interactions between native and introduced bees in New Zealand" (PDF). New Zealand Journal of Ecology. 3: 104–116.
  9. 1 2 Donovan, B.J. (2007). Apoidea (Inescta: Hymenoptera) (PDF). Fauna of New Zealand. 57. Lincoln, New Zealand: Manaaki Whenua Press. p. 22. ISBN   978-0-478-09389-6.
  10. Goodman, L.J.; Fisher (1991). The behaviour and physiology of bees. Wallingford, UK: C.A.B International. ISBN   0-85198-721-4.
  11. Donovan, B.J. (2007). Apoidea (Inescta: Hymenoptera) (PDF). Fauna of New Zealand. 57. Lincoln, New Zealand: Manaaki Whenua Press. p. 125. ISBN   978-0-478-09389-6.
  12. Panero, J; Crozier (2004). "Asteraceae".
  13. 1 2 3 Massey University (2016). "Yarrow".
  14. Massey University. "Dandelion".
  15. 1 2 Hart, N (2007). "Industrious native bees: a case study in Whangarei" (PDF).