Myrmecina

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Shattuck (2009) - The myrmicine ant genus Myrmecina contains 106 valid species. These are uncommon ants that are most often encountered in leaf litter samples, generally in forested areas. Colonies are small and occur in soil with or without coverings, between rocks, in twigs on the ground or in rotten wood. While little is known about their biology, some are thought to be predacious on oribatid mites, and it has been suggested that the exceptionally small heads of larval Myrmecina are an adaptation to feeding on the partially opened bodies of these mites (Masuko, 2008). A rare, social parasitic species occurs in nests of Myrmecina americana in North America (S. Cover, pers. comm.).

Identification

Shattuck (2009) - The sides of the head behind the eyes with an elongate ridge or groove on each side which starts at the mandibles, runs the length of the head and ends near the upper corners. In side view, the petiole is low, rounded and barrel-shaped and lacks a distinct node. The propodeum is armed with long spines near the angle as well as short spines or angles near the metanotal groove. The distinctive ridge on the sides of the head behind the eyes combined with the low, rounded petiole will separate these ants from all others in Australia.

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Keys including this Genus

 

Keys to Species in this Genus

Distribution

Ants in this genus are found from southern Canada south to southern Mexico, in Europe and northern Africa, and from India east to Korea and Japan and south into Fiji, the Solomon Islands and Australia. It is apparently absent from Central and South America, sub-Saharan Africa and the Middle East (Guenard, 2009). While relatively common and well represented in Papua New Guinea, this fauna is distinct from that of Australia.

Distribution and Richness based on AntMaps

Species by Region

Number of species within biogeographic regions, along with the total number of species for each region.

Afrotropical Region Australasian Region Indo-Australian Region Malagasy Region Nearctic Region Neotropical Region Oriental Region Palaearctic Region
Species 0 13 55 1 3 2 25 23
Total Species 2841 1736 3045 932 835 4379 1741 2862

Biology

Okido et al. (2020) - Members of the genus Myrmecina live in rotten wood (Wilson, 1959), soil and litter, or under stones (Ogata & Terayama, 1992). The ants are relatively rare. The biology of species of Myrmecina has been studied in only a few species. Masuko (1994) reported the predatory habits of Myrmecina nipponica and Myrmecina flava, and showed that the ants are specialized predators on oribatid mites. He concluded that the peculiarly elongate head of the larvae is associated with a feeding habit in which they insert the head into the hard oribatid body to consume the contents. The association of oribatid mites with Myrmecina was also observed in tropical Asia (Ito & Takaku, 1994; Aoki & Ito, 1997) where they show symbiosis. The colony size of the ants has been recorded in the limited number of species. Wilson (1959) noted 50 adults in a colony of Myrmecina transversa. Ohkawara et al. (1993) counted 27.4±SD 16.1 adults per colony from 108 samples of M. nipponica. Ito (1996) recorded 66±SD 24 workers and 8±SD 8.4 ergatogynes per colony from 41 samples of Myrmecina species of Java. Ergatogynes are found in some species. Emery (1916), Ohkawara et al. (1993) and Ito (1996) reported that Myrmecina graminicola, M. nipponica and undescribed species of Java have ergatogynes.

Deyrup (2015) - The diet of 2 species of Myrmecina has been studied by Masuko (1994) in Japan. These species are general predators of soil microinvertebrates that have specializations for attacking a particular type of prey, hard-bodied mites of the family Oribatidae. These specializations include serrate and scoop-shaped jaws of the worker, used for peeling open oribatid mites, and the elongate head of the larva, used for reaching into the interior of partially shelled mites. The worker mandibles of North American Myrmecina are similar to those of the Japanese species illustrated by Masuko (1994), and it is probable that North American species, also feed on oribatid mites.

Flight Period

All Flight Records for Genus

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Taxon Month Source Notes
Myrmecina americana Aug Sep Oct antkeeping.info
Myrmecina graminicola Aug Sep antkeeping.info

Life History Traits

  • Mean colony size: 24-100 (Greer et al., 2021)
  • Compound colony type: not parasitic (Greer et al., 2021)
  • Nest site: hypogaeic (Greer et al., 2021)
  • Diet class: predator (Greer et al., 2021)
  • Foraging stratum: subterranean/leaf litter (Greer et al., 2021)

Castes

Morphology

Worker Morphology

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• Antennal segment count: 11; 12 • Antennal club: 3 • Palp formula: 4,3; 3,2 • Total dental count: 7-9 • Spur formula: 0,0 • Eyes: 11-100 ommatidia • Pronotal Spines: absent • Mesonotal Spines: absent • Propodeal Spines: dentiform; present • Petiolar Spines: absent • Caste: none or weak • Sting: absent • Metaplural Gland: present • Cocoon: absent

Male Morphology

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 • Antennal segment count 13 • Antennal club 0 • Palp formula 4,3 • Total dental count 0 • Spur formula 0, 0

Karyotype

Species Uncertain

  • 2n = 66 (Indonesia) (Imai et al., 1985).

All Karyotype Records for Genus

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Taxon Haploid Diploid Karyotype Locality Source Notes
Myrmecina 66 Indonesia Imai et al., 1985
Myrmecina americana 14 Crozier, 1975
Myrmecina graminicola 14 Hauschteck, 1965; Crozier, 1975

Phylogeny

Myrmicinae
Myrmicini
Pogonomyrmecini
Stenammini
Solenopsidini
Attini

Ochetomyrmex  (2 species, 0 fossil species)

Tranopelta  (2 species, 0 fossil species)

Diaphoromyrma  (1 species, 0 fossil species)

Lachnomyrmex  (16 species, 0 fossil species)

Blepharidatta  (4 species, 0 fossil species)

Allomerus  (8 species, 0 fossil species)

Wasmannia  (11 species, 0 fossil species)

Pheidole  (1,294 species, 7 fossil species)

Cephalotes  (123 species, 16 fossil species)

Procryptocerus  (44 species, 0 fossil species)

Strumigenys  (880 species, 4 fossil species)

Phalacromyrmex  (1 species, 0 fossil species)

Pilotrochus  (1 species, 0 fossil species)

Protalaridris  (7 species, 0 fossil species)

Rhopalothrix  (19 species, 0 fossil species)

Basiceros  (9 species, 0 fossil species)

Octostruma  (35 species, 0 fossil species)

Eurhopalothrix  (55 species, 0 fossil species)

Talaridris  (1 species, 0 fossil species)

Acanthognathus  (7 species, 1 fossil species)

Daceton  (2 species, 0 fossil species)

Lenomyrmex  (7 species, 0 fossil species)

Microdaceton  (4 species, 0 fossil species)

Orectognathus  (29 species, 0 fossil species)

Colobostruma  (16 species, 0 fossil species)

Epopostruma  (20 species, 0 fossil species)

Mesostruma  (9 species, 0 fossil species)

Paleoattina

Apterostigma  (44 species, 2 fossil species)

Mycocepurus  (6 species, 0 fossil species)

Myrmicocrypta  (31 species, 0 fossil species)

Neoattina

Cyatta  (1 species, 0 fossil species)

Kalathomyrmex  (1 species, 0 fossil species)

Mycetarotes  (4 species, 0 fossil species)

Mycetosoritis  (2 species, 0 fossil species)

some Cyphomyrmex  (23 species, 2 fossil species)

some Cyphomyrmex

Paramycetophylax  (1 species, 0 fossil species)

Mycetophylax  (21 species, 0 fossil species)

Mycetagroicus  (4 species, 0 fossil species)

Mycetomoellerius  (31 species, 1 fossil species)

Sericomyrmex  (11 species, 0 fossil species)

Xerolitor  (1 species, 0 fossil species)

Paratrachymyrmex  (9 species, 0 fossil species)

Trachymyrmex  (9 species, 0 fossil species)

Amoimyrmex  (3 species, 0 fossil species)

Atta  (20 species, 1 fossil species)

some Acromyrmex  (56 species, 0 fossil species)

some Acromyrmex

Pseudoatta  (2 species, 0 fossil species)

Crematogastrini

Rostromyrmex  (1 species, 6 fossil species)

Cardiocondyla  (90 species, 0 fossil species)

Ocymyrmex  (34 species, 0 fossil species)

Nesomyrmex  (84 species, 2 fossil species)

Xenomyrmex  (5 species, 0 fossil species)

Terataner  (14 species, 0 fossil species)

Atopomyrmex  (3 species, 0 fossil species)

Cataulacus  (65 species, 3 fossil species)

Carebara  (249 species, 9 fossil species)

Diplomorium  (1 species, 0 fossil species)

Melissotarsus  (4 species, 1 fossil species)

Rhopalomastix  (14 species, 0 fossil species)

Calyptomyrmex  (38 species, 0 fossil species)

Strongylognathus  (27 species, 0 fossil species), Tetramorium  (601 species, 2 fossil species)

Cyphoidris  (4 species, 0 fossil species)

Dicroaspis  (2 species, 0 fossil species)

Aretidris  (2 species, 0 fossil species)

Vollenhovia  (83 species, 3 fossil species)

Dacetinops  (7 species, 0 fossil species)

Indomyrma  (2 species, 0 fossil species)

Crematogaster  (784 species, 3 fossil species)

Meranoplus  (93 species, 0 fossil species)

Lophomyrmex  (13 species, 0 fossil species)

Adlerzia  (1 species, 0 fossil species)

Recurvidris  (12 species, 0 fossil species)

Stereomyrmex  (3 species, 0 fossil species)

Trichomyrmex  (29 species, 0 fossil species)

Eutetramorium  (3 species, 0 fossil species)

Royidris  (15 species, 0 fossil species)

Malagidris  (6 species, 0 fossil species)

Vitsika  (16 species, 0 fossil species)

Huberia  (2 species, 0 fossil species)

Podomyrma  (62 species, 1 fossil species)

Liomyrmex  (1 species, 0 fossil species)

Metapone  (31 species, 0 fossil species)

Kartidris  (6 species, 0 fossil species)

Mayriella  (9 species, 0 fossil species)

Tetheamyrma  (2 species, 0 fossil species)

Dacatria  (1 species, 0 fossil species)

Proatta  (1 species, 0 fossil species)

Dilobocondyla  (22 species, 0 fossil species)

Secostruma  (1 species, 0 fossil species)

Acanthomyrmex  (19 species, 0 fossil species)

Myrmecina  (106 species, 0 fossil species)

Perissomyrmex  (6 species, 0 fossil species)

Pristomyrmex  (61 species, 3 fossil species)

some Lordomyrma  (36 species, 0 fossil species)

Propodilobus  (1 species, 0 fossil species)

Lasiomyrma  (4 species, 0 fossil species)

some Lordomyrma

Ancyridris  (2 species, 0 fossil species)

some Lordomyrma

Paratopula  (12 species, 0 fossil species)

Poecilomyrma  (2 species, 0 fossil species)

Romblonella  (10 species, 0 fossil species)

Rotastruma  (3 species, 0 fossil species)

Gauromyrmex  (3 species, 0 fossil species)

Vombisidris  (19 species, 0 fossil species)

Temnothorax  (512 species, 7 fossil species)

Harpagoxenus  (4 species, 0 fossil species)

Formicoxenus  (8 species, 0 fossil species)

Leptothorax  (20 species, 0 fossil species)

See Phylogeny of Myrmicinae for details.

Nomenclature

The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.

  • MYRMECINA [Myrmicinae: Myrmecinini]
    • Myrmecina Curtis, 1829: 265. Type-species: Myrmecina latreillii (junior synonym of Formica graminicola), by monotypy.
    • Myrmecina senior synonym of Archaeomyrmex: Brown, 1971a: 1.
  • ARCHAEOMYRMEX [junior synonym of Myrmecina]
    • Archaeomyrmex Mann, 1921: 448. Type-species: Archaeomyrmex cacabau, by original designation.
    • Archaeomyrmex junior synonym of Myrmecina: Brown, 1971a: 1.

Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.

Deyrup (2015) - Most of the described species live in Southeast Asia (Brown 1967) and the Australian region (Shattuck 2009), but there are several northern species that might represent a limited evolutionary radiation associated with temperate Arcto-Tertiary forests. The number of North American species is small but uncertain, in spite of analyses by Smith (1948), Brown (1949, 1951, 1967), Creighton (1950), and Snelling (1965). Brown (1967) recognized 2 species, 1 from Mexico and 1 widespread Nearctic species. A 3rd, apparently parasitic species remains undescribed (Fisher & Cover 2007), and further analysis may support reinstatement of a western species, M. californica Smith. In Nearctic Myrmecina, the chief impediment to taxonomic clarity is intraspecific variability in the widespread species M. americana Emery (Brown 1967).

Description

Worker

Eguchi, Bui and Yamane (2011) - Workers of Vietnamese species have the following features. Worker monomorphic; head in full-face view rectangular, with rounded posterior corners; preoccipital carina extending to ventral surface of head and then forming a longitudinal carina which runs anteriad; frontal carina inconspicuous; antennal scrobe absent; frontal lobe large, covering antennal insertion; median margin of clypeus raised above dorsal surface of mandibular bases, with truncate anterior margin, laterally with a submedian carina from anterior end of frontal lobe to anterior margin of clypeus; carina often forming a submedian tooth; median clypeal tooth often present but not accompanied by an isolated median seta; posteromedian portion of clypeus very broadly inserted between frontal lobes; lateral portion of clypeus often (but not always) modified into a narrow and low ridge or wall in front of antennal insertion; mandible triangular; masticatory margin with 2 distinct apical teeth followed by several teeth or denticles; antennae 11- or 12-segmented, with 3-segmented club; eye small to medium in size; mesosoma short, stout with slightly convex promesonotal dome; promesonotal suture absent dorsally; humeral angle distinct; anterior part of mesopleuron with a well developed flange projecting over base of fore coxa; metanotal groove weak or absent; propodeal spine more or less developed; an additional process or tooth sometimes present in front of each propodeal spine; propodeal lobe present only as a low carina; petiole sessile and lacking distinct node, in lateral view usually (but not always) dorsally with a triangular point or angles at or behind midlength of petiole; postpetiole in dorsal view rectangular; gastral shoulder distinct.

References