Monomorium cyaneum

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Monomorium cyaneum
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Solenopsidini
Genus: Monomorium
Species: M. cyaneum
Binomial name
Monomorium cyaneum
Wheeler, W.M., 1914

Monomorium cyaneum casent0103528 profile 1.jpg

Monomorium cyaneum casent0103528 dorsal 1.jpg

Specimen labels

Synonyms

This species normally nests under stones (or logs), but may have a simple nest in the soil, surrounded by a small mound. Brood was found in nests in June to August, sexuals were in nests in July. A dealate female was collected in August. One colony was collected together with Formica fusca, a second with Lasius coloradensis. (Mackay and Mackay 2002)

Identification

DuBois (1986) - A member of the Monomorium minimum species group. Queen Wingless; scutum and scutellum not depressed; metanotum (in lateral view) projecting to level of propodeum and scutellum; propodeum angular. Worker Propodeum angular; mesopleuron punctate; PI 29-38 (34).

Since Monomorium cyaneum has wingless queens, the following species which occur in or near its range might be confused with it: Monomorium compressum, Monomorium ergatogyna, and Monomorium wheelerorum (=Monomorium ergatogyna). Monomorium cyaneum queens can easily be distinguished from M. compressum since the latter species has a depressed scutum and scutellum, an emarginate postpetiole, and fewer than 30 erect to suberect setae projecting above the dorsal profile of the alitrunk. Monamorium cyaneum queens differ from M. ergatogyna queens since the latter species has a fringe of erect to suberect setae on the anterior edge of the scape and less facial sculpturing than M. cyaneum. Monomorium cyaneum queens are easily distinguished from M. wheelerorum queens since the latter species has an antennal fringe similar to that of M. ergatogyna queens, a flat to slightly depressed scutum and scutellum, and a notal furrow on the mesonotum.

Since the ranges of many species overlap with M. cyaneum, it is best to use the keys to separate workers which are not associated with queens. The following species are most likely to be collected within the range of M. cyaneum: M. compressum, Monomorium ebeninum, M. ergatogyna, Monomorium marjoriae, M. minimum, and M. wheelerorum. Monomorium cyaneum workers can easily be separated from M. compressum and M. ebeninum workers since the latter two species have a nonpunctate mesopleuron and more than 10 erect to suberect setae projecting from the dorsum of the alitrunk. Monomarium cyaneum workers can be separated from M. ergatogyna workers since the latter species has a more rounded propodeum and occurs mainly along the California coast. Monomerium cyaneum workers can be separated from workers of M. marjoriae, M. minimum, and M. wheelerorum since the latter three species have a nonpunctate mesopleuron and the basal face of the propodeum is longer than the declivitous face.

Keys including this Species

Distribution

DuBois (1986) - This species ranges from central Mexico (Mexican Plateau), particularly Hidalgo, Mexico, and Queretaro, east to western Vera Cruz, and west to Nayarit. These localities appear to represent the southern extent of this species. It occurs sporadically northward to southern Texas, New Mexico, and Arizona. In eastern Texas this species is apparently replaced by M. minimum which seems to prefer moister habitats than M. cyaneum. The furthest eastern collections are from the San Antonio Vicinity. The northernmost extensions of M. cyaneum occur in northern Arizona (numerous collections from Grand Canyon Vicinity). This species has been collected as far west as the Hualapai Mountains near Kingman, Arizona. Further west, M. cyaneum is replaced by M. ergatogyna, while further north, M. wheelerorum predominates. It is possible that M. cyaneum may someday be discovered in southern Utah and Nevada since the habitat is not significantly different from that of northern Arizona. It appears that while part of the sporadic distribution of this species is due to lack of collections, habitat restriction also plays a part, Most of the localities collected in Arizona and New Mexico represent upland areas (usually canyons within mountain ranges). Thus many populations may be rather isolated. At the southern extents of the range of M. cyaneum, most collections are from the Mexican Plateau. Although there are two collections from the state of Vera Cruz, both are from upland areas along the Mexican Plateau. Most collections from the plateau were near Mexico City (from such nearby states as Hidalgo and Queretaro). Collections from the western coast of Mexico are spotty. Only one collection has been made on an island (Maria Cleofas Islas, Nayarit). Three collections have been made in the region of Guaymas, Sonora and one collection in the Baja California peninsula (21 km N of La Paz).

Latitudinal Distribution Pattern

Latitudinal Range: 40.3975° to 18.56°.

     
North
Temperate 		North
Subtropical 		Tropical South
Subtropical 		South
Temperate

Distribution based on Regional Taxon Lists

Nearctic Region: United States (type locality).
Neotropical Region: Mexico (type locality).

Distribution based on AntMaps

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Distribution based on AntWeb specimens

Check data from AntWeb

Countries Occupied

Number of countries occupied by this species based on AntWiki Regional Taxon Lists. In general, fewer countries occupied indicates a narrower range, while more countries indicates a more widespread species.
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Estimated Abundance

Relative abundance based on number of AntMaps records per species (this species within the purple bar). Fewer records (to the left) indicates a less abundant/encountered species while more records (to the right) indicates more abundant/encountered species.
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Habitat

This species occurs in essentially all habitats from arid zones to grasslands, sagebrush, pinyon-pine and to wet mid altitude ponderosa pine forests, to urban habitats, it is most common in semiarid habitats. (Mackay and Mackay 2002)

Biology

DuBois (1986) - Wheeler (1914b) indicated this species nests under stones in “rather damp places on the sides of canyons.” I have observed this to be the case with colonies of this species I have collected in New Mexico and Arizona. For example, one nest of this species (Arizona: Gila Co.) was located in such a habitat on the south facing slope of a small canyon.

This nest was concealed under a stone measuring approximately 0.1m2. Most of the nest occupied an area about 10 cm in diameter, about 5 cm from the east side of the stone (a populous colony of Forelius pruinosus occupied the western portion under this stone). The portion of the M. cyaneum nest which was visible after the stone was removed consisted of a series of small chambers (1 cm in diameter) connected by tunnels (3 mm in diameter and 0.5-2 cm in length). The topmost layer of chambers was broken open when the stone was lifted. Most brood was near the surface, with different life stages clustered in separate chambers. Although this nest could only be excavated to a depth of about 7.5-10 cm due to large buried stones, I believe I collected the majority of individuals.

Colonies of M. cyaneum have multiple queens, although it is not known whether they are all functional. However, in nests I excavated, each queen was in a separate chamber and surrounded by eggs and first or second instar larvae.

Dates on which sexual forms are released are unknown, although the Gila County (Arizona) colony contained many callow queens and developing male pupae on June 12, 1979.

Monomorium cyaneum has a moderately wide altitudinal range (from 1387 m through 2286 m elevation in Arizona and from 134-1 m through 274-3 m (type locality) elevation in Mexico).

This species is a host for the ant Monomorium inquilinum (a workerless inquiline).

Castes

Worker

Images from AntWeb

Monomorium cyaneum casent0103530 head 1.jpgMonomorium cyaneum casent0103530 profile 1.jpgMonomorium cyaneum casent0103530 dorsal 1.jpgMonomorium cyaneum casent0103530 label 1.jpg
Worker. Specimen code casent0103530. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by USNM, Washington, DC, USA.

Queen

Images from AntWeb

Monomorium cyaneum casent0103529 head 1.jpgMonomorium cyaneum casent0103529 profile 1.jpgMonomorium cyaneum casent0103529 dorsal 1.jpgMonomorium cyaneum casent0103529 label 1.jpg
Queen (alate/dealate). Specimen code casent0103529. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by USNM, Washington, DC, USA.

Nomenclature

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

  • cyaneum. Monomorium minimum subsp. cyaneum Wheeler, W.M. 1914b: 43 (w.q.) MEXICO (Hidalgo).
    • Type-material: lectotype queen (by designation of DuBois, 1986: 84).
    • [Note: DuBois, 1986: 84, counted 40 workers, 4 queens in USNM, which are assumed to have paralectotype status; original description merely says“numerous” workers and queens.]
    • Type-locality: Mexico: Hidalgo, Guerrero Mill, 1913 (W.M. Mann).
    • Type-depositories: LACM, USNM.
    • DuBois, 1986: 84 (m.).
    • As unavailable (infrasubspecific) name: Emery, 1922e: 173.
    • Subspecies of minimum: Wheeler, W.M. 1917a: 501; Ettershank, 1966: 88; Kempf, 1972a: 144.
    • Status as species: DuBois, 1981: 35; DuBois, 1986: 82 (redescription); Mackay, Lowrie, et al. 1988: 91; Brandão, 1991: 357; Bolton, 1995b: 260; Mackay & Mackay, 2002: 145; Fernández, 2007b: 132.
    • Senior synonym of emersoni: DuBois, 1986: 82; Bolton, 1995b: 260.
    • Distribution: Mexico, U.S.A.
  • emersoni. Monomorium minimum subsp. emersoni Gregg, R.E. 1945b: 66 (w.q.) U.S.A. (Arizona, Texas).
    • Type-material: 79 syntype workers, 1 syntype queen.
    • Type-locality: U.S.A: Arizona, Globe, 6300 ft, iv.1937 (A.E. Emerson).
    • Type-depository: USNM (probably also in AMNH, LACM).
    • Subspecies of minimum: Smith, M.R. 1951a: 810.
    • Junior synonym of minimum: Creighton, 1950a: 219; Smith, M.R. 1958c: 128; Smith, D.R. 1979: 1382; Snelling, R.R. & George, 1979:128.
    • Junior synoynm of cyaneum: DuBois, 1986: 82; Bolton, 1995b: 261.

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

Description

DuBois 1986. FIGS. 43-56. Monomorium cyaneum. 43—Queen, lateral view. 44—Head of queen, frontal view. 45—Petiole of queen, posterior view. 46—Postpetiole of queen, posterior view. 47—Head of worker, frontal view. 48—Worker, lateral view. 49—Male, lateral view. 50—Labial palp of male. 51—Maxilla and maxillary palp of male. 52—Eighth sternite of male. 53—Ninth sternite of male. 54—Volsella of male. 55—Aedeagus of male. 56—Mandible of male. Scales: Top scale (1 mm) for Figures 43-49. Second scale (0.1 mm) for Figure 56. Third scale (0.5 mm) for Figures 52 and 53. Fourth scale (0.5 mm) for Figures 54 and 55. Bottom scale (0.1 mm) for Figures 50 and 51.

Worker

Differing from the worker of the typical form in coloration, the body being deep, metallic blue; the antennae and legs black, with the bases of the funiculi, mandibles, mouthparts, tarsi and articulations of the legs piceous.

DuBois (1986) - Head: (representing different localities; N= 10) HL 0.48-0.60 (0.51), HW 0.35-0.42 (0.39), SL 0.30-0.45 (0.35), EL 0.08-0.10 (0.09), MOD 0.05-0.06 (0.05). Structure— CI 70-83 (78), SIL 60-80 (70), SIW 77-107 (90). Pilosity—Setae erect to suberect on clypeus, frons, gular region, mandible, and occiput, decumbent to appressed on remainder. Alitrunk. Measurements PW 0.20-0.25 (0.22), PL 0.14-0.22 (0.18), WL 0.45-0.62 (0.54). Structure—Propodeum angular, basal and declivitous faces of approximately equal length. Pilosity—Dorsal outline of alitrunk with 4-8 erect to suberect setae. Sculptare—Mesopleuron covered with small, dense, non-piliferous punctures (leading to a granular appearance); lower 1/3 of side of propodeum (below spiracle) with moderate, parallel, longitudinal rugae. PI 29-38 (34). Petiole. Dorsum of node flat to slightly convex. Postpetiole: Dorsum of node flat to slightly convex. Anterior subpetiolar process absent.

Queen

Apterous, but with the thorax shaped very much as in the typical minimum though distinctly smaller and more slender. Head more shining above. Body and legs black, the latter with yellow articulations and tarsi.

DuBois (1986) - As described for Monomorium minimum except as indicated. Head: (representing different localities; N= 10) HL 0.68-0.88 (0.76), HW 0.62-0.78 (0.68), SL 0.50-0.55 (0.52), IOD 0.15-0.19 (0.18), OD 0.04-0.05 (0.05), EL 0.16-0.20 (0.18), MOD 0.12—0.16 (0.13). Structure—CI 83-96 (90), SIL 62-76 (69), SIW 70-84 (77). Scape reaching or barely Surpassing occiput. Pilosity—Setae suberect to subdecumbent near clypeus, frons, gular region, mandible, and occiput, decumbent to appressed elsewhere. Alitrunk: Measurements PW 0.41-0.48 (0.44), PL 0.28—0.32 (0.30), WL 1.28-1.38 (1.32). Structure—Mesonotum lacking notal furrow. Mesopleural suture straight with no pits at either end. Propodeum angular, basal face half as long as declivitous face. PI 22-25 (23). Wings absent (fusion of sclerites and presence of callow queens in some nests indicate queens are wingless). Pilosity—Setae suberect to decumbent on side of alitrunk. Sculpture—Small to moderate piliferous punctures evenly distributed on alitrunk (moderate punctures predominating dorsally). Petiole: dorsum of node flat. Subpetiolar process reduced. Peduncle with dense, small, nonpiliferous punctures; remainder of petiole smooth and shining with small to moderate piliferous punctures evenly distributed on anterior surface, dorsum, posterior surface, and sides. Postpetiole. dorsum of node flat. Entire surface covered with dense, small to moderate, nonpiliferous punctures. Gaster. Setae of first gastral tergite not exceeding level of dorsum of postpetiolar node. Color: Mandible yellow to yellow brown. Alitrunk brown, legs yellow brown.

Male

DuBois (1986) - Head. (representing 1 locality, N=1) HL 0.68, HW 0.72, SL 0.26, IOD 0.24, OD 0.08, EL 0.30, MOD 0.17. Structure—CI 106, SIL 38, SIW 36. Sculpture—Occiput with several moderate to large, concentric, semicircular rugae. Alitrunk. PW 0.75, FL 0.49, WL 1.72. Structure—Mesopleural suture straight (pits lacking on both ends). Metanotum (in lateral view) not reaching level of propodeum and scutellum. Pilosity—Dorsal outline of alitrunk with fewer than 30 erect to suberect setae projecting above outline. Sculpture—Scutum with large, concentric, semicircular rugae. Petiole: Dorsum of node flat. Setae erect to subdecumbent on dorsum of node. Entire surface of node covered with small, non-piliferous punctures. Postpetiole. Anterior subpostpetiolar process reduced. Entire surface of node covered with small, non-piliferous punctures. Gaster: Ninth sternite with 11 setae. Aedeagus with 18 teeth. Cuspis of volsella with 5 setae. Color. As in queen. Genitalia yellow brown.

Type Material

DuBois (1986) - Syntypic series consisting of “numerous workers and females” (Wheeler, 1914b): MEXICO: HIDALGO: Guerrero Mill [spring or summer, 1913], W. M. Mann (4 queens, 40 workers; National Museum of Natural History). Lectotype queen here designated from NMNH series bears red, handwritten label: Monomorium cyaneum Wheeler Lectotype M. DuBois 1983.

  • Monomorium minimum cyaneum: Lectotype (designated by DuBois, 1986: 84), queen, Guerrero Mill, Hidalgo, Mexico, Spring or summer, 1913, W.M. Mann, National Museum of Natural History; under stones in rather damp places on the sides of canyons.
  • Monomorium minimum cyaneum: Paralectotype (designated by DuBois, 1986: 84), 40 workers, 3 queens, Guerrero Mill, Hidalgo, Mexico, Spring or summer, 1913, W.M. Mann, National Museum of Natural History; under stones in rather damp places on the sides of canyons.
  • Monomorium minimum cyaneum: Paralectotype (designated by DuBois, 1986: 84), 12 workers, 1 queen, Guerrero Mill, Hidalgo, Mexico, Spring or summer, 1913, W.M. Mann, Museum of Comparative Zoology; under stones in rather damp places on the sides of canyons.

References

References based on Global Ant Biodiversity Informatics

  • Brandao, C.R.F. 1991. Adendos ao catalogo abreviado das formigas da regiao neotropical (Hymenoptera: Formicidae). Rev. Bras. Entomol. 35: 319-412.
  • Cover S. P., and R. A. Johnson. 20011. Checklist of Arizona Ants. Downloaded on January 7th at http://www.asu.edu/clas/sirgtools/AZants-2011%20updatev2.pdf
  • Dattilo W. et al. 2019. MEXICO ANTS: incidence and abundance along the Nearctic-Neotropical interface. Ecology https://doi.org/10.1002/ecy.2944
  • DuBois M. B. 1986. A revision of the native New World species of the ant genus Monomorium (minimum group) (Hymenoptera: Formicidae). Univ. Kans. Sci. Bull. 53: 65-119
  • DuBois, M.B. 1986, A revision of the native New World species of the ant genus Monomorium (minimum group) (Hymenoptera: Formicidae). The University of Kansas Science Bulletin 53(2):65-119
  • Fernandes, P.R. XXXX. Los hormigas del suelo en Mexico: Diversidad, distribucion e importancia (Hymenoptera: Formicidae).
  • Gove, A. D., J. D. Majer, and V. Rico-Gray. 2009. Ant assemblages in isolated trees are more sensitive to species loss and replacement than their woodland counterparts. Basic and Applied Ecology 10: 187-195.
  • Gregg R. E. 1945. Two new forms of Monomorium (Formicidae). Psyche (Cambridge) 52: 62-69.
  • Higgins J. W., N. S. Cobb, S. Sommer, R. J. Delph, and S. L. Brantley. 2014. Ground-dwelling arthropod responses to succession in a pinyon-juniper woodland. Ecosphere 5(1):5. http://dx.doi.org/10.1890/ES13-00270.1
  • Johnson R. Personnal Database. Accessed on February 5th 2014 at http://www.asu.edu/clas/sirgtools/resources.htm
  • Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
  • LaBrun, E.G. and D.H. Feener Jr. 2007. When trade-offs interact: balance of terror enforces dominance discovery trade-off in a local ant assemblage. Journal of Animal Ecology 76:58-64
  • LeBrun, E.G. 2005. Who Is the Top Dog in Ant Communities? Resources, Parasitoids, and Multiple Competitive Hierarchies. Oecologia 142(4):643-652
  • MacKay W. P. 1993. Succession of ant species (Hymenoptera: Formicidae) on low-level nuclear waste sites in northern New Mexico. Sociobiology 23: 1-11.
  • Mackay W. P., and E. E. Mackay. 2002. The ants of New Mexico (Hymenoptera: Formicidae). Lewiston, New York: Edwin Mellen Press, 400 pp.
  • Mackay, W., D. Lowrie, A. Fisher, E. Mackay, F. Barnes and D. Lowrie. 1988. The ants of Los Alamos County, New Mexico (Hymenoptera: Formicidae). pages 79-131 in J.C. Trager, editor, Advances in Myrmecololgy.
  • Miguelena J. G., and P. B. Baker. 2019. Effects of urbanization on the diversity, abundance, and composition of ant assemblages in an arid city. Environmental Entomology doi: 10.1093/ee/nvz069.
  • O'Keefe S. T., J. L. Cook, T. Dudek, D. F. Wunneburger, M. D. Guzman, R. N. Coulson, and S. B. Vinson. 2000. The Distribution of Texas Ants. The Southwestern Entomologist 22: 1-92.
  • Rosas-Mejia M., M. Vasquez-Bolanos, G. Gaona-Garcia, and V. Vanoye-Eligio. 2019. New records of ant species for Sinaloa, Mexico. Southwestern Entomologist 44(2): 551-554.
  • Vasquez-Bolanos M. 2011. Checklist of the ants (Hymenoptera: Formicidae) from Mexico. Dugesiana 18(1): 95-133.
  • Vásquez-Bolaños M. 2011. Lista de especies de hormigas (Hymenoptera: Formicidae) para México. Dugesiana 18: 95-133
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