This subterranean ant nests under stones or logs and in the soil, occasionally with a small mound, in clay soils, fine, sandy loam, or sandy, well-drained soils with scattered rocks, in open forests and woodlands. It is also common in New England pine barrens (Ellison et al., 2012). Lasius latipes is a temporary social parasite of Lasius americanus, Lasius crypticus, and Lasius neoniger. It has also been found nesting together with Formica occulta, Lasius sitiens and Myrmica hamulata (Mackay & Mackay, 2002).
|At a Glance||• Temporary parasite|
- 1 Photo Gallery
- 2 Identification
- 3 Distribution
- 4 Biology
- 5 Castes
- 6 Nomenclature
- 7 References
- 8 References based on Global Ant Biodiversity Informatics
The hairs on the ventral surface of the head of workers are relatively short (0.20 mm or less) and distributed over the entire surface. The hairs on the gaster are also short (0.22 mm or less) and are also scattered over the entire dorsal surface. The apex of the petiole is blunt (when viewed in profile) and convex or straight as seen from the front (rarely slightly concave). (Mackay and Mackay 2002)
Keys including this Species
- Key to Lasius-Nearctic Acanthomyops males
- Key to Lasius-Nearctic Acanthomyops queens
- Key to Lasius-Nearctic Acanthomyops workers
- Key to Lasius-Nearctic workers of Acanthomyops short key
- Key to New England Lasius
- Key to North American Lasius Species
Coast to coast in southern Canada and the northern half of the continental United States, with southern extensions to Arizona and New Mexico and to South Carolina and Tennessee.
Latitudinal Distribution Pattern
Latitudinal Range: 59.866667° to 19.14111°.
- Source: AntMaps
Distribution based on Regional Taxon Lists
Nearctic Region: Canada, United States (type locality).
Neotropical Region: Mexico.
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
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.
Wing (1968) – Of the 259 samples, 44 had data in some form relating to nest structure and location. Nests in the open numbered 25, those in woods and openings in woods 11, while the status of 8 samples was uncertain. With respect to immediate nest-cover, 19 were under stones, 3 associated with wood, 15 without immediate cover, and 7 of uncertain status. Cole (1954) listed 4 New Mexico records of Lasius latipes as A. coloradensis. The data associated with these nests indicated that they were under stones in open grassy areas with scrub oak, pine, and cedar at 7000 to 7200 feet. He listed 9 records under latipes. Of the 7 samples I have seen, 6 were latipes, and 1 coloradensis. The data associated with these samples that seem to apply to latipes is "Nests for the most part beneath stones on dry and moist, grassy, pine slopes. . . . " M. Talbot kindly sent me the 2 or 3 dozen samples that she collected in southern Michigan. The notes relating to these samples are set forth in her paper of 1963. Most nests were on the margins of fields with scattered oak trees. In many cases there was no externally visible evidence of the nest except at flight time. Some nests had immediate cover in the form of stones, wood, or mounds, the latter occurring in thick growths of grass. Kannowski (1956) discussed the structure of several nests in North Dakota; I have seen 6 of his samples. Most of the nests were in the open, under stones. In my own collecting, most nests have been found under stones either in the open, or clearings in woods, or on the borders of woods. This species is often found in sandy areas.
Annual sexual cycle The seasonal cycle of this species is typical of the other species of the genus except Lasius claviger and Lasius interjectus. It rarely nests near human buildings. The dealate queens disappear soon after nuptial flights cease. The cycle covers a relatively short, well-defined portion of the year.
During June and part of July, many of the nest records of sexual forms are based on immatures. Adult alates appear in nests from mid-July on into September. Most nuptial flights begin in late August and continue in September, with a few taking place in October.
Talbot (1963) cited August 2 as the first date for finding adult alates in nests. During a 10-year period, she observed 11 flights. They occurred in the late afternoon, often following rains. Before flights, workers opened up nests by excavation, but the time of digging out varied greatly from nest to nest. It ranged from a few days to several weeks before flight time. One colony was observed digging out on August 1, 1953, but had no real flight before September 8. However, a small number of males flew from this nest on 6 different occasions in abortive flight attempts. An estimate of the number of alates leaving a nest during a regular flight was made on September 4, 1961: the total was 2500 males and 4500 females.
Mackay and Mackay (2002), in New Mexico: Meadows and sagebrush communities, pinyon-juniper, ranging up to deciduous forests and ponderosa pine-riparian and fir forests. Nests together with Myrmica hamulata. One nest also contained Formica occulta, Lasius sitiens and Myrmica hamulata.
Ellison et al. (2012) - This species is a temporary social parasite on Lasius americanus and Lasius neoniger. The workers are generalist predators that also feed on honeydew secreted by root-feeding aphids. The enlarged front legs are used to rapidly dig a new nest. A particularly nice collection of L. latipes in the Maine State Collection was found over Labor Day Weekend in 1971, swarming in a cellar drain in Augusta, Maine.
- Check details at Worldwide Ant Nuptial Flights Data, AntNupTracker and AntKeeping.
Association with Other Insects
This species is a temporary social parasite of:
- Lasius alienus (de la Mora et al., 2021; Janda et al., 2004; Raczkowski et al., 2011)
- Lasius americanus (Ellison et al., 2012; Mackay & Mackay, 2002)
- Lasius crypticus (Mackay & Mackay, 2002)
- Lasius neoniger (de la Mora et al., 2021; Ellison et al., 2012; Janda et al., 2004; Mackay & Mackay, 2002; Raczkowski et al., 2011)
This species is a host for the ant Lasius interjectus (a temporary parasite) (de la Mora et al., 2021; Raczkowski & Luque, 2011).
The report of Lasius interjectus enslaving L. latipes by Mackay & Mackay (2002) and Janda et al. (2004) is in conflict with Raczkowski & Luque (2011) and may involve an identification error (de la Mora et al., 2021).
It has also been found nesting together with:
This species is a mutualist for the aphid Rhopalosiphum nymphaeae (a trophobiont) (Jones, 1927; Saddiqui et al., 2019).
|Worker. .||Owned by Museum of Comparative Zoology.|
Images from AntWeb
|Worker. Specimen code casent0064829. Photographer April Nobile, uploaded by California Academy of Sciences.||Owned by CAS, San Francisco, CA, USA.|
|Worker. Specimen code casent0102772. Photographer April Nobile, uploaded by California Academy of Sciences.||Owned by CAS, San Francisco, CA, USA.|
|Queen. .||Owned by Museum of Comparative Zoology.|
Images from AntWeb
|Queen (alate/dealate). Specimen code casent0102771. Photographer Jen Fogarty, uploaded by California Academy of Sciences.||Owned by CAS, San Francisco, CA, USA.|
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- latipes. Formica latipes Walsh, 1863: 311 (w.q.m.) U.S.A. Combination in Lasius: Mayr, 1866b: 889; in Lasius (Acanthomyops): Emery, 1893i: 642; in Acanthomyops: Creighton, 1950a: 431; in Lasius: Ward, 2005: 13. See also: Wheeler, W.M. & McClendon, 1903: 149; Wing, 1968: 98; Smith, D.R. 1979: 1441.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Wing (1968) – Crest of petiolar scale blunt to very blunt, convex or straight, not emarginate. Standing body' hairs numerous, more or less evenly distributed, most of moderate length. Entire surface of gula covered with 20 to 40 standing hairs, the longest of which measure 1.12 mm or more; those on dorsum of gaster measuring 0.13 mm or more. Fore femur with 12 or more standing hairs.
Standing body hairs simple to finely barbulate, usually fairly numerous on middle and hind femora. Pubescence on head and dorsum of gaster moderate, that on antennal scapes often decumbent to suberect. Body and appendages yellow to brownish yellow, surface of body at least moderately shining.
Wing (1968) – Head deformed. Scapes and funiculi extremely clavate ; antepenultimate segment of funiculus at least 2.30 times wider than long. Gula with standing hairs covering its entire surface, usually numbering 40 to 80, their maximum length 0.3 5 to 0.80 mm, usually at least 0.40 mm. FW 0.80 to 1.02 mm, FI 58 to 70, genual plates of fore femora large and conspicuous. Petiolar scale large, with crest very blunt, not emarginate. Standing hairs numerous and more or less evenly distributed over head, alitrunk, legs, and petiolar scale, which is covered by 65 to 180 hairs. Pilosity on gaster variable, .ranging from fairly sparse to dense. Pubescence on gaster dense to very dense. Body size large, AL ranging from 3.12 to 3.85 mm, with most specimens measuring at least 3.20 mm.
Standing body hairs simple to finely barbulate, usually fairly numerous on basal segment of gaster, varying on dorsum of other segments from sparse to numerous, and either (1) covering entire surface, or (2) confined to rows on posterior edges of tergites, or (3) with an intermediate pattern. Standing hairs present on hind surface of fore femora, both surfaces of middle femora, and front surface of hind femora. Pubescence on head and pronotum dilute to moderate, that on scutum and scutellum dilute, surface shining. Body color varying from blond to reddish or castaneous brown, with a few specimens fairly dark.
Wing (1968) – Antennal scapes stout, somewhat thickened apically, SL 0.70 mm or less, SI less than 70. Crest of petiolar scale blunt to moderately blunt, usually convex. Paramere with its apex usually truncate. Body size large, AL usually 1.70 mm or greater. Standing body hairs numerous. Entire surface of gula covered with 20 or more standing hairs. All femora quite pilose. Pubescence dense to moderately dense on dorsum of gaster, often suberect on antennal scapes.
Standing body hairs mostly simple, those on dorsum of gaster more or less evenly distributed. Pubescence on head, gaster, and legs moderate to dense, that on antennal scapes usually suberect. Color brown, head darker, appendages lighter.
Wing (1968) described a number of hybrid forms of this species.
Lasius murphyi × latipes hybrid
Five samples from three states: Colorado, Idaho, Iowa.
Bears a close resemblance to latipes, from which it is not now separable.
Body pilosity more dense than that of most latipes workers, otherwise no consistent differences have been noted.
Similar to latipes, but differing as follows: Standing body hairs unevenly distributed, bent, tangled, and twisted, but not matted to surface. Crest of petiolar scale more pilose. Gula with most hairs appressed. Antennal scapes and funiculi less clavate. Genual plates of fore femora less pronounced. Fore femora with hairs suberect to erect and mostly flexed, those on other femora fewer in number, mostly appressed to decumbent, and straight. SI over 70. FI 51 or less.
Pubescence on dorsum of gaster dense to moderately dense, elsewhere on body and appendages dilute to moderate. Color brown to yellowish brown.
A typical murphyi male associated with the Idaho collection indicates that this hybrid was produced by the cross, murphyi female × latipes male.
latipes × Lasius claviger hybrid
This sporadic form is recorded in a band from Minnesota and Central Illinois east to New England and New Jersey. It is by far the most common of all known hybrid taxa, most of which are known from only one or two collections.
Intermediate between latipes and claviger, but having the general appearance of latipes, from which it is not now reliably separable.
Pubescence on gaster dilute to dense. Petiolar scale variable, but usually quite similar to that of latipes. Standing hairs on gula almost invariably cover the entire surface. Length of standing body hairs and body size average and range a little greater than in latipes. Body color yellow to brownish yellow.
Intermediate between latipes and claviger. Head not or only slightly deformed. Antennal scapes and funiculi decidedly clavate; antepenultimate segment of funiculus greater than 1.55 and less than 2.30 times wider than long. Entire surface of gula covered with from 24 to 40 standing hairs, with maximum length usually less than 0.30 mm. FW 0.50 to 0.75 mm, usually at least 0.55 mm; genual plates of fore femora moderate, not conspicuous. FI 43-54. Crest of petiolar scale usually blunt to very blunt, not emarginate, rarely sharper and feebly emarginate. Scale covered with 50-75 standing hairs. Most standing femoral hairs confined to fore femora.
Pubescence on gaster from very dilute to very dense, that on rest of body usually much less dense, most of body usually shining. Pilosity on gaster variable, but most specimens have standing hairs largely confined to the posterior edges of tergites beyond first. Body color variable, most frequently a medium-dark castaneous brown. Some specimens are lighter yellowish brown, others are a dark grayish brown.
Typical of the males of latipes in all known respects.
latipes × Lasius coloradensis hybrid
When the manuscript of the present revision was nearing completion, I noted that Weber (1935) had reported collecting alpha-latipes queens on September 2, 1931 from Towner, McHenry Co., North Dakota. In this paper on Formica obscuripes, he reported on their collection as follows: "Live workers, males and dealate alpha and beta females of Lasius latipes Walsh were found in digging up an obscuripes nest at a depth of about two feet (61 cm.). They did not seem to be captive and were possibly an independent colony." Upon my request, Dr. Weber sent me a beta queen and 3 "alpha" queens, 1 lacking a head. He was unable to locate the workers and males. The study of these specimens was of particular interest, because I knew of no other alpha queens collected so far outside the known range of claviger. Claviger and coloradensis are so closely related that the previous absence of records of latipes × coloradensis seemed odd, especially since latipes × claviger is our most frequently collected hybrid taxon.
A study of these specimens showed the beta female to be a perfectly typical latipes queen. The three "alpha" females resembled latipes × claviger queens closely enough to pass for small variants of this hybrid. Assignment of these queens to latipes × coloradensis was based both on structural characters, largely metric, and the known ranges of claviger and coloradensis.
Bears a close resemblance to latipes × claviger, from which it cannot readily be separated.
Ranging and averaging smaller for most metric characters, but with AL, CI, and FI about the same, and SI higher than in latipes × claviger. Minor differences from latipes × claviger in conventional characters are: antennal scapes slightly less clavate, petiolar scale crest a little less blunt, and slight color differences. The head and appendages are light yellowish brown; the rest of the body a darker brown. Only a small proportion of the latipes × claviger queens appear bicolorous; they range and average somewhat darker than latipes × coloradensis.
Wing (1968) – Type locality: None stated. Dalla Torre (1893) cited Illinois in addition to Wisconsin (a defective queen described by Mayr, 1866) and New Jersey. Wheeler and McClendon (1903), perhaps in part because of the data in the von Dalla Torre catalogue, stated that Rock Island, Illinois was probably the type locality.
Location of types: None are known to exist despite efforts made to locate the Walsh specimens by the late William Morton Wheeler and others since the turn of the century. For this reason, I am designating a neotype queen. The neotype specimen bears 2 printed labels (Livingston Co., MICH., VIII-25-58, M . Talbot and Edwin S. George Reserve), a written code-label (238Ac-N), and a printed identification label with an added handprinted "NEOTYPE" in red. I wish to thank Dr. Mary Talbot, the collector, for giving me this typical series of latipes; it contains all 3 castes which are consistent with Walsh's descriptions. It is virtually certain that Walsh's specimens came from one of the midwestern states, although the exact locality remains in doubt. Dr. Talbot's collection made in southern Michigan almost certainly originates from the general area where the Walsh types were taken. I am depositing the neotype in the Museum of Comparative Zoology along with another queen, 2 males and 4 workers from the nest series.
- Aguilar-Méndez, M.J., Rosas-Mejía, M., Vásquez-Bolaños, M., González-Hernández, G.A., Janda, M. 2021. New distributional records for ants and the evaluation of ant species richness and endemism patterns in Mexico. Biodiversity Data Journal 9, e60630 (doi:10.3897/bdj.9.e60630).
- Boudinot, B.E., Borowiec, M.L., Prebus, M.M. 2022. Phylogeny, evolution, and classification of the ant genus Lasius, the tribe Lasiini and the subfamily Formicinae (Hymenoptera: Formicidae). Systematic Entomology 47, 113-151 (doi:10.1111/syen.12522).
- Bulter, I. 2020. Hybridization in ants. Ph.D. thesis, Rockefeller University.
- Cantone S. 2017. Winged Ants, The Male, Dichotomous key to genera of winged male ants in the World, Behavioral ecology of mating flight (self-published).
- Carroll, T.M. 2011. The ants of Indiana (Hymenoptera: Formicidae). M.S. thesis, Purdue University.
- Creighton, W. S. 1950a. The ants of North America. Bulletin of the Museum of Comparative Zoology 104: 1-585 (page 431, Combination in Acanthomyops)
- Davis, T. 2009. The ants of South Carolina (thesis, Clemson University).
- de la Mora, A., Sankovitz, M., Purcell, J. 2020. Ants (Hymenoptera: Formicidae) as host and intruder: recent advances and future directions in the study of exploitative strategies. Myrmecological News 30: 53-71 (doi:10.25849/MYRMECOL.NEWS_030:053).
- Ellison, A.M., Gotelli, N.J., Farnsworht, E.J., Alpert, G.D. 2012. A Field Guide to the Ants of New England. Yale University Press, 256 pp.
- Emery, C. 1893k. Beiträge zur Kenntniss der nordamerikanischen Ameisenfauna. Zool. Jahrb. Abt. Syst. Geogr. Biol. Tiere 7: 633-682 (page 642, Combination in Lasius (Acanthomyops))
- Ivanov, K. 2019. The ants of Ohio (Hymenoptera, Formicidae): an updated checklist. Journal of Hymenoptera Research 70: 65–87 (doi:firstname.lastname@example.org).
- Mackay, W. P. and E. Mackay. 2002. The ants of New Mexico (Hymenoptera: Formicidae). Edwin Mellen Press, Lewiston, NY.
- Mayr, G. 1866b. Diagnosen neuer und wenig gekannter Formiciden. Verh. K-K. Zool.-Bot. Ges. Wien 16: 885-908 (page 889, Combination in Lasius)
- Moura, M.N., Cardoso, D.C., Cristiano, M.P. 2020. The tight genome size of ants: diversity and evolution under ancestral state reconstruction and base composition. Zoological Journal of the Linnean Society, zlaa135 (doi:10.1093/zoolinnean/zlaa135).
- Siddiqui, J. A., Li, J., Zou, X., Bodlah, I., Huang, X. 2019. Meta-analysis of the global diversity and spatial patterns of aphid-ant mutualistic relationships. Applied Ecology and Environmental Research 17: 5471-5524 (doi:10.15666/aeer/1703_54715524).
- Smith, D. R. 1979. Superfamily Formicoidea. Pp. 1323-1467 in: Krombein, K. V., Hurd, P. D., Smith, D. R., Burks, B. D. (eds.) Catalog of Hymenoptera in America north of Mexico. Volume 2. Apocrita (Aculeata). Washington, D.C.: Smithsonian Institution Press, pp. i-xvi, 1199-2209.
- Walsh, B. D. 1863 . On the genera of Aphidae found in the United States. Proc. Entomol. Soc. Phila. 1: 294-311 (page 311, worker, queen, male described)
- Ward, P.S. 2005. A synoptic review of the ants of California (Hymenoptera: Formicidae). Zootaxa 936: 1-68 (page 13, revived combination in Lasius (Acanthomyops))
- Waters, J.S., Keough, N.W., Burt, J., Eckel, J.D., Hutchinson, T., Ewanchuk, J., Rock, M., Markert, J.A., Axen, H.J., Gregg, D. 2022. Survey of ants (Hymenoptera, Formicidae) in the city of Providence (Rhode Island, United States) and a new northern-most record for Brachyponera chinensis (Emery, 1895). Check List 18(6), 1347–1368 (doi:10.15560/18.6.1347).
- Wheeler, W. M.; McClendon, J. F. 1903. Dimorphic queens in an American ant (Lasius latipes Walsh). Biol. Bull. (Woods Hole) 4: 149-163.
- Wing, M. W. 1968a. Taxonomic revision of the Nearctic genus Acanthomyops (Hymenoptera: Formicidae). Mem. Cornell Univ. Agric. Exp. Stn. 405: 1-173.
References based on Global Ant Biodiversity Informatics
- Allred D. M. 1982. Ants of Utah. The Great Basin Naturalist 42: 415-511.
- Allred, D.M. 1982. The ants of Utah. Great Basin Naturalist 42:415-511.
- Bare O. S. 1929. A taxonomic study of Nebraska ants, or Formicidae (Hymenoptera). Thesis, University of Nebraska, Lincoln, USA.
- Borchert, H.F. and N.L. Anderson. 1973. The Ants of the Bearpaw Mountains of Montana (Hymenoptera: Formicidae). Journal of the Kansas Entomological Society 46(2):200-224
- Carroll T. M. 2011. The ants of Indiana (Hymenoptera: Formicidae). Master's Thesis Purdue university, 385 pages.
- Clark A. T., J. J. Rykken, and B. D. Farrell. 2011. The Effects of Biogeography on Ant Diversity and Activity on the Boston Harbor Islands, Massachusetts, U.S.A. PloS One 6(11): 1-13.
- Cokendolpher J. C., and O. F. Francke. 1990. The ants (Hymenoptera, Formicidae) of western Texas. Part II. Subfamilies Ecitoninae, Ponerinae, Pseudomyrmecinae, Dolichoderinae, and Formicinae. Special Publications, the Museum. Texas Tech University 30:1-76.
- Cole A. C., Jr. 1942. The ants of Utah. American Midland Naturalist 28: 358-388.
- Cole A. C., Jr. 1954. Studies of New Mexico ants. XIII. The genera Acanthomyops, Myrmecocystus, and Polyergus (Hymenoptera: Formicidae). Journal of the Tennessee Academy of Science 29: 284-285.
- Cole, A.C. 1936. An annotated list of the ants of Idaho (Hymenoptera; Formicidae). Canadian Entomologist 68(2):34-39
- 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
- Davis W. T., and J. Bequaert. 1922. An annoted list of the ants of Staten Island and Long Island, N. Y. Bulletin of the Brooklyn Entomological Society 17(1): 1-25.
- Del Toro, I. 2010. PERSONAL COMMUNICATION. MUSEUM RECORDS COLLATED BY ISRAEL DEL TORO
- Dubois, M.B. and W.E. Laberge. 1988. An Annotated list of the ants of Illionois. pages 133-156 in Advances in Myrmecology, J. Trager
- Eastlake Chew A. and Chew R. M. 1980. Body size as a determinant of small-scale distributions of ants in evergreen woodland southeastern Arizona. Insectes Sociaux 27: 189-202
- Ellison A. M., S. Record, A. Arguello, and N. J. Gotelli. 2007. Rapid Inventory of the Ant Assemblage in a Temperate Hardwood Forest: Species Composition and Assessment of Sampling Methods. Environ. Entomol. 36(4): 766-775.
- Ellison A. M., and E. J. Farnsworth. 2014. Targeted sampling increases knowledge and improves estimates of ant species richness in Rhode Island. Northeastern Naturalist 21(1): NENHC-13NENHC-24.
- Emery C. 1893. Beiträge zur Kenntniss der nordamerikanischen Ameisenfauna. Zoologische Jahrbücher. Abteilung für Systematik, Geographie und Biologie der Tiere 7: 633-682.
- Gregg, R.T. 1963. The Ants of Colorado.
- Hayes W. P. 1925. A preliminary list of the ants of Kansas (Hymenoptera, Formicidae). [concl.]. Entomological News 36: 69-73
- 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
- Ivanov, K. 2019. The ants of Ohio (Hymenoptera, Formicidae): an updated checklist. Journal of Hymenoptera Research 70: 65–87.
- Johnson R. Personnal Database. Accessed on February 5th 2014 at http://www.asu.edu/clas/sirgtools/resources.htm
- Kannowski P. B. 1956. The ants of Ramsey County, North Dakota. American Midland Naturalist 56(1): 168-185.
- La Rivers I. 1968. A first listing of the ants of Nevada. Biological Society of Nevada, Occasional Papers 17: 1-12.
- Longino, J.T. 2010. Personal Communication. Longino Collection Database
- Lubertazi, D. Personal Communication. Specimen Data from Museum of Comparative Zoology at Harvard
- Lynch J. F. 1988. An annotated checklist and key to the species of ants (Hymenoptera: Formicidae) of the Chesapeake Bay region. The Maryland Naturalist 31: 61-106
- MacGown, J.A. and JV.G. Hill. Ants of the Great Smoky Mountains National Park (Tennessee and North Carolina).
- 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.
- 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.
- Raczkowski, J.M. and G.M. Luque. 2011. Colony founding and social parasitism in Lasius (Acanthomyops). Insectes Sociaux 58:237-244
- Rees D. M., and A. W. Grundmann. 1940. A preliminary list of the ants of Utah. Bulletin of the University of Utah, 31(5): 1-12.
- Roeder K. A., and D. V. Roeder. 2016. A checklist and assemblage comparison of ants (Hymenoptera: Formicidae) from the Wichita Mountains Wildlife Refuge in Oklahoma. Check List 12(4): 1935.
- Sturtevant A. H. 1931. Ants collected on Cape Cod, Massachusetts. Psyche (Cambridge) 38: 73-79
- Talbot M. 1976. A list of the ants (Hymenoptera: Formicidae) of the Edwin S. George Reserve, Livingston County, Michigan. Great Lakes Entomologist 8: 245-246.
- Wheeler G. C., J. N. Wheeler, and P. B. Kannowski. 1994. Checklist of the ants of Michigan (Hymenoptera: Formicidae). The Great Lakes Entomologist 26(4): 297-310
- Wheeler G. C., and E. W. Wheeler. 1944. Ants of North Dakota. North Dakota Historical Quarterly 11:231-271.
- Wheeler G. C., and J. Wheeler J. 1989. A checklist of the ants of Oklahoma. Prairie Naturalist 21: 203-210.
- Wheeler G. C., and J. Wheeler. 1986. The ants of Nevada. Los Angeles: Natural History Museum of Los Angeles County, vii + 138 pp.
- Wheeler G. C., and J. Wheeler. 1987. A Checklist of the Ants of South Dakota. Prairie Nat. 19(3): 199-208.
- Wheeler W. M. 1900. The habits of Ponera and Stigmatomma. Biological Bulletin (Woods Hole). 2: 43-69.
- Wheeler W. M. 1906. Fauna of New England. 7. List of the Formicidae. Occasional Papers of the Boston Society of Natural History 7: 1-24
- Wheeler W. M. 1906. Fauna of New England. 7. List of the Formicidae. Occasional Papers of the Boston Society of Natural History 7: 1-24.
- Wheeler W. M. 1917. The mountain ants of western North America. Proceedings of the American Academy of Arts and Sciences 52: 457-569.
- Wheeler, G.C. and J. Wheeler. 1988. A checklist of the ants of Montana. Psyche 95:101-114
- Wheeler, G.C. and J. Wheeler. 1988. A checklist of the ants of Wyoming. Insecta Mundi 2(3&4):230-239
- Wheeler, G.C., J. Wheeler and P.B. Kannowski. 1994. CHECKLIST OF THE ANTS OF MICHIGAN (HYMENOPTERA: FORMICIDAE). Great Lakes Entomologist 26:1:297-310
- Wheeler, G.C., J. Wheeler, T.D. Galloway and G.L. Ayre. 1989. A list of the ants of Manitoba. Proceedings of the Entomological Society of Manitoba 45:34-49
- Wing M. W. 1968. Taxonomic revision of the Nearctic genus Acanthomyops (Hymenoptera: Formicidae). Memoirs of the Cornell University Agricultural Experiment Station 405: 1-173.
- Young J., and D. E. Howell. 1964. Ants of Oklahoma. Miscellaneous Publication. Oklahoma Agricultural Experimental Station 71: 1-42.
- Young, J. and D.E. Howell. 1964. Ants of Oklahoma. Miscellaneous Publications of Oklahoma State University MP-71
- IUCN Red List vulnerable species
- Temporary parasite
- Photo Gallery
- North temperate
- North subtropical
- Ant Associate
- Host of Lasius alienus
- Host of Lasius americanus
- Host of Lasius crypticus
- Host of Lasius neoniger
- Host of Lasius interjectus
- Host of Formica occulta
- Host of Lasius sitiens
- Host of Myrmica hamulata
- Aphid Associate
- Host of Rhopalosiphum nymphaeae
- Extant species
- Lasius latipes
- Formicinae species
- Lasiini species
- Lasius species
- IUCN Red List