This is a common, widely distributed species. Nests are found in the soil (often under stones) and often adjacent to the nests of other species, where it steals food or brood from its host. Specimens have been collected from subterranean, surface and vegetation Vienna sausage bait traps, as well as surface, subterranean and vegetation fire ant bait traps. It is commonly collected in pitfall traps. Reproductives and brood are present throughout the summer. This is also a household pest, although it may not be noticed due to its small size. It hollows out seeds, thus destroying seed in beds. Colonies contain up to a few thousand workers. Sexuals are found in nests from July to October. Nuptial flights occur from late July to early fall, individuals mate in the air. These ants are predaceous, but are also omnivorous (feeding on seeds) and eat dead insects. They also tend Homoptera. (Mackay and Mackay 2002, Pacheco and Mackay 2013)
|At a Glance||• Facultatively polygynous|
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Pacheco and Mackay (2013) – Worker - This is a small, yellow species (occasionally pale brown), in which the dorsum of the head is finely punctated. The lateral clypeal teeth are well developed while the extralateral teeth are developed into small bumps. The minor funicular segments are typically about 0.14 mm in length. Queen - The queen is moderately large at just over 5.00 mm in total length and concolorous yellow to pale brown. The head and dorsum of the mesosoma are semi-coarsely punctate, with long yellow erect hairs projecting from them. The petiole and postpetiole are horizontally striated. The petiolar peduncle has a small flange ventrally. Male - The male is concolorous dark brown to bicolored with a brown head and gaster and yellow to golden brown body and is moderately large at just under 4 mm in total length. The anterior clypeal margin is convex. The frontal lobes are horizontally striated. The propodeum, petiole and postpetiole are horizontally striated. The petiolar peduncle has an angle ventrally (not a tooth or flange).
As most thief ant species are minute and concolorous yellow in color, it is difficult to differentiate S. molesta from other small species. It is often the case that any small, yellow species is incorrectly named S. molesta. However, Solenopsis molesta is the most common and widespread thief ant in the continental United States. When one collects a small, yellow Solenopsis, there is a high probability it is S. molesta.
This common species can be separated from Solenopsis texana, Solenopsis carolinensis and Solenopsis abdita, by the longer length of the minor funicular segments. It can be separated from Solenopsis krockowi and its relatives, as the punctures on the head are much finer and the minor funicular segments are rarely greater than 0.150 mm in total length. It is difficult to separate the worker of Solenopsis validiuscula. Solenopsis molesta workers are often smaller than those of S. validiuscula (total length 1.80-2.00 mm). The cephalic punctures of S. validiuscula are moderately coarse, while S. molesta are finer. If queens are available, the queens of S. validiuscula are always dark brown, while S. molesta is typically concolorous yellow. The male of S. molesta is light brown and occasionally bicolored, while the male of S. validiuscula is concolorous dark brown. The pedicel of the male of S. molesta is large compared to that of the S. validiuscula male (length nearly as long as the scape). Although the two species are similar in size and form, based on the above differences in the castes, they will be recognized as different species.
It is difficult to separate the workers of S. molesta from S. texana. Solenopsis texana is consistently smaller, with the total length ranging from 1.20-1.30 mm. The queens of S. molesta are easily separated as they are much larger than those of S. texana (total length of S. molesta ranging from 4 - 5.5 mm, the queen of S. texana has a total length of slightly over 3 mm). The queen of S. molesta is yellow or pale brown; that of S. texana is black to dark brown.
The worker is easily confused with those of Solenopsis salina, as both species are yellow and have similar cephalic punctures. They can be separated as the minor segments of the funiculus of S. molesta are nearly always over 0.120 mm in length, those of S. salina are nearly always shorter than 0.100 mm in length. The clypeal teeth of S. molesta are nearly straight, whereas they are usually slightly incurved in S. salina.
Keys including this Species
A wide range that includes southern areas of Canada, most of the continental US and northern Mexico.
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
Solenopsis molesta nests underground, often under stones, generally near the nests of other species where it steals from its host. Solenopsis molesta has been collected in nests of the following species, Myrmica americana, Manica invidia, Pogonomyrmex occidentalis, Pogonomyrmex montanus, Veromessor lobognathus, Monomorium minimum, Pheidole bicarinata, Pheidole pilifera, Dorymyrmex insanus, Camponotus vicinus, Lasius crypticus, Lasius neoniger, Lasius sitiens, Lasius umbratus, Lasius claviger, Lasius interjectus, Lasius murphyi, Formica argentea, Formica neogagates, Formica limata, Formica rubicunda, Formica bradleyi, Formica altipetens and Formica fusca. Colonies contain up to a few thousand workers. Reproductives and brood are present throughout summer to fall. It is occasionally polygynous, with up to eight queens in a single nest. Nuptial flights occur from late July to early fall. (Mackay and Mackay 2002, Pacheco and Mackay 2013)
Hayes provided an extensive accounting of this species in a 1920 publication. His studies were motivated by this ant being a troublesome pest species. The following is selected text from this work:
Seeds as Food The ravages of this versatile little ant on the planted seed of sorghums are much the same as in the damaged fields of corn. Forbes (1894, p. 10) describes the injury to corn as follows:
In the corn field these ants were usually collected about the kernels in the earth, and frequently more or less hidden in little cavities excavated in the softened grain. May 19, 1887, they were very abundant in a field of corn in sod in Champaign county, eating out the planted kernels. In autumn the same species has been detected by us indulging a similar appetite but in a way to do no harm. September 11 to 21, 1893, it was found feeding on and within the kernels of corn at the tips of ears, which had evidently been injured previously by crickets and grasshoppers. The solid substance of the grains is not actually eaten by these ants-a fact which I demonstrated by dissection of the ants-but it is simply gnawed away, doubtless for the sake of the sweetish and oily fluids of the softened kernels. If plants start from seed thus injured, they are shorter than others adjacent, and have a stunted, weak appearance.
Wheeler (1910, p. 268) states that Solenopsis geminata is the only species of the tribe Solenopsidii that is granivorous. However, on a following page (p. 427). quoting Forbes, he mentions X. molesta as eating the kernels of maize and again (p. 269) he states that Solenopsis rufa stores seed in its nest. Say (loc. cit.) first reported the species as an enemy of garden seed. The writer has found the species feeding on planted seed of the following sorghums: Kafir, cane, milo, and feterita. Workers often gather in the fall under corn piled on the ground where they gnaw on broken kernels.
Hayes (1920) Table 1.
|July 20 (b)||216||34||74||12|
|July 28 (c)||336||247||78||1||1|
(a) not counted (b) one winged queen found (c) four winged queens; two winged males and seventy-three larvae and pupae of sexual forms found
Egg Incubation The length of the period was found to vary from 16 to 28 days, depending on temperature and moisture conditions. Daily egg-laying records of eight queens were kept for a period of 16 days by removing from the nest eggs laid during each day. The average number of eggs laid for the period was 103.3. The greatest number from one individual was 387 and the smallest was 27. One queen deposited 105 eggs in a single day.
Larval Stage The length of the larval stage is highly variable, depending on weather conditions to a marked degree. During midsummer, larvæ were reared to the semipupal stage in 21 days. In another instance, a single larva was under observation from October 10 to May 12 when it transformed to the semipupal stage.
Larval Feeding Larvae are fed regurgitated food by the workers. Workers, in artificial nests, were often seen to place small bits of crushed kafir seeds and torn parts of their larvae and pupae on the bodies of the young near the mouthparts where the larvae were seen to bite them. Larvae were frequently observed, while lying on their back, to straighten out their curved body. These movements are repeated at short intervals and the mandibles open at each up movement and close on the down-movement. These moving larvae were generally fed at once, or soon after making these apparent supplications.
As the larva becomes full grown, a large undigested meconium is voided from the alimentary tract. Workers were seen at times aiding the larva to get rid of this mass by tugging at it while it was being cast off. This change marks the end of larval development and the beginning of the semipupal stage. Large larvæ have often been encountered in nests of this species, which were, undoubtedly, either larvae of males or queens. None were ever reared to maturity in artificial nests. Except for their
much greater size, they resemble the worker larvae, and upon reaching their final stages of growth undergo similar changes to the semipupal stage. In this stage, they are not greatly unlike the larvæ except for the absence of the black mass in the abdomen. The semipupal stage was found in midsummer to vary from 2 to 11 days.
Worker Pupae The comparative size of the worker, the queen and the male pupae is shown in figure 8. When this stage is reached in their development, the sex of the individuals can easily be distinguished by their size.
The worker pupae (fig. 9) are about 1.5 to 1.8 mm. long. When freshly transformed from the larval stage, they are pearly white in color, but as development proceeds, they darken through a creamy white to a pale yellow, and later to a darker yellow which is much the same as the color of the adult worker. The length of the worker pupal stage was found to be from 13 to 27 days. The same period for the males and queens has not been determined.
Queen Pupa The female pupae are larger than the worker pups, measuring about 4.5 mm. long. They are also considerably larger than the pupae of the males. At first, the queens are pearly white, but as development proceeds, they color much the same as the workers. When ready to transform to adults, the queens molt, being greatly assisted in the process by the workers of the colony.
The pupae of the males are intermediate in size between the worker and queen pupae, being 3.5 to 3.6 mm. long. From a whitish color similar to that of the other pupae, this sex develops to a much darker color, being nearly black. By their size and this black color, they are easily distinguished from the others. Some time previous to their last transformation, the males, as well as the females, develop rather prominent wingpads. Pupae of the males and queens are not found in the colonies until
early in July. They frequently occur in fairly large numbers and are well cared for by the workers.
Callow Stage The newly hatched ant, before it has attained its full adult coloration, is called a callow. Except for this lack of color, the callow is almost the same in appearance as the adult workers. At first it is helpless and clumsy and must be cared for by attendant workers, which often carry it about when the need for transportation arises. Callows are even fed by the workers. As they become older and stronger they gradually darken to the adult color and are more and more neglected by the workers until at last they become entirely independent. The coloration, which is due to the deposition of chitin and perhaps some pigment, will take place in two days; that is, in less than two days one cannot distinguish the younger from the older individuals.
Development Time The minimum length of the egg stage was found by the method just described to be 16 days; the larval stage 21 days; the semipupal stage 2 days; and the pupal stage 13 days. Assuming the total of these figures as a probable minimum time required for development of workers, we have 52 days as the least time in which they will mature. The maximum time for development, due to the fact that larvae, will live over the winter, is subject to much variation. The longest time for eggs to hatch was found to be 28 days. As mentioned above, larvae will develop in 21 days. This is in midsummer. Others will live through the winter. A single larva was under observation from October 10 to May 12, when it transformed to the pupal stage. The maximum length of the semipupal stage was found to be 11 days, and that of the pupal period proper was 27 days.
Adjustment to certain limited habits seems not to be the rule with the species concerned, at least, not in the localities of Kansas where the ant has been studied. Their wide and varied distribution in such diverse habitats as houses, pastures, meadows, prairies, or plowed fields seems to indicate no especially desired abode. The nature of the soil seems not to be of extreme importance, as colonies are found in heavy clay soils, light sandy soils, or many intermediate gradient types. The colonies are found in almost all situations of this region.
The nest consists of random burrows through the soil, scarcely more than 1 millimeter in diameter, which frequently enlarge to form chambers from 10 to 15 millimeters in diameter. In these large chambers, the brood is reared. Often the one or more openings of a colony under a stone will be greatly enlarged a t the surface of the soil to form brood chambers where the young can be taken, when the soil becomes saturated from rains, to receive the warmth of the sun through the protecting stone. The following field note describing a colony may be regarded as a typical example of a colony:
A large colony of ants was taken under a stone 18 by 12 by 6 inches in a pasture near the State School, Winfield, Kan. At the opening of the nest, there were two entrances; one was nearly round and the other was oblong oval. Several hundred workers were gathered near a large pile of larvae grouped in the round entrance. About 200 workers were on the under surface of the stone when it was turned over. One-half inch below the round entrance about 100 larvae were taken. Tunnels could not be traced from here, but at a depth of 1 1/8 inches a tunnel was found that went south for 4 inches at the end of which were about 3000 larvae. These larvae were in a chamber about one-half of an inch in diameter. Directly below this room at a depth of 2 ½ inches from the surface, a tunnel went north for 3 inches and ended in a chamber containing about 200 larvae. Down 3 inches, a tunnel was followed in an easterly direction of 1 ½ inches where it divided, one branch going directly east while the other went downward and in the same easterly direction for 2 inches. At the end of each were large chambers containing piles of larvae. Workers and larvae were scattered throughout the tunnels. No evidence of food being stored was found. No queen was found.
This colony was taken in early spring and contained no eggs or puae. Otherwise, the colonies examined later in the season do not differ much in their general aspects.
Associations with other Organisms
It is not impossible, as supposed in the case of Solenopsis fugax, that isolated nests of S. molesta may be connected with nests of other ants by long underground galleries. It is perhaps by this hypogæic mode of travel that the workers are able to find and devastate fields of planted sorghum seed.
This species is often found under stones with colonies of other ants. The two colonies are connected by small galleries forming what are called compound nests. These small tunnels ramify through the workings of the larger ants. The minuteness of the galleries prevents the larger species from molesting the small invaders who, with comparative safety, forage at will.
Wheeler (1901, p. 533) reports S. molesta living in lestobiotic relationship with the following ants: Pachycondyla harpax Fabr., Odontomachus clarus Roger, Camponotus sansabeanus,Camponotus festinatus, Formica, Lasius, Stenamma, and Myrmica. Forbes (1908, pp. 38, 41-42.) records it living in harmony with Lasius niger-americanus Emery, and King (1896, p. 169) with L. niger Linn. Other ants with which it has been found are: Ponera pennsylvanica (King 1896, p. 169), Camponotus americanus Mayr (King, 1895, p. 221), Lasius interjectus Neyr. (King 1895, p. 222), L. claviger Rog. (King, 1895, p. 222), Prenolepis parvula Mayr (King, 1896, p. 170), P. imparis Say (Mann, 1911, p. 30), Myrmica lobicornis Myl. (King, 1856, p. 170), Tapinoma sessile Say (Mann, 1911, p. 30), Pheidole californica Mayr (Mann, 1911, p. 30), Camponotus maccooki Forel (Mann, 1911, p. 30), C. maculatus vicinus Mayr (Mann, 1911, p. 30), Formica fusca Linn. (King, 1896, p. 169), F. fusca var. subsericea Say (King, 1896, p. 169), Aphaenogaster fulva Rog. (King, 1896, p. 170), Formica pallisle-fulva subsp. nitidiventris Em. (King, 1896, p. 169), F. cinerea Mayr (Wheeler, 1902, p. 952) and the termite, Termes flavipes (King, 1895, p. 220). In this investigation, S. molesta was taken in colonies of Iridomyrmex pruinosus var. analis Ern. Andre, Cremastogaster lineolata var. punctullata Emery, Hypoponera inexorata, Pheidole sp., and the termite, Leucoterms lucifugus Rossi.
Among those that live in the nests are two myrmecophiles reported by Schwarz (1890, p. 241; 1890, pp. 244 and 247), a species of Lithocharis, and a species of Myrmecochara. Other insects that have been reported found in the nests are Atheta exilissima Casey (Wickham, 1894, p. 80). Rhyssemus sonatus Lec. (Wickham, 1892, p. 322) (possibly accidental), Isobrachium Myrmecophilum Ash. (Mann, 1911 p. 29). Aleocharini g. et sp. (King, 1897, p. 102), and Auxopaedeutes sodalis Brues (Brues, 1903, p. 127). Dactylopius sp., a mealy bug, was found repeatedly in the nests of S. molesta in Kansas, this being the only true inquiline observed. When so found, there are generally a number of grass roots in the soil near the nests where the mealy bugs can get their nourishment. Workers will pick up these guests as they do with their own young and carry them to places of safety when danger threatens, Other types of associates are those upon which the ants are in attendance, such as aphids and scale insects; while still another group includes those upon which the ant preys.
This ant has varied habits. As a beneficial predaceous insect it receives perhaps as much prominence as it does as a pest. The beneficial aspect is manifested by the activities of the ant in attacking many of our other pernicious pests. A glance at the accompanying list of species which S. molesta attacks will serve to show the ant's usefulness. The names in the list without references are from original observations.
Insect species known to be attacked by S. molesta are as follows:
- Grape curculio, Craponius inæqualis (Brooks, 1906, p. 241)
- Walnut curculio, Conotrachelus juglandis (Brooks, 1910, p. 182).
- Cotton boll weevil, Anthonornus grandis (Pierce, 1912, p. 41).
- Chinch bug (eggs), Blissus leucopterus (Headlee and MeColloch, 1913,
- Codling moth, Carpocapsa pomenella (Brooks and Blakeslee, 1915,
- Maize billbug, Sphenophorus maidis.
- Corn stalk borer, Papaipema nitella.
- Corn earworm, Chloridea obsoleta.
- Hessian fly, Mayetiola destructor.
- Grasshopper (eggs), Acrididæ (different species).
- Ladybird beetle, Megilla maculata.
- White-marked tussock moth, Hemerocampa leucostigma.
- Scarabaeidae, Ligyrus relictus.
- Larger ants.
- Other colonies of S. molesta.
The amount of damage which this species inflicts on crops and its noxious character in kitchens is somewhat compensated for by predaceous habits. Unfortunately, the ant does not appear to be of material value as an enemy of any of the species mentioned in the list for in most, if not all, cases the report of molesta as an enemy of various insects comes from isolated and, perhaps, chance observations. In the opinion of the writer, many of these cases arise when the ants find an injured or helpless victim that is incapable of defense, or it is even possible that they attack their victim after it has died. These reasons, combined with records of the ant feeding on fats, grease, and cured hams, might lead to the conclusion that many of the accounts of molesta as a predaceous enemy are only instances of the ant's scavenger habits.
The known enemies of S. molesta are few and of widely different kinds. Spiders often trap the workers in their webs. Two other ants, Crematogaster lineolata and soldier ants of Pheidole pilifera, were observed killing workers. The common horned toads (Phrymoma cornutum Harlan), upon examination of their stomach contents, were found to have eaten numbers of S. molesta workers. In the stomach of a skunk (Eumeces sp.), one S. molesta worker was found. A small mite (Hypaspis sp.), which is probably ectoparasitic, was repeatedly taken on workers, queens, and eggs. West (1910, pp. 14-22) found S. debilis in the stomachs of two moles. No endoparasites are known.
The following birds are known enemies of S. molesta: English sparrows, bank swallows, barn swallows, chipping sparrows (Judd, 1902, pp. 33-34), flicker (Beal, 1911, p. 56) and the kingbird (Beal, p. 16, and Judd, loc. cit.).
This species is a prey for the tiger beetle Tetracha virginica (a predator) in United States (Valenti & Gaimari, 2000; Polidori et al., 2020).
Agriculture When first reported, Say (1836, pp. 293-294) stated that the species attacked garden seed, whether the seed was planted of not he fails to mention. The next reference, by Fitch (1856, pp. 129-130), reports the ant so numerous in the fields as to threaten to cut off every blade of corn by gnawing the tender leaves “for the purpose of drinking the sweet juice which flows from the wounds.” Forbes (1884, p. 45) found this insect, which he called Solenopsis fugax, in great numbers in sorghum and broom-corn fields, where he noted they were paying no attention to the superabundant plant lice. They were also observed (Forbes, 1884, pp. 61; 112-113) gnawing out the fleshy fruit of strawberries and hollowing out planted seed corn. As Solenopsis debilis Forbes later (1894, pp. 8-10; 66; 69) noted further injury to corn, both in the ground and in ears of standing corn which had been previously injured by crickets and grasshoppers. Workers were several times noted in attendance on the corn root-louse, Aphis maidi-radicis Forbes, and a minor aphid of the corn plant, Geoica squamosa Hart. Hunt (1886, p. 58) lists both S. fugax and S. molesta as enemies of corn.
Webster (1890, pp. 257-258) observed this ant attending a species of Dactylopius on red clover. Workers were seen carrying away the substance of seed corn after it had been planted. He also described them (1893, p. 158) as injuring blackberries, concerning which he says “their attacks upon ripe fruit is exceedingly annoying, as their diminutive size prevents their being readily discovered.” Felt (1915, pp. 68-69) found the species injuring corn a t Salt Point, N. Y. In this instance, recently planted corn seemed to be “growing smaller” and it was found that the ant was eating the interior out of the kernels as described by Forbes. The development of the plants was arrested and they appeared to become smaller.
As a field pest in Kansas, the chief damage consists largely of the destruction of seeds of kafir, cane, milo, feterita, and corn (maize) soon after they are planted. Injury to the sorghums is much the same as that described by other workers in the case of corn, concerning which Forbes (1894, p. 9) writes, “a kernel may be found wholly or partly hollowed out, the mealy interior being not devoured, but scattered about in the earth, while the cuticle or outer shell of the seed remains but little disturbed.”
During the past few years, thousands of acres of sorghum crops have had to be replanted from one to six times because of the ravages of this ant and in a number of cases it has been impossible to get a good stand. With seed at $3 per bushel, as it was during the season of 1914, this means a considerable monetary loss as well as time and labor spent in replanting. A few of the following records from field notes and correspondence will serve to show more vividly the amount of damage done by this pest.
May 7, ’12, Milton Clegg, Neodesha, reported that ants destroyed 40 acres of cane and kafir.
May 12, ’13, A. T. Sharp, Council Grove, reported ants injuring listed kafir.
June 18, ’13, E. W. Dales, Eureka, had 100 acres in cane and kafir, but because of the ants only 25% germinated.
Feb. 10, ’13, Chas. C. Crane, Longton, writes that on account of the ants most of the farmers in his neighborhood were compelled to replant several times last year, and some did not, even then, get a stand.
June 27, ’12, B. P. Cunningham, Augusta, stated that farmers replanted five times in ant infested fields in his vicinity.
April 23, ’14, W. Russell, Winfield, replanted 80 acres infested with ants three times last year and was finally left with about a twenty acre stand.
Feb. — ’15, Frank Lister, Olpe, says he had 20 acres of kafir destroyed by ants last year.
Jan. — ’16, Henry Hanson, Rosalia, states that the ant is very bad. Last year he replanted seven times without obtaining a stand.
House Pest This phase of the insect’s depredations has not attracted much attention in Kansas. Several reports of yellow ants as pests in houses in this state have, upon investigation, proved to be the larger ant, Monomorium pharaonic. There are but two records in the files of the Experiment Station of S. molesta as a household pest. One is from Kansas City, Mo., and the other a record of the ant being abundant in a clothes closet in Manhattan.
However, there are numerous accounts of the species infesting houses in other localities. Say (loc. cit.) records the ants as being found in houses in great numbers where they eat vegetable food, olive oil, and grease. Fitch (1856, p. 129) calls it the most abundant and annoying ant in the State of New York, where it is common in dwellings, being attracted by sweet-meats, preserves and other sweetish substances. As a pest of insect collections, he says: “I have experienced some difficulty in preserving my collection of insects from this depredator, some box or drawer not perfectly tight being invaded by them ere I am aware of it, almost every season. But by crushing every individual which does not escape into some crevice, and permitting their dead bodies to remain where they are slain, their comrades take warning and cease to frequent the spot. The vapor of camphor also repels them.” Packard (1880, p. 185) states that Myrmica molesta is found in houses all over the world. Evidently, he confused the species with other house ants, for S. molesta is a native North American ant and is not so widely distributed as Packard would lead us to believe. Webster (1890, pp. 257-258) found the ants burrowing into cured hams and ripe apples. Later (1893, p. 158) he states: “Several times this insect has made itself exceedingly disagreeable in my own house, by its presence in the pantry, and while in Washington some years since, the artist of the Division of Pomology, Department of Agriculture, complained to me of the trouble he experienced from a closely allied species, Solenopsis debilis, Mayr, eating the paints with which he was coloring the wax models of fruit.” Wheeler in different articles (1905, pp. 377-378; 1910, p. 427) mentions the species as a pest of houses and disproves Forel’s (1901, pp. 344-345) assertion that S. molesta does not occur in houses. Barber (1912, p. 181), in a paper on the avocado weevil, discussing seeds of the avocado infested with weevil, says: “Unfortunately the seed lay for a time on his desk subject to the attack, of the ant pest (Solenopsis debilis) from which the Bureau of Entomology suffers. . . .” Tanquary (1912, p. 138) reports that the ant is sometimes found in houses. Herrick (1914, p. 178) states “The tiny thief-ant (Solenopsis molesta) is a native ant that occasionally leaves its natural haunts and builds its nest in houses, where the occupants become pests in kitchens and pantries.”
Life History Traits
- Queen number: polygynous (Frumhoff & Ward, 1992)
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- molesta. Myrmica molesta Say, 1836: 293 (q.) U.S.A. Wheeler, G.C. & Wheeler, J. 1955c: 134 (l.); Petralia & Vinson, 1980: 383 (l.); Crozier, 1970: 116 (k.). Combination in Solenopsis: Mayr, 1863: 407; in S. (Diplorhoptrum): Creighton, 1950a: 237. Senior synonym of debilis, exigua, minuta: Emery, 1895c: 277; Emery, 1896g: 85.
- minuta. Myrmica minuta Say, 1836: 294 (w.) U.S.A. Junior synonym of molesta: Emery, 1895c: 277.
- exigua. Myrmica (Tetramorium) exigua Buckley, 1867: 342 (w.q.) U.S.A. Junior synonym of molesta: Emery, 1895c: 277. See also: Wheeler, W.M. 1902f: 28.
- debilis. Solenopsis debilis Mayr, 1886d: 461 (w.q.m.) U.S.A. Junior synonym of molesta: Emery, 1895c: 277; Emery, 1896g: 85.
Pacheco and Mackay (2013) - None known to exist (type locality, Indiana). Apparently, none of the type series exist today. We picked the most common specimens that range near the type locality to anchor the identity of this species. Additionally, we knew the identity of closely related species. Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Pacheco and Mackay (2013) - Measurements (n=6). TL 1.38-1.62 (1.50); HL 0.420-0.510 (0.457); HW 0.360-0.432 (0.386); EL 0.036-0.042 (0.040); ED 0.030-0.036 (0.032); SL 0.282-0.348 (0.317); FSL 0.132-0.156 (0.141); CI 81.1-87.8 (84.5); SI 64.7-72.9 (69.4); PL 0.072-0.096 (0.083); PW 0.120-0.156 (0.126); PI 57.7-80.0 (66.3); PPL 0.102-0.120 (0.108); PPW 0.120-0.162 (0.135); PPI 74.1-85.7 (80.4); WL 0.300-0.342 (0.325); PSL 0.030-0.036 (0.032); PSW 0.030.
Small; concolorous yellow to pale brown; head longer than wide, sides nearly straight, finely punctate; lateral clypeal teeth well developed, extralateral teeth absent; clypeal carinae well defined; scape long, nearly reaching posterior lateral corner of head; minor funicular segments moderately long; eye small, 3-5 ommatidia; pronotum finely punctate, smooth and shiny between punctures; mesopleuron smooth and shiny; notopropodeal suture well depressed, notch-shaped, groove breaks sculpture of mesosoma; posterior border of propodeum rounded; propodeal spiracle small, round; metapleuron horizontally striated; petiole wider than postpetiole viewed laterally; petiolar peduncle with minute angle ventrally; postpetiolar node semicircular viewed laterally, lacking tooth or flange ventrally.
Abundantly hairy, pilosity yellow; erect and suberect hairs covering all body surfaces; scape with numerous appressed hairs; dorsum of mesosoma with hairs of various lengths (0.060-0.120 mm); hairs on petiole, postpetiole and gaster curve posteriorly.
Pacheco and Mackay (2013) - Measurements (n=6). TL 4.68-5.64 (5.36); HL 0.720-0.840 (0.781); HW 0.642-0.780 (0.743); EL 0.240; ED 0.180; MOL 0.072-0.120 (0.103); MOD 0.072-0.120 (0.097); SL 0.516-0.540 (0.536); FSL 0.300; CI 89.2-98.5 (95.1); SI 64.3-71.7 (68.7); PSL 0.072-0.078 (0.075); PSW 0.060; PL 0.120; PW 0.276-0.384 (0.350); PI 31.3-43.5 (34.7); PPL 0.276-0.360 (0.306); PPW 0.330-0.420 (0.405); PPI 71.4-85.7 (75.8); WL 0.960-1.20 (1.12).
Moderately large; concolorous yellow to pale brown; head longer than wide, posterior border slightly concave, semi-coarsely punctate; lateral clypeal teeth well developed, extralateral teeth absent; clypeal carinae well defined; frontal lobes vertically striated; eyes large, extend 0.084 mm past lateral margin of head; scapes long, reach lateral ocelli; medial ocellus small, depigmented; dorsum of mesosoma semi-coarsely punctate, smooth and shiny between punctures; posterior propodeal margin viewed laterally slightly angled; propodeal spiracle small, oval; metapleuron horizontally striated; sides of petiolar and postpetiolar nodes horizontally striated; petiolar peduncle with thin flange ventrally; postpetiole lacking tooth or flange ventrally.
Abundantly hairy, pilosity yellow; numerous erect and suberect hairs of various lengths on all body surfaces; hairs on dorsum of mesosoma long (0.120-0.180 mm); hairs on petiole and postpetiole long (up to 0.240 mm), curve posteriorly.
Pacheco and Mackay (2013) - Measurements (n=6). TL 3.48-4.32 (3.85); HL 0.498-0.516 (0.504); HW 0.510-0.534 (0.518); EL 0.276-0.300 (0.282); ED 0.216-0.228 (0.225); MOL 0.078-0.108 (0.091); MOD 0.102-0.120 (0.111); SL 0.204-0.228 (0.212); FSL 0.960-1.02 (0.972); CI 102-104 (103); SI 40.7-44.7 (42.3); PSL 0.078-0.090 (0.083); PSW 0.060; PL 0.132-0.144 (0.138); PW 0.252-0.282 (0.266); PI 48.9-55.8 (52.1); PPL 0.240; PPW 0.300-0.360 (0.324); PPI 66.7-80.0 (74.4); WL 0.960-1.08 (1.05).
Moderately large; concolorous dark brown to bicolored (darker head and gaster than mesosoma); head smooth and shiny with scattered fine punctures, wider than long; anterior clypeal margin convex, lacking teeth or carinae; frontal lobes vertically striated, extend laterally then anteriorly to clypeal margin; antennae long, yellow; eyes large, extend 0.120 mm past lateral margin of head; medial ocellus large, lacking pigment; semi-coarse punctures on pronotum, smooth and shiny between punctures; posterior propodeal margin viewed laterally rounded; propodeal spiracle small, round; propodeum striated; petiolar node rounded dorsally, horizontally striated, peduncle lacking tooth or flange ventrally, but with angle; postpetiolar node flattened dorsally, horizontally striated, lacking tooth or flange ventrally.
Abundantly hairy, pilosity yellow; erect and suberect hairs of various lengths covering all body surfaces; most hairs on pronotum about 0.120 mm in total length; hairs on petiole and postpetiole curve posteriorly.
- n = 11, 2n = 22 (USA) (Crozier, 1970b).
- Baker, A.J., Heraty, J.M., Mottern, J., Hang, J.Z., Hines, H.M., Lemmon, A.R., Lemmon, E.M. 2019. Inverse dispersal patterns in a group of ant parasitoids (Hymenoptera: Eucharitidae: Oraseminae) and their ant hosts. Systematic Entomology 45: 1–19 (doi:10.1111/syen.12371).
- Creighton, W. S. 1950a. The ants of North America. Bull. Mus. Comp. Zool. 104: 1-585 (page 237, Combination in S. (Diplorhoptrum))
- Crozier, R. H. 1970a. Karyotypes of twenty-one ant species (Hymenoptera: Formicidae), with reviews of the known ant karyotypes. Can. J. Genet. Cytol. 12: 109-128 (page 116, karyotype described)
- Emery, C. 1895d. Beiträge zur Kenntniss der nordamerikanischen Ameisenfauna. (Schluss). Zool. Jahrb. Abt. Syst. Geogr. Biol. Tiere 8: 257-360 (page 277, Senior synonym of debilis, exigua and minuta)
- Emery, C. 1896g. Studi sulle formiche della fauna neotropica. XVII-XXV. Bull. Soc. Entomol. Ital. 28: 33-107 (page 85, Senior synonym of debilis, exigua and minuta)
- Hayes, W. P. 1920. Solenopsis molesta Say (Hym.): a biological study. Kansas State Agricultural College, Agricultural Experiment Station. Manhattan, KS. Technical bulletin No. 7. 55 p.
- Mackay, W. P. and E. Mackay. 2002. The ants of New Mexico (Hymenoptera: Formicidae). Edwin Mellen Press, Lewiston, NY.
- Mayr, G. 1863a. Formicidarum index synonymicus. Verh. K-K. Zool.-Bot. Ges. Wien 13: 385-460 (page 407, Combination in Solenoopsis)
- Pacheco, J.A. & Mackay, W.P. 2013. The systematics and biology of the New World thief ants of the genus Solenopsis (Hymenoptera: Formicidae). Edwin Mellen Press, Lewiston, New York. 501 pp.
- Petralia, R. S.; Vinson, S. B. 1980 . Comparative anatomy of the ventral region of ant larvae, and its relation to feeding behavior. Psyche (Camb.) 86: 375-394 (page 383, larva described)
- Polidori, C., Rodriguez-Flores, P.C., Garcia-Paris, M. 2020. Ants as prey for the endemic and endangered Spanish tiger beetle Cephalota dulcinea (Coleoptera: Carabidae). Annales de la Société entomologique de France (N.S.) (doi:10.1080/00379271.2020.1791252).
- Say, T. 1836. Descriptions of new species of North American Hymenoptera, and observations on some already described. Boston J. Nat. Hist. 1: 209-305 (page 293, queen described)
- Sharaf, M.R., Gotzek, D., Guénard, B., Fisher, B.L., Aldawood, A.S., Al Dhafer, H.M., Mohamed, A.A. 2020. Molecular phylogenetic analysis and morphological reassessments of thief ants identify a new potential case of biological invasions. Scientific Reports 10, 12040 (doi:10.1038/s41598-020-69029-4).
- Wheeler, G. C.; Wheeler, J. 1955c. The ant larvae of the myrmicine tribe Solenopsidini. Am. Midl. Nat. 54: 119-141 (page 134, larva described)
References based on Global Ant Biodiversity Informatics
- Adams T. A., W. J. Staubus, and W. M. Meyer. 2018. Fire impacts on ant assemblages in California sage scrub. Southwestern Entomologist 43(2): 323-334.
- 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.
- Amstutz M. E. 1943. The ants of the Kildeer plain area of Ohio (Hymenoptera, Formicidae). The Ohio Journal of Science 43(4): 165-173.
- Backlin, Adam R., Sara L. Compton, Zsolt B. Kahancza and Robert N. Fisher. 2005. Baseline Biodiversity Survey for Santa Catalina Island. Catalina Island Conservancy. 1-45.
- Banschbach V. S., and E. Ogilvy. 2014. Long-term Impacts of Controlled Burns on the Ant Community (Hymenoptera: Formicidae) of a Sandplain Forest in Vermont. Northeastern Naturalist 21(1): 1-12.
- Beckmann R. L., and J. M. Stucky. 1981. Extrafloral Nectaries and Plant Guarding in Ipomoea pandurata (L.) G. F. W. Mey. (Convolvulaceae). American Journal of Botany 68(1): 72-79.
- Belcher A. K., M. R. Berenbaum, and A. V. Suarez. 2016. Urbana House Ants 2.0.: revisiting M. R. Smith's 1926 survey of house-infesting ants in central Illinois after 87 years. American Entomologist 62(3): 182-193.
- Bestelmeyer B. T., and J. A. Wiens. 2001. Local and regional-scale responses of ant diversity to a semiarid biome transition. Ecography 24: 381-392.
- Blacker, N.C. 1992. Some Ants from Southern Vancouver Island, British Columbia. J. Entomol. Soc. Bri. Columbia 89:3-12.
- Blacker, N.C. 1992. Some ants (Hymenoptera: Formicidae) from Southern Vancouver Island, British Columbia. Journal of the Entomological Society of British Columbia 89:3-12
- Boulton A. M., Davies K. F. and Ward P. S. 2005. Species richness, abundance, and composition of ground-dwelling ants in northern California grasslands: role of plants, soil, and grazing. Environmental Entomology 34: 96-104
- Boulton A.M. and P.S. Ward. 2002. Ants. Chapter 5 in A New island Biogeography of the Sea of Cortes. T.J. Case, M.L. Cody and E. Ezcurra. Oxford university Press.
- Braman C. A., and B. T. Forschler. 2018. Survey of Formicidae attracted to protein baits on Georgia’s Barrier Island dunes. Southeastern Naturalist 17(4): 645-653.
- Buren W. F. 1944. A list of Iowa ants. Iowa State College Journal of Science 18:277-312
- Callcott A. M. A., D. H. oi, H. L. Collins, D. F. Williams, and T. C. Lockley. 2000. Seasonal Studies of an Isolated Red Imported Fire Ant (Hymenoptera: Formicidae) Population in Eastern Tennessee. Environmental Entomology, 29(4): 788-794.
- Campbell K. U., and T. O. Crist. 2017. Ant species assembly in constructed grasslands isstructured at patch and landscape levels. Insect Conservation and Diversity doi: 10.1111/icad.12215
- Canadensys Database. Dowloaded on 5th February 2014 at http://www.canadensys.net/
- Cancino, E.R., D.R. Kasparan, J.M.A. Coronado Blanco, S.N. Myartseva, V.A. Trjapitzin, S.G. Hernandez Aguilar and J. Garcia Jimenez. 2010. Himenópteros de la Reserva El Cielo, Tamaulipas, México. Dugesiana 17(1):53-71
- 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.
- Clark Adam. Personal communication on November 25th 2013.
- Clarke K.M., Fisher B.L. and LeBuhn G. 2008. The influece of urban park characteristics on ant (Hymenoptera, Formicidae) communities. Urban Ecosyst 11: 317-334
- Cole A. C., Jr. 1942. The ants of Utah. American Midland Naturalist 28: 358-388.
- Cole A. C., Jr. 1949. The ants of Mountain Lake, Virginia. Journal of the Tennessee Academy of Science 24: 155-156.
- Coovert G. A. 2005. The Ants of Ohio (Hymenoptera: Formicidae). Ohio Biological Survey, Inc. 15(2): 1-207.
- Coovert, G.A. 2005. The Ants of Ohio (Hymenoptera: Formicidae) Ohio Biological Survey Bulletin New Series Volume 15(2):1-196
- Crozier R. H. 1970. Karyotypes of twenty-one ant species (Hymenoptera: Formicidae), with reviews of the known ant karyotypes. Can. J. Genet. Cytol. 12: 109-128.
- Dash S. T. and L. M. Hooper-Bui. 2008. Species diversity of ants (Hymenoptera: Formicidae) in Louisiana. Conservation Biology and Biodiversity. 101: 1056-1066
- 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., K. Towle, D. N. Morrison, and S. L. Pelini. 2013. Community Structure, Ecological and Behavioral Traits of Ants (Hymenoptera: Formicidae) in Massachusetts Open and Forested Habitats. Northeastern Naturalist 20: 1-12.
- Del Toro, I. 2010. PERSONAL COMMUNICATION. MUSEUM RECORDS COLLATED BY ISRAEL DEL TORO
- Dennis C. A. 1938. The distribution of ant species in Tennessee with reference to ecological factors. Annals of the Entomological Society of America 31: 267-308.
- Des Lauriers J., and D. Ikeda. 2017. The ants (Hymenoptera: Formicidae) of the San Gabriel Mountains of Southern California, USA with an annotated list. In: Reynolds R. E. (Ed.) Desert Studies Symposium. California State University Desert Studies Consortium, 342 pp. Pages 264-277.
- DuBois M. B. 1981. New records of ants in Kansas, III. State Biological Survey of Kansas. Technical Publications 10: 32-44
- DuBois M. B. 1985. Distribution of ants in Kansas: subfamilies Ponerinae, Ecitoninae, and Myrmicinae (Hymenoptera: Formicidae). Sociobiology 11: 153-1335
- 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
- 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.
- Fernandes, P.R. XXXX. Los hormigas del suelo en Mexico: Diversidad, distribucion e importancia (Hymenoptera: Formicidae).
- Fisher B. L. 1997. A comparison of ant assemblages (Hymenoptera, Formicidae) on serpentine and non-serpentine soils in northern California. Insectes Sociaux 44: 23-33
- Forster J.A. 2005. The Ants (hymenoptera: Formicidae) of Alabama. Master of Science, Auburn University. 242 pages.
- Frye J. A., T. Frye, and T. W. Suman. 2014. The ant fauna of inland sand dune communities in Worcester County, Maryland. Northeastern Naturalist, 21(3): 446-471.
- Gans M. J., J. R. Arnold, A. Cohuo, L. Castro, D. Lam, and C. Wiley. 2016. Survey of ant species in Rockwall County, Texas. Southwestern Entomologist 41(2): 373-378.
- General D. M., and L. C. Thompson. 2011. New Distributional Records of Ants in Arkansas for 2009 and 2010 with Comments on Previous Records. Journal of the Arkansas Academy of Science 65: 166-168.
- General D., and L. Thompson. 2008. Ants of Arkansas Post National Memorial: How and Where Collected. Journal of the Arkansas Academy of Science 62: 52-60.
- General D., and L. Thompson. 2008. New distributional records of ants in Arkansas. Journal of the Arkansas Academy of Science 62: 148-150.
- General D.M. & Thompson L.C. 2007. Ants (Hymenoptera: Formicidae) of Arkansas Post National Memorial. Journal of the Arkansas Acaedemy of Science. 61: 59-64
- General D.M. & Thompson L.C. 2008. New Distributional Records of Ants in Arkansas for 2008. Journal of the Arkansas Academy of Science. 63: 182-184
- Gibbs M. M., P. L. Lambdin, J. F. Grant, and A. M. Saxton. 2003. Ground-inhabiting ants collected in a mixed hardwood southern Appalachian forest in Eastern Tennessee. Journal of the Tennessee Academy of Science 78(2): 45-49.
- Greenberg L., M. Martinez, A. Tilzer, K. Nelson, S. Koening, and R. Cummings. 2015. Comparison of different protocols for control of the Red Imported Fire Ant, Solenopsis invicta Buren (Hymenoptera: Formicidae), in Orange County, California, including a list of co-occurring ants. Southwestern Entomologist 40(2): 297-305.
- Gregg, R.T. 1963. The Ants of Colorado.
- Guénard B., K. A. Mccaffrey, A. Lucky, and R. R. Dunn. 2012. Ants of North Carolina: an updated list (Hymenoptera: Formicidae). Zootaxa 3552: 1-36.
- Headley A. E. 1943. The ants of Ashtabula County, Ohio (Hymenoptera, Formicidae). The Ohio Journal of Science 43(1): 22-31.
- Heithaus R. E., and M. Humes. 2003. Variation in Communities of Seed-Dispersing Ants in Habitats with Different Disturbance in Knox County, Ohio. OHIO J. SCI. 103 (4): 89-97.
- Hess C. G. 1958. The ants of Dallas County, Texas, and their nesting sites; with particular reference to soil texture as an ecological factor. Field and Laboratory 26: 3-72.
- 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
- Hill, J.G. 2006. Ants collected at Okatibbee Lake, Lauderdale County, Mississippi
- Hoey-Chamberlain R. V., L. D. Hansen, J. H. Klotz and C. McNeeley. 2010. A survey of the ants of Washington and Surrounding areas in Idaho and Oregon focusing on disturbed sites (Hymenoptera: Formicidae). Sociobiology. 56: 195-207
- Holway D.A. 1998. Effect of Argentine ant invasions on ground-dwelling arthropods in northern California riparian woodlands. Oecologia. 116: 252-258
- Ipser R. M. 2004. Native and exotic ants (Hymenoptera: Formicidae) of Georgia: Ecological Relationships with implications for development of biologically-based management strategies. Doctor of Philosophy thesis, University of Georgia. 165 pages.
- Ivanov K. 2019. The ants of Ohio (Hymenoptera, Formicidae): an updated checklist. Journal of Hymenoptera Research 70: 65–87.
- Ivanov K., L. Hightower, S. T. Dash, and J. B. Keiper. 2019. 150 years in the making: first comprehensive list of the ants (Hymenoptera: Formicidae) of Virginia, USA. Zootaxa 4554 (2): 532–560.
- Johnson R. Personnal Database. Accessed on February 5th 2014 at http://www.asu.edu/clas/sirgtools/resources.htm
- Johnson, R.A. and P.S. Ward. 2002. Biogeography and endemism of ants (Hymenoptera: Formicidae) in Baja California, Mexico: a first overview. Journal of Biogeography 29:10091026/
- Jusino-Atresino R., and S. A. Phillips, Jr. 1992. New ant records for Taylor Co., Texas. The Southern Naturalist 34(4): 430-433.
- Kittelson P. M., M. P. Priebe, and P. J. Graeve. 2008. Ant Diversity in Two Southern Minnesota Tallgrass Prairie Restoration Sites. Jour. Iowa Acad. Sci. 115(14): 2832.
- Kjar D., and Z. Park. 2016. Increased ant (Hymenoptera: Formicidae) incidence and richness are associated with alien plant cover in a small mid-Atlantic riparian forest. Myrmecological News 22: 109-117.
- Knowlton G. F. 1970. Ants of Curlew Valley. Proceedings of the Utah Academy of Sciences, Arts and Letters 47(1): 208-212.
- La Rivers I. 1968. A first listing of the ants of Nevada. Biological Society of Nevada, Occasional Papers 17: 1-12.
- Longino J. T., and D. B. Booher. 2019. Expect the unexpected: a new ant from a backyard in Utah. Western North American Naturalist 79(4): 496–499.
- Lopez R., and D. A. Potter. 2003. Biodiversity of ants (Hymenoptera: Formicidae) in golf course and lawn turf habitats in Kentucky. Sociobiology 42(3): 701-713.
- Lynch J. F. 1981. Seasonal, successional, and vertical segregation in a Maryland ant community. Oikos 37: 183-198.
- 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., J. G. Hill, and R. L. Brown. 2010. Native and exotic ant in Mississippi state parks. Proceedings: Imported Fire Ant Conference, Charleston, South Carolina, March 24-26, 2008: 74-80.
- MacGown, J.A and J.A. Forster. 2005. A preliminary list of the ants (Hymenoptera: Formicidae) of Alabama, U.S.A. Entomological News 116(2):61-74
- MacGown, J.A. and JV.G. Hill. Ants of the Great Smoky Mountains National Park (Tennessee and North Carolina).
- MacGown, J.A. and R.L. Brown. 2006. Observations on the High Diversity of Native Ant Species Coexisting with Imported Fire Ants at a Microspatial Scale in Mississippi. Southeastern Naturalist 5(4):573-586
- 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.
- Mackay, W.P. and E. Mackay. XXXX. The Ants of New Mexico
- Mann H. R., E. Rowe, J. Selfridge, and D. L. Price. 2018. Leaf litter and arboreal ants (Hymenoptera: Formicidae) in a Mid-Atlantic Forest. Northeastern Naturalist 25(2): 341-354.
- Martelli, M.G., M.M. Ward and Ann M. Fraser. 2004. Ant Diversity Sampling on the Southern Cumberland Plateau: A Comparison of Litter Sifting and Pitfall Trapping. Southeastern Naturalist 3(1): 113-126
- Matsuda T., G. Turschak, C. Brehme, C. Rochester, M. Mitrovich, and R. Fisher. 2011. Effects of Large-Scale Wildfires on Ground Foraging Ants (Hymenoptera: Formicidae) in Southern California. Environmental Entomology 40(2): 204-216.
- McDonald D. L., D. R. Hoffpauir, and J. L. Cook. 2016. Survey yields seven new Texas county records and documents further spread of Red Imported Fire Ant, Solenopsis invicta Buren. Southwestern Entomologist, 41(4): 913-920.
- Menke S. B., E. Gaulke, A. Hamel, and N. Vachter. 2015. The effects of restoration age and prescribed burns on grassland ant community structure. Environmental Entomology http://dx.doi.org/10.1093/ee/nvv110
- Menke S. B., and N. Vachter. 2014. A comparison of the effectiveness of pitfall traps and winkler litter samples for characterization of terrestrial ant (Formicidae) communities in temperate savannas. The Great Lakes Entomologist 47(3-4): 149-165.
- Menozzi C. 1932. Formiche del Nord America raccolte dal Prof. F. Silvestri. Bollettino del Laboratorio di Zoologia Generale e Agraria della Reale Scuola Superiore d'Agricoltura. Portici. 26: 310-312.
- 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.
- MontBlanc E. M., J. C. Chambers, and P. F. Brussard. 2007. Variation in ant populations with elevation, tree cover, and fire in a Pinyon-Juniper-dominated watershed. Western North American Naturalist 67(4): 469491.
- Moody J. V., and O. F. Francke. 1982. The Ants (Hymenoptera, Formicidae) of Western Texas Part 1: Subfamily Myrmicinae. Graduate Studies Texas Tech University 27: 80 pp.
- Munsee J. R. 1968. Nine species of ants (Formicidae) recently recorded from Indiana. Proc. Indiana Acad. Sci. 77: 222-227.
- Nuhn, T.P. and C.G. Wright. 1979. An Ecological Survey of Ants (Hymenoptera: Formicidae) in a Landscaped Suburban Habitat. American Midland Naturalist 102(2):353-362
- 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.
- Ostoja S. M., E. W. Schupp, and K. Sivy. 2009. Ant assemblages in intact big sagebrush and converted cheatgrass-dominates habitats in Tooele County, Utah. Western North American Naturalist 69(2): 223234.
- Pacheco J. A., and W. P. Mackay. 2013. The systematics and biology of the New World thief ants of the genus Solenopsis (Hymenoptera: Formicidae). Lewiston, New York: Edwin Mellen Press, 501 pp.
- Parson G. L., G Cassis, A. R. Moldenke, J. D. Lattin, N. H. Anderson, J. C. Miller, P. Hammond, T. Schowalter. 1991. Invertebrates of the H.J. Andrews Experimental Forest, western Cascade Range, Oregon. V: An annotated list of insects and other arthropods. Gen. Tech. Rep. PNW-GTR-290. Portland, OR: U.S. Department of Agriculture, Forest Service, Pacific Northwest Research Station. 168 p.
- Pennsylvania Department of Agriculture Collection (Pers. Comm. Sven-Erik Spichiger 23 Dec 2017)
- Ratchford, J.S., S.E. Wittman, E.S. Jules, A.M. Ellison, N.J. Gotelli and N.J. Sanders. 2005. The effects of fire, local environment and time on ant assemblages in fens and forests. Diversity and Distributions 11:487-497.
- 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.
- Ruhren, S. 2003. Seed Predators Are Undeterred by Nectar-Feeding Ants on Chamaecrista nictitans (Caesalpineaceae). Plant Ecology 166(2):189-198
- Sanders, N.J. 2004.Immediate Effects of Fire on the Invasive Argentine Ant, Linepithema humile. The Southwestern Naturalist 49(2) :246-250
- Shik, J., A. Francoeur and C. Buddle. 2005. The effect of human activity on ant species (Hymenoptera: Formicidae) richness at the Mont St. Hilaire Biosphere Reserve, Quebec. Canadian Field-Naturalist 119(1): 38-42.
- Smith F. 1861. Catalogue of hymenopterous insects collected by Mr. A. R. Wallace in the islands of Ceram, Celebes, Ternate, and Gilolo. [part]. Journal and Proceedings of the Linnean Society of London. Zoology 6: 36-48.
- Smith M. R. 1935. A list of the ants of Oklahoma (Hymen.: Formicidae). Entomological News 46: 235-241.
- Smith M. R. 1952. On the collection of ants made by Titus Ulke in the Black Hills of South Dakota in the early nineties. Journal of the New York Entomological Society 60: 55-63.
- Smith M. R., and W. A. Morrison. 1916. South Carolina ants. Entomological News 27: 110-111.
- Staubus W. J., E. S. Boyd, T. A. Adams, D. M. Spear, M. M. Dipman, W. M. Meyer III. 2015. Ant communities in native sage scrub, non-native grassland, and suburban habitats in Los Angeles County, USA: conservation implications. Journal of Insect Conservervation 19:669–680
- 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.
- Toennisson T. A., N. J. Sanders, W. E. Klingeman, and K. M. Vail. 2011. Influences on the Structure of Suburban Ant (Hymenoptera: Formicidae) Communities and the Abundance of Tapinoma sessile. Environ. Entomol. 40(6): 1397-1404.
- Uno S., J. Cotton, and S. M. Philpott. Diversity, abundance, and species composition of ants in urban green spaces. Urban Ecosyst 13: 425441.
- Van Pelt A. F. 1956. The ecology of the ants of the Welaka Reserve, Florida (Hymenoptera: Formicidae). American Midland Naturalist 56: 358-387
- Van Pelt A. F. 1958. The ecology of the ants of the Welaka Reserve, Florida (Hymenoptera: Formicidae). Part II. Annotated list. American Midland Naturalist 59: 1-57
- Van Pelt A. F. 1966. Activity and density of old-field ants of the Savannah River Plant, South Carolina. Journal of the Elisha Mitchell Scientific Society 82: 35-43.
- Van Pelt A., and J. B. Gentry. 1985. The ants (Hymenoptera: Formicidae) of the Savannah River Plant, South Carolina. Dept. Energy, Savannah River Ecology Lab., Aiken, SC., Report SRO-NERP-14, 56 p.
- Van Pelt, A. 1983. Ants of the Chisos Mountains, Texas (Hymenoptera: Formicidae) . Southwestern Naturalist 28:137-142.
- 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
- Ward P. S. 1987. Distribution of the introduced Argentine ant (Iridomyrmex humilis) in natural habitats of the lower Sacramento Valley and its effects on the indigenous ant fauna. Hilgardia 55: 1-16
- Ward P.S. and A.M. Boulton. 2002. Checklist of the ants of the Gulf of California Islands. In Island Biogeography of the sea of Cortes. T.J. Case, M.L. Cody and E. Ezcurra Editors. 690 pp.
- Warren, L.O. and E.P. Rouse. 1969. The Ants of Arkansas. Bulletin of the Agricultural Experiment Station 742:1-67
- Wetterer, J. K.; Ward, P. S.; Wetterer, A. L.; Longino, J. T.; Trager, J. C.; Miller, S. E. 2000. Ants (Hymenoptera: Formicidae) of Santa Cruz Island, California. Bulletin of the Southern California Academy of Sciences 99:25-31.
- Wetterer, J.K., P.S. Ward, A.L. Wetterer, J.T. Longino, J.C. Trager and S.E. Miller. 2000. Ants (Hymenoptera:Formicidae) of Santa Cruz Island, California. Bulletin of the Southern California Academy of Science 99(1):25-31.
- Wheeler G. C. and Wheeler J. 1973. Ants of Deep Canyon. Riverside, Calif.: University of California, xiii + 162 pp
- 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. 1901. Notices biologiques sur les fourmis Mexicaines. Annales de la Société Entomologique de Belgique. 45: 199-205.
- Wheeler W. M. 1901. The compound and mixed nests of American ants. Part II. The known cases of social symbiosis among American ants. American Naturalist. 35: 513-539.
- Wheeler W. M. 1905. An annotated list of the ants of New Jersey. Bulletin of the American Museum of Natural History. 21: 371-403.
- 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, G.C. and J. Wheeler. 1985. A checklist of Texas ants. Prairie Naturalist 17:49-64.
- 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
- Yap H. H., and C. Y. Lee. 1994. A preliminary study on the species composition of household ants on Penang island, Malaysia. Journal of Bioscience 5(1-2): 64-66.
- 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
- Zettler J. A., M. D. Taylor, C. R. Allen, and T. P. Spira. 2004. Consequences of Forest Clear-Cuts for Native and Nonindigenous Ants (Hymenoptera: Formicidae). Ann. Entomol. Soc. Am. 97(3): 513-518.