Camponotus novaeboracensis
Camponotus novaeboracensis | |
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Scientific classification | |
Kingdom: | Animalia |
Phylum: | Arthropoda |
Class: | Insecta |
Order: | Hymenoptera |
Family: | Formicidae |
Subfamily: | Formicinae |
Tribe: | Camponotini |
Genus: | Camponotus |
Subgenus: | Camponotus |
Species complex: | herculeanus |
Species: | C. novaeboracensis |
Binomial name | |
Camponotus novaeboracensis (Fitch, 1855) | |
Synonyms | |
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Camponotus novaeboracensis nests in rotten wood, (Mackay and Mackay, 2002), in and under logs and stumps, in dead branches on the ground and under bark, boards, or even under stones (especially incipient nests) and cow dung (Wheeler and Wheeler, 1963; Hansen and Klotz 2005). New nests can be found in hollow twigs. Colonies are small, with about 3000 workers (Hansen and Klotz 2005). Gibson (1989) discusses the production of soldiers during colony growth, with older colonies having a higher proportion of majors. Brood and sexuals were found in nests in June, August and September. Dealate females were collected in April, June, July and August, a flight was observed in June (21:00 - 22:00). (Mackay, 2019)
Photo Gallery
Identification
The following information is derived from Mackay, New World Carpenter Ants (2019)
Compare with Camponotus chromaiodes, Camponotus herculeanus, Camponotus pennsylvanicus.
The majors, minors and females of C. novaeboracensis have a black head and gaster and a red mesosoma, making them large very attractive ants. The females can be completely black. Erect and suberect setae are sparse on the head, mesosoma, petiole and gaster and absent on the cheeks, malar area, sides of the head, posterior lateral corners and tibiae, except for 2 rows of setae on the flexor surface.
The males are moderately large (total length 8 mm) black ants.
Comparisons
The major of C. novaeboracensis has lateral clypeal angles, which are not well developed. The antennal scapes are without erect and suberect setae (except at the apex) and extend nearly 1 funicular segment past the posterior lateral corners of the head in both the majors and the females. The pubescence on the gaster of all castes of C. novaeboracensis is very fine, with none of the setae overlapping adjacent setae. The punctures on the head are of two sizes, the majority are very fine, and the other scattered punctures are larger in diameter. These characteristics usually separate this species from others of the subgenus Camponotus.
Camponotus novaeboracensis is very similar to Camponotus pennsylvanicus (S Canada, US). They can be separated as the workers and often the females of C. novaeboracensis are bicolored, whereas they are nearly always concolorous black in C. pennsylvanicus. Questionable specimens can be separated as the setae on the gaster of workers and females of C. novaeboracensis are relatively short, with few or no appressed setae overlapping adjacent setae, whereas in C. pennsylvanicus the setae are longer and most overlap adjacent setae. Unfortunately, neither of these characteristics serve to separate the males, and there are no obvious characters which will separate them. Camponotus novaeboracensis is sympatric with C. pennsylvanicus in Iowa with no integration which is strong evidence that they are separate species (Buren, 1944).
Camponotus novaeboracensis can be confused with Camponotus herculeanus (S Canada, US), and the two species are genetically similar (Sämi Schär, et al., 2018). The major workers are usually easy to separate, as the scapes of C. herculeanus do not extend past the posterior lateral corner of the head (they extend well past the corners in C. novaeboracensis). The minor workers of C. novaeboracensis can often be separated as the mesosoma of C. herculeanus is mostly black, or dark red, whereas it is normally red, contrasting with the black head and gaster in C. novaeboracensis. The females of the two species are very difficult to separate. The female of C. herculeanus has a wider head, with the cephalic index ranging from 113 - 114. The cephalic index of C. novaeboracensis ranges from 106 to 108. The dorsum of the mesosoma of the female of C. herculeanus is nearly always black, whereas it is normally partially red in C. novaeboracensis.
It is possible to confuse C. novaeboracensis with Camponotus chromaiodes as they are both mostly dark, with a partially red mesosoma. They can be best separated as the setae on the dorsum of the gaster of C. novaeboracensis are short and similar to the color of the background, whereas they are longer and golden on the gaster of C. chromaiodes, including on the major, minor and female.
Distribution
The following information is derived from Mackay, New World Carpenter Ants (2019)
Camponotus novaeboracensis is found in several habitats including deciduous forest, pine/oaks on sand, beach maple, hardwood forest, mixed hardwood conifer forest and oak-evergreen forest, as well as oak, ash, cottonwoods, aspen, willow woods and grasslands (Wheeler and Wheeler, 1963) in addition to black cherry forests (Yitbarek et al., 2011), grasslands and shrublands (Barber, 2015) and open fields (Oberg, 2012). Buren (1944) concluded it was more boreal than C. pennsylvanicus.
Latitudinal Distribution Pattern
Latitudinal Range: 62.41323333° to 1.311674476°.
North Temperate |
North Subtropical |
Tropical | South Subtropical |
South Temperate |
- Source: AntMaps
Distribution based on Regional Taxon Lists
Nearctic Region: Canada, United States (type locality).
Distribution based on AntMaps
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. |
Biology
The following information is derived from Mackay, New World Carpenter Ants (2019)
Sanders (1972) studied foraging in C. novaeboracensis and found that the start of seasonal activity was temperature dependent and peaked in mid-summer. Workers forage throughout the day and night.
Food sources include honeydew produced by the membracid, Vanduzea arquata (Say), the sap exudate flowing from a wound in the trunk of a common lilac, Syringa vulgaris, and the carcasses of dead insects (Gotwald, 1968). The behavior of the worker ants in exploiting each of these sources is discussed in detail by Gotwald (1968). It is a honeydew feeder (Oberg, 2012), which tends aphids (Jones, 1929), as well as membracids patrolling bracken fern (Pteridium aquilinum) during the sensitive crozier growth stage. At times these ants remove herbivorous insects from rapidly expanding fronds (Oldenkamp and Douglas, 2011).
Camponotus novaeboracensis is a behaviorally dominant ant (Oberg, 2012) with a strong negative association with the congener Camponotus pennsylvanicus (Thompson and McLachlan, 2007), although it can be a neutrally interacting species found mainly in forest plots (Del Toro et al., 2013).
Camponotus novaeboracensis is the host of the ant cricket Myrmecophilus pergandei (Hebard, 1920), and the principal host for Nemadus triangulum (Coleoptera: Leiodidae) (Peck and Cook, 2007). Reemer (2012) discusses parasitism by the syrphid fly Microdon sp. It is the host of parasites Microdon cothurnatus and M. tristis (Duffield, 1981). The pupae are parasitized by Pseudochalcura gibbosa (Eucharitidae) wasps (Wheeler, 1907; Lachaud, J.-P. and G. Pérez-Lachaud. 2012). Ants carry wasp larvae to the nest and feed them, where the small wasp eats ants (Ellison et al., 2012).
They are the host of the endosymbiotic bacterium Candidatus Blochmannia (Degnan et al., 2004) and the host of Wolbachia bacteria (Wernegreen et al., 2009). They have gram-negative prokaryotic endosymbionts in the follicle cells (Peloquin et al., 2001).
It is an occasional house pest (Mackay and Mackay, 2002; Hansen and Klotz 2005).
Fitzpatrick et al. (2013) used the models MaxEnt and MaxLike to predict the distribution.
It was introduced into Bermuda (Hilburn et al., 1990), but is apparently not established (Wetter and Wetter, 2004).
Additional Notes
The pupae of this medium-sized carpenter ant are often parasitized by small Pseudochalcura gibbosa wasps; the larvae of these wasps are taken back to the nest by the ants as a food source for the developing brood. But the eaten become the eaters, as some of the wasp larvae develop and then devour the ants. (Ellison et al. 2012)
Flight Period
X | X | X | X | ||||||||
Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec |
Source: antkeeping.info. Notes: Washington (May).
- Check details at Worldwide Ant Nuptial Flights Data, AntNupTracker and AntKeeping.
- Explore: Show all Flight Month data or Search these data. See also a list of all data tables or learn how data is managed.
Association with Other Organisms
- Explore: Show all Associate data or Search these data. See also a list of all data tables or learn how data is managed.
- This species is a mutualist for the aphid Chaitophorus nigrae (a trophobiont) (Jones, 1927; Saddiqui et al., 2019).
- This species is a mutualist for the aphid Cinara schwarzii (a trophobiont) (Jones, 1927; Saddiqui et al., 2019).
- This species is a mutualist for the aphid Lachnus solitarius (a trophobiont) (Jones, 1927; Saddiqui et al., 2019).
- This species is a host for the eucharitid wasp Pseudochalcura gibbosa (a parasite) (Universal Chalcidoidea Database) (primary host).
- This species is a host for the cricket Myrmecophilus pergandei (a myrmecophile) in United States.
- This species is a host for the Microdon fly Microdon albicomatus (a predator) (Paulson & Akre, 1991; www.diapriid.org).
- This species is a prey for the Microdon fly Microdon cothurnatus (a predator) (Quevillon, 2018).
- This species is a prey for the Microdon fly Microdon tristis (a predator) (Quevillon, 2018).
- This species is a host for the phorid fly Trucidophora camponoti (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission outside nest).
Life History Traits
- Queen number: monogynous (Frumhoff & Ward, 1992)
Castes
Worker
Images from AntWeb
Worker. Specimen code casent0103349. Photographer April Nobile, uploaded by California Academy of Sciences. | Owned by USNM, Washington, DC, USA. |
Male
Images from AntWeb
Male (alate). Specimen code casent0103350. 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.
- novaeboracensis. Formica novaeboracensis Fitch, 1855: 766 (w.) U.S.A. (New York).
- Type-material: syntype workers (number not stated).
- Type-locality: U.S.A.: New York (A. Fitch).
- Type-depository: unknown (no material known to exist (Creighton, 1950a: 369)).
- [Notes (i): Fitch, 1855: 705, says that his insect specimens will be deposited in the “Entomological department of the Museum of the {N.Y. State Agricultural} Society”, the present whereabouts of which are apparently unknown; (ii) Wheeler, W.M. 1917c: 26 (in text), claimed that Fitch type-material was detected in USNM.]
- [Misspelled as noveboracensis by Wheeler, W.M. 1910d: 340, Creighton, 1950a: 369, Mackay, 2019: 277, and many others.]
- Wheeler, W.M. 1910d: 340 (s.w.q.m.); Wheeler, G.C. & Wheeler, J. 1953e: 182 (l.).
- Combination in Camponotus: Roger, 1863b: 6;
- combination in C. (Camponotus): Emery, 1925b: 72.
- As unavailable (infrasubspecific) name: Wheeler, W.M. 1900c: 47; Wheeler, W.M. 1906b: 23; Wheeler, W.M. 1908f: 625; Wheeler, W.M. 1910d: 340; Wheeler, W.M. 1910g: 571; Wheeler, W.M. 1916m: 601; Wheeler, W.M. 1917a: 557; Wheeler, W.M. 1917c: 27; Wheeler, W.M. 1917i: 466; Cole, 1936a: 39; Wing, 1939: 163; Wesson, L.G. & Wesson, R.G. 1940: 103; Cole, 1942: 388; Smith, M.R. 1951a: 839.
- Junior synonym of herculeanus: Mayr, 1863: 399; Forel, 1874: 96 (in list); Emery & Forel, 1879: 447; Emery & Forel, 1879: 447.
- Junior synonym of pennsylvanicus: Mayr, 1886d: 420; Dalla Torre, 1893: 247; Emery, 1896d: 372 (in list).
- Subspecies of ligniperda: Forel, 1899c: 130.
- Subspecies of herculeanus: Emery, 1925b: 72; Buren, 1944a: 293; Wheeler, G.C. & Wheeler, E.W. 1944: 250; Buren, 1944a: 293.
- Status as species: Roger, 1863b: 6; Creighton, 1950a: 369; Smith, M.R. 1958c: 142; Smith, M.R. 1967: 366; Francoeur, 1975: 264; Francoeur, 1977b: 207; Yensen, et al. 1977: 184; Smith, D.R. 1979: 1426; Allred, 1982: 456; Wheeler, G.C. & Wheeler, J. 1986g: 60 (in key); DuBois & LaBerge, 1988: 146; Wheeler, G.C., et al. 1994: 305; Bolton, 1995b: 114; Mackay & Mackay, 2002: 298; Coovert, 2005: 167; Hansen & Klotz, 2005: 84; Ellison, et al. 2012: 123; Mackay, 2019: 277 (redescription).
- Senior synonym of pictus: Forel, 1899c: 130; Wheeler, W.M. 1910d: 340; Wheeler, W.M. 1917c: 27; Creighton, 1950a: 369; Smith, M.R. 1951a: 839; Smith, D.R. 1979: 1427; Bolton, 1995b: 114; Mackay, 2019: 278.
- Senior synonym of rubens: Creighton, 1950a: 370; Smith, D.R. 1979: 1427; Bolton, 1995b: 114; Mackay, 2019: 278.
- Distribution: Canada, U.S.A.
- pictus. Camponotus ligniperdus var. pictus Forel, 1886f: 141.
- [First available use of Camponotus herculeanus r. ligniperdus var. pictus Forel, 1879a: 59 (w.q.m.) U.S.A. (Illinois, Wisconsin), MEXICO; unavailable (infrasubspecific) name.]
- Type-material: syntype workers, syntype queens, syntype males (numbers not stated).
- Type-localities: U.S.A.: Illinois (no collector’s name) (ex coll. H. de Saussure), U.S.A.: Wisconsin, Oshkosh (O. Stoll), Mexico: (no further data) (received from Emery).
- Type-depository: MHNG.
- As unavailable (infrasubspecific) name: Emery, 1893i: 674; Emery, 1896d: 372 (in list); Wheeler, W.M. 1905f: 402.
- Subspecies of herculeanus: Mayr, 1886d: 420; Cresson, 1887: 255.
- Subspecies of ligniperda: Dalla Torre, 1893: 240.
- Junior synonym of novaeboracensis: Forel, 1899c: 130; Wheeler, W.M. 1910d: 340; Wheeler, W.M. 1917c: 27; Creighton, 1950a: 369; Smith, M.R. 1951a: 839; Smith, D.R. 1979: 1427; Bolton, 1995b: 117; Mackay, 2019: 278.
- rubens. Camponotus (Camponotus) herculeanus var. rubens Emery, 1925b: 73.
- [First available use of Camponotus herculeanus subsp. ligniperdus var. rubens Wheeler, W.M. 1906a: 41 (q.m.) U.S.A. (Maine, Michigan); unavailable (infrasubspecific) name.]
- Type-material: 7 syntype queens, 1 syntype male.
- Type-localities: 2 queens U.S.A.: Maine, Norway (S.J. Smith), 1 queen, 1 male U.S.A.: Maine, Bethel (A.M. Edwards), 4 queens U.S.A.: Michigan, 1864 (Clark).
- Type-depository: MCZC.
- As unavailable (infrasubspecific) name: Wheeler, W.M. 1906b: 24; Wheeler, W.M. 1910d: 341; Wheeler, W.M. 1910g: 571; Wing, 1939: 163; Smith, M.R. 1951a: 842; Smith, M.R. 1958c: 161.
- Junior synonym of novaeboracensis: Creighton, 1950a: 370; Smith, D.R. 1979: 1427; Bolton, 1995b: 121; Mackay, 2019: 278.
Type Material
Camponotus herculeanus ligniperda var. rubens: 2 cotype females, 1 cotype male, Main, Bothel, A Edwards (1 q, 1 m MCZC # 21446), Michigan, 1864, C. Clark (1 q MCZC # 21446) [all seen]. Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Description
Major worker measurements (mm): HL 2.08 - 2.92, HW 2.12 - 3.22, SL 1.98 - 2.32, EL 0.48 - 0.61, CL 0.65 - 0.99, CW 0.89 - 1.10, WL 2.54 - 3.62, FFL 1.70 - 2.06, FFW 0.54 - 0.68. Indices: CI 102 - 110, SI 79 - 95, CLI 111 - 137, FFI 32 - 33.
Erect and suberect setae present on clypeus, along frontal carinae and tip of scape, absent on side of head, on cheek, posterior lateral corner of head and scape, few erect and suberect setae on ventral surface of head, scattered on dorsum of mesosoma, petiole and all surfaces of gaster, absent on tibiae, except for double row on flexor surface, especially well-developed near tibial spur; appressed pubescence sparse and scattered on head, dorsum of mesosoma and dorsum of gaster, abundant on tibiae, few setae touch adjacent setae on any surface.
Head with dense, fine punctures and with scattered larger punctures, mesosoma coriaceous, gaster with fine, transverse striolae, with scattered larger punctures which bear decumbent setae.
Head and gaster black, mesosoma and legs red; head occasionally red.
Minor worker measurements (mm): HL 1.18 - 1.64, HW 1.02 - 1.44, SL 1.24 - 1.68, EL 0.36 - 0.40, CL 0.34 - 0.49, CW 0.51 - 0.76, WL 1.66 - 2.24, FFL 0.96 - 1.46, FFW 0.34 - 0.43. Indices: CI 86 - 88, SI 102 - 105, CLI 152 - 156, FFI 29 - 35.
Similar to major worker, except eyes nearly reach sides of head, head oval-shaped, scapes extending nearly ½ length past posterior lateral corner of head, pilosity, sculpture and color as in major worker.
Female measurements (mm): HL 2.70 - 2.86, HW 2.88 - 3.06, SL 2.16 - 2.22, EL 0.63 - 0.73, CL 0.89 - 0.98, CW 1.00 - 1.28, WL 4.26 - 5.02, FFL 2.16 - 2.26, FFW 0.66 - 0.74. Indices: CI 106 - 108, SI 78 - 80, CLI 113 - 131, FFI 31 - 33.
Mandible with 5 teeth; sides of head nearly straight, converging anteriorly, posterior margin convex, posterior lateral corners slightly angulate; eyes reaching to within less than 1 minimum diameter of side of head; scape extending about 1 funicular segment past posterior lateral corner of head; mesosoma massive; petiole narrow in profile, apex sharp.
Erect and suberect setae, and appressed pubescence as in major worker, sculpture as in major worker.
Color as in major worker, except mesosoma, petiole and legs dark red, or entire ant may be black.
Male measurements (mm): HL 1.58 - 1.60, HW 1.46 - 1.52, SL 1.72 - 1.76, EL 0.53 - 0.54, CL 0.43 - 0.44, CW 0.68 - 0.73, WL 3.22 - 3.50, FFL 2.14 - 2.24, FFW 0.41 - 0.51. Indices: CI 92 - 95, SI 108 - 111, CLI 159 - 166, FFI 19 - 23.
Moderate sized, black specimen, similar to most others in the genus, except anterior edge of clypeus concave.
References
- Mackay, W.P. 2019. New World Carpenter Ants of the Hyperdiverse genus Camponotus. Volume 1. Introduction, keys to the subgenera and species complexes and the subgenus Camponotus: 412 pp. Lambert Academic Publishing.
- Buren, W. F. 1944a. A list of Iowa ants. Iowa State Coll. J. Sci. 18: 277-312 (page 293, Variety/subspecies of herculeanus)
- 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 369, revived status as species, page 370, senior synonym of rubens)
- Dalla Torre, K. W. von. 1893. Catalogus Hymenopterorum hucusque descriptorum systematicus et synonymicus. Vol. 7. Formicidae (Heterogyna). Leipzig: W. Engelmann, 289 pp. (page 247, junior synonym of pennsylvanicus)
- Ellison A. M., N. J. Gotelli, E. J. Farnsworth, and G. D. Alpert. 2012. A Field Guide to the Ants of New England. Yale University Press. 416 pages.
- Emery, C. 1896j. Saggio di un catalogo sistematico dei generi Camponotus, Polyrhachis e affini. Mem. R. Accad. Sci. Ist. Bologna (5)5:363-382 (page 372, junior synonym of pennsylvanicus)
- Emery, C. 1925e. I Camponotus (Myrmentoma) paleartici del gruppo lateralis. Rend. Sess. R. Accad. Sci. Ist. Bologna Cl. Sci. Fis. (n.s.) 29: 62-72 (page 72, Combination in C. (Camponotus), Variety/subspecies of herculeanus)
- Fitch, A. 1855 [1854]. Report [upon the noxious and other insects of the State of New-York]. Trans. N. Y. State Agric. Soc. 14: 705-880 (page 52, worker described)
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References based on Global Ant Biodiversity Informatics
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