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Cyphomyrmex rimosus is a small dull brown to blackish brown ant with deep antennal scrobes, enlarged frontal lobes that obscure the lateral margins of the face, no propodeal spines, an apedunculate petiole, tubercles on the mesosoma, and appressed scale-like hairs. These ants are sometimes difficult to detect on account of their small size, slow movement and tendency to become immobile and even feign death when disturbed. Cyphomyrmex rimosus has a monomorphic worker caste and is considered one of the ‘lower’ attines and cultivates fungus gardens grown on scavenged vegetable matter, dead insects and insect fras. The species is native to the Neotropics, but has established introduced populations in the southern United States and the Galapagos islands. It is not considered a significant pest species in its native or introduced range.// Distribution
Native Range (Snelling & Longino, 1992). Neotropics. Argentina, Brazil, Guinanas, Venezuala.
Introduced Range. Galapagos: Isabella, Santa Cruz. United States (Snelling & Longino, 1992): Alabama, Florida, Georgia, Mississippi.
The species is part of a complex of closely related and highly variable taxa that can be difficult to distinguish (Kempf, 1966 (1965)). Snelling and Longino (1992)revised the C. rimosus group and split it into five subgroups. The rimosus subgroup contains seven species, including C. rimosus and its close relative C. minutus. Both species occur in Florida, but whereas C. rimosus is argued to be introduced on the grounds that it has spread rapidly since it was first detected, Cyphomyrmex minutus is considered native (Deyrup, 1991). Cyphomyrmex minutus was treated as a junior synonym of C. rimosus prior to the revision of Snelling and Longino (1992), so it is difficult to determine which species earlier studies are referring to. For example, many of the Neotropical and North American records in the literature refer to the more widespread C. minutus (Snelling & Longino, 1992).
Cyphomyrmex rimosus usually live in colonies of less than 100 workers, but colonies of over 300 workers have been observed (Murakami & Higashi, 1997). Most colonies are usually monogynous, but there are reports of some polygynous colonies as well (Murakami & Higashi, 1997; Snelling & Longino, 1992). The fungus gardens are composed of yeasts in the unicellular phase rather than in the multicellular, mycelial phase typical of all other attine gardens (Mehdiabadi & Schultz, 2010). In addition to feeding on the yeast fungus grown in their gardens, C. rimosus is also known to take the nectar and sap of plants (Murakami & Higashi, 1997). The queens are reported to practice monandry and semi-claustral nest founding (Mehdiabadi & Schultz, 2010; Tschinkel, 1987). Nests are frequently simple, shallow, impermanent structures under rocks, logs or any other surface, and the species prefers open habitats. Further details of the natural history of C. rimosus, in is given in Mehdiabadi & Schultz (2010), Murakami & Higashi (1997)and Snelling and Longino (1992).
(Source unkown). Anida en raíces de las plantas, bajo piedras, forrajea entre la hojarasca. Es frecuente en áreas ocupadas por Wasmannia auropunctata. Presente en jardines de las viviendas y sitios húmedos.
English translation: Nests in plant roots, under rocks, foraging among the fallen leaves. It is common in areas occupied by Wasmannia auropunctata. Present in gardens of dwellings and wet locations.
Diagnosis among workers of introduced and commonly intercepted ants in the United States. Antenna 11-segmented. Antennal club 2-segmented. Antennal scapes easily extended beyond eye level. Antennal scrobe present and well developed. Eyes medium to large (greater than 5 facets) but distinctly less than half head length. Eyes located below antennal scrobe near midline of head. Frontal lobes obscure face outline between mandible and eye. Posterolateral corners of head unarmed, without spines. Mandibles triangular. Pronotal spines absent. Propodeum lacking spines or teeth, but tubercles are present. Waist 2-segmented. Spongiform not attached to any portion of waist. Dull brown to blackish brown. Surfaces with appressed scale-like hairs.
In the United States, C. rimosus is most likely confused with C. minutus. Snelling and Longino (1992) separate the two species by the following characters. The head width of C. rimosus is greater (0.62 mm vs. 0.56 mm), and in C. rimosus the hairs on first gastral tergite are not completely appressed and separated by less than their own lengths whereas those of C. minutus are closely appressed and usually separated by more than their own lengths.
Among other introduced and commonly intercepted ants in the United States, C. rimosus can be distinguished the enlarged frontal lobes that obscure the lateral margins of the face, 11-segmented antenna, deep antennal scrobes, indistinct antennal club, and lack of propodeal spines. The antennal scrobes and lack of spines separates C. rimosus from other attine genera (Acromyrmex and Atta). Cephalotes species also have enlarged frontal lobes that obscure the lateral face margins, but C. rimosus can be distinguished from them by the eyes which are placed below antennal scrobe near midline of head (as opposed to at or near apex of antennal scrobe in Cephalotes).
Deyrup, M. (1991) Exotic ants of the Florida keys (Hymenoptera: Formicidae). In: Eshbaugh, W.H. (Ed.) Proceedings of the 4th symposium on the natural history of the Bahamas. Bahamian Field Station, San Salvador, Bahamas, pp. 15-22.
Deyrup, M. (2003) An updated list of Florida ants (Hymenoptera: Formicidae). Florida Entomol., 86, 43-48.
Deyrup, M., Davis, L. & Cover, S. (2000) Exotic ants in Florida. Trans. Am. Entomol. Soc., 126, 293-326.
Kempf, W.W. (1966 (1965)) A revision of the Neotropical fungus-growing ants of the genus Cyphomyrmex Mayr. Part II: Group of rimosus (Spinola) (Hym., Formicidae). Stud. Entomol., 8, 161-200.
Mehdiabadi, N.J. & Schultz, R. (2010) Natural history and phylogeny of the fungus-farming ants (Hymenoptera: Formicidae: Myrmicinae: Attini). Myrmecol. News, 13, 37-55.
Murakami, T. & Higashi, S. (1997) Social organization in two primitive attine ants, Cyphomyrmex rimosus and Myrmicocrypta ednaella, with reference to their fungus substrates and food sources. J. Ethol., 15, 17-25.
Snelling, R.R. & Longino, J.T. (1992) Revisionary notes on the fungus-growing ants of the genus Cyphomyrmex rimosus group (Hymenoptera: Formicidae: Attini). In: Quintero, D. & Aiello, A. (Eds.) Insects of Panama and Mesoamerica: selected studies. Oxford University Press, Oxford. xxii + 692 p., pp. 479-494, English summary p. 653, Spanish summary p. 662-663.
Tschinkel, W.R. (1987) Relationship between ovariole number and spermathecal sperm count in ant queens: a new allometry. Ann. Entomol. Soc. Am., 80, 208-211.
|Cyphomyrmex rimosus||Snelling, R. R. & Longino, J. T., 1992, Revisionary notes on the fungus-growing ants of the genus Cyphomyrmex, rimosus-group (Hymenoptera: Formicidae: Attini)., Insects of Panama and Mesoamerica: selected studies., Oxford: Oxford University Press, pp. 479-494: 491, (download)||491||13137|
|Cyphomyrmex longiscapus||Kempf, W. W., 1966, A revision of the Neotropical fungus-growing ants of the genus Cyphomyrmex Mayr. Part II. Group of rimosus (Spinola) (Hym. Formicidae)., Studia Entomologica (N. S.) 8, pp. 161-200: 161-165, (download)||161-165||4580|
|Cyphomyrmex rimosus||Wild, A. L., 2007, A catalogue of the ants of Paraguay (Hymenoptera: Formicidae)., Zootaxa 1622, pp. 1-55: 33, (download)||33||21367|
|Cyphomyrmex rimosus||Forel, A., 1893, Formicides de l'Antille St. Vincent. Récoltées par Mons. H. H. Smith., Transactions of the Entomological Society of London 1893, pp. 333-418: 374-375, (download)||374-375||3948|
|Cyphomyrmex rimosus||Kempf, W. W., 1966, A revision of the Neotropical fungus-growing ants of the genus Cyphomyrmex Mayr. Part II. Group of rimosus (Spinola) (Hym. Formicidae)., Studia Entomologica (N. S.) 8, pp. 161-200: 198, (download)||198||4580|
|Cyphomyrmex rimosus||Kempf, W. W., 1968, A new species of Cyphomyrmex from Colombia, with further remarks on the genus (Hymenoptera, Formicidae)., Revista Brasileira de Biologia 28, pp. 35-41: 40, (download)||40||4586|
Found most commonly in these habitats: 1 times found in deciduous forest, 0 times found in in EXTERRA termite bait stations, 0 times found in litter from sandy roadside with lots of native grasses, 0 times found in relic dune scrub, 0 times found in Black Belt Prairie, 0 times found in in ground termite bait station, 0 times found in litter from pine bases in mixed hardwood-pine coastal woodland, 0 times found in in sandhill, 0 times found in behind beach house, 0 times found in mixed forest near estuary, ...
Found most commonly in these microhabitats: 2 times under rock, 2 times litter, 2 times ex rotten log, 1 times strays in leaf litter, 1 times stray in leaf litter, 1 times stray foragers, 1 times sifting litter, 1 times rainforest, 1 times pine buttress, 1 times on recently felled trees, 1 times on orchids, ...
Collected most commonly using these methods: 0 times Berlese funnel, 0 times Lindgren funnel baited with Typosan, 1 times Malaise trap, 0 times Exterra termite bait station, 0 times Lindgren funnel baited with Typosan and alpha pinene, 1 times pitfall trap, 1 times boxtrap, 6 times direct collection, 4 times hand collecting, 0 times Lindgren funnel, 0 times aspirated, ...
Elevations: collected from 5 - 1100 meters, 404 meters average
Collect Date Range: collected between 1935-02-07 and 2018-11-17
Type specimens: syntype of Cyphomyrmex rimosus: casent0904979; syntype of Cyphomyrmex rimosus curiapensis: casent0901677; syntype of Cyphomyrmex rimosus fuscus: casent0919614; syntype of Meranoplus difformis: casent0901675; type of Cyphomyrmex rimosus: focol1761, focol1762, focol1763; type of Cyphomyrmex rimosus fuscula: focol1770