Mycetophylax bigibbosus

Mycetophylax bigibbosus
Scientific classification
Kingdom:	Animalia
Phylum:	Arthropoda
Class:	Insecta
Order:	Hymenoptera
Family:	Formicidae
Subfamily:	Myrmicinae
Tribe:	Attini
Genus:	Mycetophylax
Species:	M. bigibbosus
Binomial name
Mycetophylax bigibbosus (Emery, 1894) Specimen Labels
Synonyms
Cyphomyrmex bigibbosus tumulus Weber, 1938

A rainforest species that nests in rotting wood.

Identification

Kempf (1964) - The head of the bigibbosus worker is strikingly similar to that of Mycetophylax strigatus, but the configuration of the thorax, the pedicel and the gaster shows clearly the conspicuous differences between both species.

Distribution

Known from Brazil and British Guiana.

Latitudinal Distribution Pattern

Latitudinal Range: 11.25° to -2.416667°.

North Temperate	North Subtropical	Tropical	South Subtropical	South Temperate

• Source: AntMaps

Distribution based on Regional Taxon Lists

Neotropical Region: Brazil (type locality), French Guiana, Guyana, Suriname, Trinidad and Tobago.

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.

Estimated Abundance

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

Biology

Explore Fungus Growing  For additional details see Fungus growing ants. A handful of ant species (approx. 275 out of the known 15,000 species) have developed the ability to cultivate fungus within their nests. In most species the fungus is used as the sole food source for the larvae and is an important resource for the adults as well. Additionally, in a limited number of cases, the fungus is used to construct part of the nest structure but is not as a food source. These fungus-feeding species are limited to North and South America, extending from the pine barrens of New Jersey, United States, in the north (Trachymyrmex septentrionalis) to the cold deserts in Argentina in the south (several species of Acromyrmex). Species that use fungi in nest construction are known from Europe and Africa (a few species in the genera Crematogaster, Lasius). The details of fungal cultivation are rich and complex. First, a wide variety of materials are used as substrate for fungus cultivating. The so-called lower genera include species that prefer dead vegetation, seeds, flowers, fruits, insect corpses, and feces, which are collected in the vicinity of their nests. The higher genera include non leaf-cutting species that collect mostly fallen leaflets, fruit, and flowers, as well as the leafcutters that collect fresh leaves from shrubs and trees. Second, while the majority of fungi that are farmed by fungus-feeding ants belong to the family Lepiotaceae, mostly the genera Leucoagaricus and Leucocoprinus, other fungi are also involved. Some species utilise fungi in the family Tricholomataceae while a few others cultivate yeast. The fungi used by the higher genera no longer produce spores. Their fungi produce nutritious and swollen hyphal tips (gongylidia) that grow in bundles called staphylae, to specifically feed the ants. Finally, colony size varies tremendously among these ants. Lower taxa mostly live in inconspicuous nests with 100–1000 individuals and relatively small fungus gardens. Higher taxa, in contrast, live in colonies made of 5–10 million ants that live and work within hundreds of interconnected fungus-bearing chambers in huge subterranean nests. Some colonies are so large, they can be seen from satellite photos, measuring up to 600 m3. Based on these habits, and taking phylogenetic information into consideration, these ants can be divided into six biologically distinct agricultural systems (with a list of genera involved in each category): Nest Construction A limited number of species that use fungi in the construction of their nests. some Crematogaster some Lasius Lower Agriculture Practiced by species in the majority of fungus-feeding genera, including those thought to retain more primitive features, which cultivate a wide range of fungal species in the tribe Leucocoprineae. some Apterostigma Cyatta (1 species) some Cyphomyrmex Kalathomyrmex (1 species) Mycocepurus (6 species) Myrmicocrypta (31 species) Mycetarotes (4 species) Mycetosoritis (2 species) Mycetophylax (21 species) Paramycetophylax (1 species) Xerolitor (1 species) Coral Fungus Agriculture Practiced by species in the Apterostigma pilosum species-group, which cultivate fungi within the Pterulaceae. some Apterostigma Yeast Agriculture Practiced by species within the Cyphomyrmex rimosus species-group, which cultivate a distinct clade of leucocoprineaceous fungi derived from the lower attine fungi. some Cyphomyrmex Generalized Higher Agriculture Practiced by species in several genera of non-leaf-cutting "higher attine" ants, which cultivate a distinct clade of leucocoprineaceous fungi separately derived from the lower attine fungi. Mycetomoellerius (31 species) Paratrachymyrmex (9 species) Sericomyrmex (11 species) Trachymyrmex (9 species) Leaf-Cutter Agriculture A subdivision of higher attine agriculture practiced by species within several ecologically dominant genera, which cultivate a single highly derived species of higher attine fungus. Acromyrmex (56 species) Amoimyrmex (3 species) Atta (20 species) Note that the farming habits of Mycetagroicus (4 species) are unknown. Also, while species of Pseudoatta (2 species) are closely related to the fungus-feeding genus Acromyrmex, they are social parasites, living in the nests of their hosts and are not actively involved in fungus growing. ‎

Kempf (1964) summarized Weber's (1946) account of the synonymized subspecies tumulus:

M. bigibbosus is a rain forest species and seems to prefer high humidities. The nest chambers were found in rotted wood, mostly in excavate cells, but also under bark. The cavity size is variable but averages about 20-25 cc. The fungus garden is mostly sessile, resting on the floor, but variously attached at the sides. Occasionally the chains of fungus garden are also suspended from the ceiling. The substrate is heterogeneous, consisting mainly of yellow to brown particles, often of woody consistency; once even a head of a Dolichoderus ant was used as substrate. Once a worker of Prionopelta punctulata was found inside a nest, preying perhaps on the larvae of M. bigibbosus. The finding of an dealate queen in a tiny fungus garden, with a full grown worker, suggests splitting as a possible means of colony foundation.

Nomenclature

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

• bigibbosus. Cyphomyrmex bigibbosus Emery, 1894c: 226 (w.) BRAZIL.
  • Wheeler, G.C. 1949: 670 (l.).
  • Combination in Mycetophylax: Sosa-Calvo et al., 2017: 9.
  • Senior synonym of tumulus: Kempf, 1972a: 92.
  • See also: Kempf, 1964d: 20.
• tumulus. Cyphomyrmex bigibbosus subsp. tumulus Weber, 1938b: 185 (w.q.m.) GUYANA.
  • Junior synonym of bigibbosus: Kempf, 1964d: 20.
  • Revived from synonymy and raised to species: Weber, 1966: 167.
  • Junior synonym of bigibbosus: Kempf, 1972a: 92.

Description

Worker

Kempf (1964) - Total length 3.2-3.4 mm; head length 0.75-0.83 mm; head width 0.67-0.75 mm; thorax length 0.93-1.04 mm; hind femur length 0.83-0.91 mm. Fuscous reddish brown; head usually darkest; mandibles, coxae, femora and sometimes also thorax light brown. Integument, including antennal scrobe, densely granular and opaque.

Head (fig 2). - Mandibles with 7-8 teeth. Clypeus: anterior border mesially excised; central portion of c1ypeus obliquely raised towards front, with two acute teeth next to origin of frontal lobes. Vertex with a pair of short carinules. Supraocular tumulus blunt, rounded, not prominent. Preocular carinae reaching the gently produced occipital lobes, closing completely the antennal scrobe. Lower border of sides of head carinate. Antennal scapes, in repose, not projecting beyond tip of occipital lobes. Only funicular segments 1 and 10 distinctly longer than broad.

Thorax (fig 16). - Pronotum: the single median tubercle quite distinct, the lateral ones very low and blunt, continued foreward as a faint, often more or less obsolete, margination that separates the pronotal dorsum from the sides: antero-inferior corner acutely dentate. Mesonotum: anterior pair of tubercles prominent and conical, posterior pair very low but distinct and blunt. Mesoepinotal constriction conspicuous but relatively shallow in profile. Epinotum completely rounded and unarmed. Hind femora a little dilated ventrally but not visibly carinate posteriorly at basal third.

Pedicel (fig 16, 30). - Petiole in dorsal view rather longer than broad, anterior corners of node not sharply angulate, dorsal ridges at best vestigial, posterior dorsal border without a raised carinule. Postpetiole, in dorsal view, subquadrate not transverse, with a perpendicular anterior face, a rather flat dorsal face, having the posterior border deeply excised between a pair of prominent horizontal tubercles. Tergum I of gaster strongly vaulted, lacking lateral margination and longitudinal carinae. Hairs minute, appressed, glittering, scattered; quite inconspicuous, on body and appendages.

• 

  Figs. 13-24

• 

  Figs. 25-36

Queen

Kempf (1964) - Total length 3.8 mm; head length 0.84 mm; head width 0.79 mm; thorax length 1.20 mm; hind femur length 0.96 mm. Resembling the worker with the differences of the caste. Differs from Mycetophylax faunulus in the following features: Bicolored, head and gaster fuscous, thorax brown. Occipital lobes much less projecting both in full-face view as in profile, much as in worker. Midpronotal tubercle faint but still distinguishable. Pair of anterior tubercles between arms of Mayrian furrows very low; scutum laterally not deeply furrowed. Paraptera postero-laterally with a short tooth. Posterior scutellar teeth much shorter, about as long as their width at base. Epinotal teeth completely absent. Pedicel as in worker; petiole elongate, with subparallel sides, anterior corners rather rounded; postpetiole with the same deep mesial excision on posterior border, flanked by prominent lobes, as in worker. Gaster bigibbous on anterior third of tergum I.

Male

Weber (1938), as tumulus

Type Material

Kempf (1964) - The lone holotype worker of bigibbosus is in the Emery collection at the "Museo Civico di Storia Naturale", Genova, Italy; not seen. Syntypes of tumulus: 3 workers examined (MCZ, NAW).

References

• Albuquerque, E., Prado, L., Andrade-Silva, J., Siqueira, E., Sampaio, K., Alves, D., Brandão, C., Andrade, P., Feitosa, R., Koch, E., Delabie, J., Fernandes, I., Baccaro, F., Souza, J., Almeida, R., Silva, R. 2021. Ants of the State of Pará, Brazil: a historical and comprehensive dataset of a key biodiversity hotspot in the Amazon Basin. Zootaxa 5001, 1–83 (doi:10.11646/zootaxa.5001.1.1).
• Emery, C. 1894d. Studi sulle formiche della fauna neotropica. VI-XVI. Bull. Soc. Entomol. Ital. 26: 137-241 (page 226, worker described)
• Franco, W., Ladino, N., Delabie, J.H.C., Dejean, A., Orivel, J., Fichaux, M., Groc, S., Leponce, M., Feitosa, R.M. 2019. First checklist of the ants (Hymenoptera: Formicidae) of French Guiana. Zootaxa 4674, 509–543 (doi:10.11646/zootaxa.4674.5.2).
• Kempf, W. W. 1964d. A revision of the Neotropical fungus-growing ants of the genus Cyphomyrmex Mayr. Part I: Group of strigatus Mayr (Hym., Formicidae). Stud. Entomol. 7: 1-44 (page 20, see also)
• Kempf, W. W. 1972b. Catálogo abreviado das formigas da regia~o Neotropical. Stud. Entomol. 15: 3-344 (page 92, Senior synonym of tumulus)
• Sosa-Calvo, J., JesÏovnik, A., Vasconcelos, H.L., Bacci, M. Jr., Schultz, T.R. 2017. Rediscovery of the enigmatic fungus-farming ant "Mycetosoritis" asper Mayr (Hymenoptera: Formicidae): Implications for taxonomy, phylogeny, and the evolution of agriculture in ants. PLoS ONE 12: e0176498 (DOI 10.1371/journal.pone.0176498).
• Weber, N. A. 1946. The biology of the fungus-growing ants. Part IX. The British Guiana species. Rev. Entomol. (Rio de Janeiro). 17:114-172.
• Wheeler, G. C. 1949 [1948]. The larvae of the fungus-growing ants. Am. Midl. Nat. 40: 664-689 (page 670, larva described)

References based on Global Ant Biodiversity Informatics

• Fernández, F. and S. Sendoya. 2004. Lista de las hormigas neotropicales. Biota Colombiana Volume 5, Number 1.
• Franco W., N. Ladino, J. H. C. Delabie, A. Dejean, J. Orivel, M. Fichaux, S. Groc, M. Leponce, and R. M. Feitosa. 2019. First checklist of the ants (Hymenoptera: Formicidae) of French Guiana. Zootaxa 4674(5): 509-543.
• Groc S., J. H. C. Delabie, F. Fernandez, M. Leponce, J. Orivel, R. Silvestre, Heraldo L. Vasconcelos, and A. Dejean. 2013. Leaf-litter ant communities (Hymenoptera: Formicidae) in a pristine Guianese rainforest: stable functional structure versus high species turnover. Myrmecological News 19: 43-51.
• Groc S., J. Orivel, A. Dejean, J. Martin, M. Etienne, B. Corbara, and J. H. C. Delabie. 2009. Baseline study of the leaf-litter ant fauna in a French Guianese forest. Insect Conservation and Diversity 2: 183-193.
• Kempf W. W. 1959. Insecta Amapaensia. - Hymenoptera: Formicidae. Studia Entomologica (n.s.)2: 209-218.
• Kempf W. W. 1964. A revision of the Neotropical fungus-growing ants of the genus Cyphomyrmex Mayr. Part I: Group of strigatus Mayr (Hym., Formicidae). Studia Entomologica 7: 1-44.
• Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
• Kusnezov N. 1953. La fauna mirmecológica de Bolivia. Folia Universitaria. Cochabamba 6: 211-229.
• Mayhe-Nunes A. J., and K. Jaffe. 1998. On the biogeography of attini (Hymenoptera: Formicidae). Ecotropicos 11(1): 45-54.
• Medeiros Macedo L. P., E. B. Filho, amd J. H. C. Delabie. 2011. Epigean ant communities in Atlantic Forest remnants of São Paulo: a comparative study using the guild concept. Revista Brasileira de Entomologia 55(1): 75–78.
• Weber N. A. 1938. The biology of the fungus-growing ants. Part IV. Additional new forms. Part V. The Attini of Bolivia. Rev. Entomol. (Rio J.) 9: 154-206.
• Weber N. A. 1945. The biology of the fungus-growing ants. Part VIII. The Trinidad, B. W. I., species. Revista de Entomologia (Rio de Janeiro) 16: 1-88.
• Weber N. A. 1946. The biology of the fungus-growing ants. Part IX. The British Guiana species. Revista de Entomologia (Rio de Janeiro) 17: 114-172.
• Weber, Neal A. 1968. Tobago Island Fungus-growing Ants (Hymenoptera: Formicidae). Entomological News. 79:141-145.
• Weber, Neal A. 1968. Tobago Island Fungus-growing Ants. Entomological News. 79(6): 141-145.
• Weber, Neil A. 1968. Tobago Island Fungus-growing Ants (Hymenoptera: Formicidae). Entomological News. 79(6):141-145.