Acanthomyrmex ferox

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Acanthomyrmex ferox
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Crematogastrini
Genus: Acanthomyrmex
Species group: luciolae
Species: A. ferox
Binomial name
Acanthomyrmex ferox
Emery, 1893

Acanthomyrmex ferox casent0178570 profile 1.jpg

Acanthomyrmex ferox casent0178570 dorsal 1.jpg

Specimen labels

Synonyms

A colony of nearly fifty workers was collected in southern Borneo nesting in leaf litter in disturbed primary rainforest (Moffett, 1985).

Identification

Moffett (1986) - Petiolar node of both worker castes with long, dorsally directed lateral spines, and postpetiole with a high, rounded node. Minor worker with conspicuous alveolate sculpture.

Keys including this Species

Distribution

Latitudinal Distribution Pattern

Latitudinal Range: 5.016666667° to 3.698055556°.

 
North
Temperate
North
Subtropical
Tropical South
Subtropical
South
Temperate

Distribution based on Regional Taxon Lists

Indo-Australian Region: Borneo, Indonesia, Malaysia (type locality), Singapore.
Oriental Region: Thailand.

Distribution based on AntMaps

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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.
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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.
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Biology

Soldiers have specialized morphological traits that allow two distinct functions: (1) trophic eggs are produced in ovaries (6 ovarioles) that are the same as in queens (Gobin & Ito 2000); (2) mandibles are modified in shape to crush fig seeds, just as in queens. A. ferox colonies (n=49) have 25±11 workers and 2.6±1.5 soldiers (Gobin & Ito 2000).

Acanthomyrmex ferox, small natural colony with two soldiers, workers and the queen looking into the picture from below. Scattered about the floor of the nest are fig seeds, which serve as food to the ants. 1-II-1998 Ulu Gombak, leg. A. Buschinger.

Ito, Gobin and Hashim (2017) - Foragers can be found on the forest floor and on low vegetation, typically in gaps and forest edges where sunlight reaches the ground (Ulu Gombak field station, Peninsular Malaysia). Nests occur in small dead twigs and accumulated dead leaves. Fig seeds were collected by the workers with field observations revealing the source of these seeds were from bird droppings. In the laboratory workers would also harvest fig seeds when offered, suggesting the seeds would be collected if found independent of bird feces.

Life History Traits

  • Queen type: alate (Yamada et al. 2018, Moffett 1986, Gobin and Ito 2000 and 2003)

Castes

Worker

Images from AntWeb

Acanthomyrmex ferox casent0178572 head 1.jpgAcanthomyrmex ferox casent0178572 profile 1.jpgAcanthomyrmex ferox casent0178572 dorsal 1.jpgAcanthomyrmex ferox casent0178572 label 1.jpg
Worker. Specimen code casent0178572. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by MCZ, Cambridge, MA, USA.

Queen

Images from AntWeb

Acanthomyrmex ferox casent0178573 head 1.jpgAcanthomyrmex ferox casent0178573 profile 1.jpgAcanthomyrmex ferox casent0178573 profile 2.jpgAcanthomyrmex ferox casent0178573 dorsal 1.jpgAcanthomyrmex ferox casent0178573 label 1.jpg
Queen (alate/dealate). Specimen code casent0178573. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by MCZ, Cambridge, MA, USA.

Male

Images from AntWeb

Acanthomyrmex ferox casent0178571 head 1.jpgAcanthomyrmex ferox casent0178571 profile 1.jpgAcanthomyrmex ferox casent0178571 profile 2.jpgAcanthomyrmex ferox casent0178571 dorsal 1.jpgAcanthomyrmex ferox casent0178571 label 1.jpg
Worker. Specimen code casent0178571. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by MCZ, Cambridge, MA, USA.

AcanthomyrmexEconomo-header (arilab.unit.oist.jp).png  X-ray micro-CT scan 3D model of Acanthomyrmex ferox (minor worker) prepared by the Economo lab at OIST.

Acanthomyrmex workers are divided into two different subcastes, so-called minor and major workers. These species are mostly seed predators and the big-headed major workers crush the seeds with their powerful mandibles. See on Sketchfab. See list of 3D images.

AcanthomyrmexEconomo-header (arilab.unit.oist.jp).png  X-ray micro-CT scan 3D model of Acanthomyrmex ferox (major worker) prepared by the Economo lab at OIST.

Acanthomyrmex workers are divided into two different subcastes, so-called minor and major workers. These species are mostly seed predators and the big-headed major workers crush the seeds with their powerful mandibles. See on Sketchfab. See list of 3D images.

Nomenclature

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

  • ferox. Acanthomyrmex ferox Emery, 1893f: 245 (footnote), pl. 6, fig. 11 (w.) WEST MALAYSIA.
    • Type-material: syntype minor workers (number not stated).
    • Type-locality: Malaysia: Malacca, Perak (no collector’s name) (received from Staudinger & Bang-Haas).
    • Type-depositories: MHNG, MSNG.
    • [Acanthomyrmex ferox Emery, 1893a: cclxxvi. Nomen nudum.]
    • Moffett, 1986c: 72 (s.q.m.).
    • Status as species: Emery, 1900d: 678; Emery, 1924d: 235; Chapman & Capco, 1951: 115; Moffett, 1985a: 165; Moffett, 1986c: 70 (redescription); Bolton, 1995b: 53; Jaitrong & Nabhitabhata, 2005: 10; Pfeiffer, et al. 2011: 44; Yamada, Ito, et al. 2018: 10; Jaitrong & Asanok, 2019: 133 (in key); Khachonpisitsak, et al. 2020: 78; Wang, W.Y., Soh, et al. 2022: 68.
    • Senior synonym of dyak: Moffett, 1986c: 70; Bolton, 1995b: 53.
    • Distribution: Indonesia (Kalimantan, Sumatra), Malaysia (Peninsula, Sabah, Sarawak), Singapore, Thailand.
  • dyak. Acanthomyrmex dyak Wheeler, W.M. 1919e: 86 (s.w.) BORNEO (East Malaysia: Sarawak).
    • Type-material: 1 syntype major worker, 2 syntype minor workers.
    • Type-locality: Malaysia: Sarawak, Kuching (J. Hewitt).
    • Type-depository: MCZC.
    • Status as species: Chapman & Capco, 1951: 115.
    • Junior synonym of ferox: Moffett, 1986c: 70; Bolton, 1995b: 53.

Description

Worker

Moffett (1986) - Minor. The two syntypes measure HW 1.06 to 1.12, HL 1.00 to 1.05 (CI 106 to 107), ML 0.83 (MI 83), SL 1.26 to 1.28 (SI 114 to 120), EL 0.20 to 0.21, HFL 1.38 to 1.39 (FLI 132 to 139; FWI 19 to 20) mm.

Head shape as in Acanthomyrmex notabilis, i.e., virtually rounded across posterior margin in full-face view, although slightly flattened or with a trace of a concavity mesad. Maximum head width virtually the same above and below eyes. Cephalic sculpture best described as areolate or alveolate rather than foveate, as the foveae have angular walls and are separated by thin partitions; longer hairs on dorsum of head extend 0.15 mm. Clypeal index 91 to 93. Feeble lobe present on each side of medial clypeal hair; lateral clypeal hairs not in a well-defined fovea. Clypeus virtually smooth, and without two longitudinal rugae present to demarcate a medial clypeal region. Mandibles lacking a ventral tooth.

Spines on trunk virtually straight (propodeal spines with a slight curvature caudad); pronotal spines hairy, and consistently longer than those on propodeum. Pronotal angle drawn out into a feeble tooth (indistinct or absent in some other specimens and on one side of a syntype). Propodeal declivity bordered on each side by a single rugum, as described for Acanthomyrmex crassispinus.

Node of petiole as in figure, PWI wide (120 and 138). Anterior peduncle of petiole relatively short and deep, and with lateral and sublateral hairs; subpetiolar declivity present. Postpetiole smooth (although with feeble foveae on node); with convex lateral margins in dorsal view (rather than rectangular), and almost as long as it is wide. Postpetiole having a distinctive high, rounded node with scattered hairs. Dorsal surface of gaster hairy, but with hair density sparser than in most other luciolae group species. Femora hairy, and with ventral surfaces only feebly concave. Orange yellow, with legs and gaster lighter and with more yellow.

Major. Three Sarawak majors from two series (single major from Peninsular Malaysia very similar): HW 2.42 to 2.58, HL 2.45 to 2.48 (CI 99 to 104), SL 1.20 to 1.25 (SI 47 to 52), EL 0.26 to 0.28, HFL 1.54 to 1.56 (FLI 63 to 68; FWI 20) mm. Frons costate up to level of scrobes (and laterally up to level of eyes); vertex relatively densely foveate (comparison of specimens suggests the foveae become denser and more deeply impressed in progressively smaller majors). No distinct cephalic hollow. No darkly pigmented streak dorsad on head; wide medial sulcus conspicuous, low on face. Forward margin of clypeus with a medial projection. Propodeal spines long, as in minors but thicker at bases. Pronotal angle lacking the feeble tooth characteristic of the minor caste.

Queen

Moffett (1986) - Three queens (from Peninsular Malaysia, Sarawak, and Kalimantan) measure HW 1.86 to 2.30, HL 1.54 to 1.83 (CI 121 to 126), ML 1.08 to 1.20 (MI 65 to 70), SL 1.10 to 1.21 (SI 52 to 59), EL 0.28 to 0.33, HFL 1.53 to 1.68 (FLI 92 to 97; FWI 20 to 21) mm.

Head broad, with lateral margins divergent, and widest near vertex; posterior margin slightly concave mesad. Head with narrow, wavy longitudinal rugae, forming foveae behind level of ocelli and laterally; foveae feeble beneath head. Medial sulcus narrow but conspicuous beneath ocelli. Scrobes prominent, as in majors. Clypeus smooth, with projecting medial lobe as in major. Trunk irregularly rugose laterally (especially on propodeum), smoothest on anepisternum and pronotum. Dorsum with numerous foveae, and with rugae extending forward onto mesonotum from its posterior border. Posterior margin of scutellum with short, stout horns laterally. Propodeal spines short and stout, projecting caudad. Anterior peduncle of petiole short and deep; node of petiole broad, with lateral spines greatly shortened relative to worker castes. Postpetiole narrower than in workers, more than 50% wider than long in dorsal view. Petiole and postpetiole with more pilosity than in workers, but otherwise pilosity similar to workers.

Male

Moffett (1986) - Measurements of five specimens from southern Kalimantan (male from Peninsular Malaysia very similar): HW 0.93 to 1.03, HL 0.76 to 0.82 (CI 123 to 128), ML 0.46 to 0.51 (Ml 56 to 64), SL 0.56 to 0.63 (SI 57 to 61), EL 0.30 to 0.32 mm.

Head broad, widest immediately above eyes; vertex broad, posterior margin of head feebly concave. Head sculptured as in minor workers but less regular and much more feeble; pilosity long, rising 0.25 mm dorsally. Clypeus irregularly longitudinally rugose, forward margin lacks projecting lobes. Trunk as described for queen, but propodeal spines lacking; feebly and irregularly rugose dorsally with only traces of foveate sculpture. Both petiole and postpetiole with low, rounded nodes; postpetiole somewhat longer than wide in dorsal view. Jet black, with legs and gaster dark brown and mandibles dark yellowish orange.

Height of pilosity variable, with the longer hairs dorsally on the head extending about 0.15 mm in the syntypes and in the specimens from Kalimantan, Pahang (Malaysia) and the Gombak (Malaysia) specimen collected by Imai, but shorter (0.08 to 0.10 mm) in other series. Most of the workers with shorter cephalic pilosity have relatively sparse (and very short) pilosity on their gasters, and some also lack pilosity on their pronotal spines.

The traces of very fine rugulose sculpture present on the lateral surfaces of the mandibles of most Acanthomyrmex minor workers is generally absent in Acanthomyrmex ferox, although this microsculpture can be discerned in the types. Petiolar node with spine length and curvature somewhat variable, PWI 105 to 143. Postpetiole of all major workers and some minors (i.e., those from Lampongs and Sarawak) with conspicuous foveae on node, as in individual in figure. Femora sometimes more concave beneath than in syntypes, particularly in the Bolton specimens from Sarawak and the Perak (Malaysia) worker. Color in most specimens darker than in syntypes, reddish orange.

Acanthomyrmex dyak minor syntypes (HW 1.00 and 1.04 mm) very similar to other A. ferox material; major syntype small (HW 2.28 mm), but not as small as the Sabah major (HW 1.98 mm); otherwise very similar to the Sarawak specimens described above. Tooth lacking at pronotal angle in both castes. Femora flattened or at most feebly concave beneath.

Type Material

Moffett (1986) - Peninsular Malaysia: Perak, two minor workers (M. M. Staudinger, Museo Civico di Storia Naturale, Genoa and Musee d'Histoire Naturelle Genève [examined]).

References

References based on Global Ant Biodiversity Informatics

  • Chapman, J. W., and Capco, S. R. 1951. Check list of the ants (Hymenoptera: Formicidae) of Asia. Monogr. Inst. Sci. Technol. Manila 1: 1-327
  • Eguchi K., and S. Yamane. 2003. Species diversity of ants (Hymenoptera, Formicidae) in a lowland rainforest, northwestern Borneo. New Entomol. 52(1,2): 49-59.
  • Emery C. 1893. [Untitled. Introduced by: "M. C. Emery, de Bologne, envoie les diagnoses de cinq nouveaux genres de Formicides".]. Bulletin Bimensuel de la Société Entomologique de France 1892: cclxxv-cclxxvii.
  • Emery C. Formiche raccolte da Elio Modigliani in Sumatra, Engano e Mentawei. Annali del Museo Civico di Storia Naturale 40: 661-722.
  • Emery, C. "Formiche raccolte da Elio Modigliani in Sumatra, Engano e Mentawei." Annali del Museo Civico di Storia Naturale Giacomo Doria (Genova) (2) 20, no. 40 (1900): 661-722.
  • Fayle T.M., Bakker, L., Cheah, C., Ching, T.M., Davey, A., Dem, F., Earl, A., Huaimei, Y., Hyland, S., Johansson, B., Ligtermoet, E., Lim, R., Lin, L.K., Luangyotha, P., Martins, B.H., Palmeirim, A.F., Paninhuan, S., Rojas, S.K., Sam, L., Sam, P.T.T., Susanto, D., Wahyudi, A., Walsh, J., Weigl, S., Craze, P.G., Jehle, R., Metcalfe, D. & Trevelyan, R. 2011. A positive relationship between ant biodiversity (Hymenoptera: Formicidae) and rate of scavenger-mediated nutrient redistribution along a disturbance gradient in a south-east Asian rain forest. Myrmecological News 14: 5-12.
  • Gillison A.N. 2000. Above ground biodiversity assesment working group summary report 1996-99: Impact of different land uses on biodiversity and social indicators. ASB Working Group Report, ICRAF, Nairobi, 160pp. http://www.asb.cgiar.org/PDFwebdocs/ASB Biodiversity Report.pdf
  • Hashimoto Y., and M. Mohamed. 2011. Ground-dwelling ant diversity in Maliau Basin, Borneo: evaluation of hand-sorting methods to estimate ant diversity. Tropics 19(2): 85-92.
  • Jaitrong W., and T. Ting-Nga. 2005. Ant fauna of Peninsular Botanical Garden (Khao Chong), Trang Province, Southern Thailand (Hymenoptera: Formicidae). The Thailand Natural History Museum Journal 1(2): 137-147.
  • Kishimoto-Yamata K., F. Hyodo, M. Matsuoka, Y. Hashimoto, M. Kon, T. Ochi, S. Yamane, R. Ishii, and T. Itioka. 2012. Effects of remnant primary forests on ant and dung beetle species diversity in a secondary forest in Sarawak, Malaysia. Journal of Insect Conservation DOI 10.1007/s10841-012-9544-6
  • Mezger D., and M. Pfeiffer. 2011. Partitioning the impact of abiotic factors and spatial patterns on species richness and community structure of ground ant assemblages in four Bornean rainforests. Ecography 34: 39-48.
  • Mezger D., and M. Pfeiffer. 2011. Partitioning the impact of abiotic factors and spatial patterns on species richness and community structure of ground assemblages in four Bornean rainforest. Ecography 34: 39-48.
  • Moffett M.W. 1985. Behavioral notes on the asiatic harvesting ants Acanthomyrmex notabilis and A. ferox. Psyche 92: 165-180.
  • Moffett, M. 1986. Revision of the myrmicinae genus Acanthomyrmex (Hymenoptera: Formicidae). Bulletin of the Museum of Comparative Zoology 151(2):55-89.
  • Moffett, M. W. 1986. Revision of the myrmicine genus Acanthomyrmex (Hymenoptera: Formicidae). Bulletin of the Museum of Comparative Zoology 151:55-89.
  • Ohasi M., Y. Maekawa, Y. Hashimoto, Y. Takematsu, S. Hasin, and S. Yamane. 2017. CO2 emission from subterranean nests of ants and termites in a tropical rain forest in Sarawak, Malaysia. Applied Soil Ecology 117–118: 147–155.
  • Pfeiffer M., D. Mezger, and J. Dyckmans. 2013. Trophic ecology of tropical leaf litter ants (Hymenoptera: Formicidae) - a stable isotope study in four types of Bornean rain forest. Myrmecological News 19: 31-41.
  • Pfeiffer M., and D. Mezger. 2012. Biodiversity Assessment in Incomplete Inventories: Leaf Litter Ant Communities in Several Types of Bornean Rain Forest. PLoS ONE 7(7): e40729. doi:10.1371/journal.pone.0040742
  • Pfeiffer M., and D. Mezger. 2012. Biodiversity Assessment in Incomplete Inventories: Leaf Litter Ant Communities in Several Types of Bornean Rain Forest. PLoS ONE 7(7): e40729. doi:10.1371/journal.pone.0040962
  • Pfeiffer M., and D. Mezger. 2012. Biodiversity Assessment in Incomplete Inventories: Leaf Litter Ant Communities in Several Types of Bornean Rain Forest. PLoS ONE 7(7): e40729. doi:10.1371/journal.pone.0041060
  • Pfeiffer M.; Mezger, D.; Hosoishi, S.; Bakhtiar, E. Y.; Kohout, R. J. 2011. The Formicidae of Borneo (Insecta: Hymenoptera): a preliminary species list. Asian Myrmecology 4:9-58
  • Sukimin S., M. Mohamed, and H. Aris. 2010. Ant diversity of Maliau Basin Conservation Area, Sabah, Malaysia. Journal of Tropical Biology and Conservation 6:89-101.
  • Wheeler W. M. 1919. The ants of Borneo. Bulletin of the Museum of Comparative Zoology 63:43-147.
  • Woodcock P., D. P. Edwards, R. J. Newton, C. Vun Khen, S. H. Bottrell, and K. C. Hamer. 2013. Impacts of Intensive Logging on the Trophic Organisation of Ant Communities in a Biodiversity Hotspot. PLoS ONE 8(4): e60756. doi:10.1371/journal.pone.0060756
  • Woodcock P., D. P. Edwards, T. M. Fayle, R. J. Newton, C. Vun Khen, S. H. Bottrell, and K. C. Hamer. 2011. The conservation value of South East Asia's highly degraded forests: evidence from leaf-litter ants. Phil. Trans. R. Soc. B. 366: 3256-3264.
  • Wriedt J., D. Mezger, L. Chong, and M. Pfeiffer. 2008. Observations on the foraging behaviour of Myrmicaria brunnea subcarinata (Smith) (Hymenoptera: Formicidae) in a tropical rainforest in Sarawak (Malaysia). Asian Myrmecology 2: 109-120.
  • Yamane S., T. Itino, and A.R. Nona. 1996. Ground ant fauna in a Bornean dipterocarp forest. Raffles Bulletin of Zoology 44(1): 253-262.
  • Yamane S.; Nona, A. R. 1994. Ants from Lambir Hills National Park, Sarawak. Pp. 222-226 in: Inoue, T.; Hamid, A. A. (eds.) 1994. Plant reproductive systems and animal seasonal dynamics. Long-term study of dipterocarp forests in Sarawak. Kyoto: Center for Ecological Research, Kyoto University, vii + 255 pp.