Polyrhachis mucronata

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Polyrhachis mucronata
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Formicinae
Tribe: Camponotini
Genus: Polyrhachis
Subgenus: Myrmhopla
Species: P. mucronata
Binomial name
Polyrhachis mucronata
Smith, F., 1859

Polyrhachis cyrtomyrmoides castype06934 profile 1.jpg

Polyrhachis cyrtomyrmoides castype06934 dorsal 1.jpg

Specimen labels

Subspecies
Synonyms

Colonies of P. mucronata build nests the leaves of rainforest trees and shrubs, using mostly larval silk combined with leaf fragments and other vegetation debris (see image below).

Identification

Kohout (2010) - Among the Australian species of Myrmhopla, Polyrhachis mucronata is very distinct, however, it superficially resembles some species of the subgenus Cyrtomyrma. Despite their general similarity and identical nesting habits, P. mucronata can be easily distinguished from Cyrtomyrma species by the form of its petiole. The petiolar node in P. mucronata is columnar and armed with two, more-or-less horizontal, posteriorly directed spines that conform to the shape of the anterior gaster. The petiole also bears a pair of short, intercalary teeth. In contrast, in Cyrtomyrma species, the petiole is scale-like and armed with four teeth or spines of various configurations. Additionally, all Australian Cyrtomyrma species have a distinct posterolateral carina separating the gena from the ventral parts of the head. This carina is lacking in P. mucronata-group species. The two groups also differ in their immature stages with the pupae of Myrmhopla species being enclosed in cocoons, while in Cyrtomyrma species the pupae are naked (Kohout, 2006b).

Keys including this Species

Distribution

Polyrhachis mucronata ranges from the islands of eastern Indonesia and New Guinea south to northern Queensland where it reaches the southern limit of its distribution. It is a relatively common species in the monsoon rainforests of Cape York Peninsula and the lowland rainforests of the Wet Tropics.

Latitudinal Distribution Pattern

Latitudinal Range: 6.734778° to -18.35°.

 
North
Temperate 		North
Subtropical 		Tropical South
Subtropical 		South
Temperate

Distribution based on Regional Taxon Lists

Australasian Region: Australia.
Indo-Australian Region: Indonesia (type locality), New Guinea, Philippines.

Distribution based on AntMaps

AntMapLegend.png

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

Polyrhachis mucronata nest

Castes

Males and immature stages (eggs, larvae and pupae) deposited in QM spirit collection.

Images from AntWeb

Polyrhachis cyrtomyrmoides castype06934 head 2.jpg
Syntype of Polyrhachis cyrtomyrmoides. Worker. Specimen code castype06934. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.

Nomenclature

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

  • mucronata. Polyrhachis mucronatus Smith, F. 1859a: 140 (w.) INDONESIA (Aru I.). Combination in P. (Myrmhopla): Emery, 1925b: 196. Senior synonym of cyrtomyrmoides: Kohout, 2010: 182. Current subspecies: nominal plus janthinogaster, japensis.
  • cyrtomyrmoides. Polyrhachis (Myrmhopla) cyrtomyrmoides Donisthorpe, 1947d: 195 (w.q.) NEW GUINEA. Junior synonym of mucronata: Kohout, 2010: 1832.

Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.

Kohout (2010) - When describing Polyrhachis cyrtomyrmoides, Donisthorpe (1947: 195) emphasised its close resemblance to ants of the subgenus Cyrtomyrma but failed to note its remarkable similarity to P. mucronata. I had the opportunity to examine the syntypes of P. cyrtomyrmoides, supplemented by additional specimens in the CASC collection (Maffin Bay, 17.vi.1944, E.S. Ross). Their comparison with the holotype of P. mucronata (OXUM) and abundant material of that species from New Guinea and Australia (ANIC, BMNH, BPBM, MCZC and QM) revealed that the two species were very similar. As noted earlier by Kohout (2000: 206), the Australian and New Guinean populations of P. mucronata differ somewhat from the holotype, with some specimens from Australia being remarkably close to those of P. cyrtomyrmoides, sharing the rather highly polished appearance which is typical of the latter species. However, the density of the generally fine reticulate-punctate sculpturation varies not only between different populations, but also to some extent between specimens of a single colony. The colour of the legs also varies, generally being a lighter red in Australian specimens and a darker, reddish-brown in most of New Guinean specimens. In addition, the eyes vary in the degree of their convexity with specimens from the Wet Tropics having the eyes simply convex, similar to those in P. cyrtomyrmoides, while the eyes in specimens from the mid and northern Cape York Peninsula are virtually protuberant. When considered individually, specimens of some populations appear quite distinct, however, when all the available material from the whole distribution range is compared, no consistent differences between P. cyrtomyrmoides and P. mucronata are evident. I therefore believe that the separate specific status of the former is not justified and consider them conspecific.

Description

Worker

Kohout (2010) - (holotype cited first) TL c. 5.55, 5.34-6.50; HL 1.43, 1.40-1.65; HW 1.17, 1.12-1.31; CI 82, 76-82; SL 1.84, 1.65-2.12; SI 157, 146-164; PW 1.00, 0.94-1.15; MTL 1.93, 1.81-2.31 (31 measured).

Anterior clypeal margin medially with shallow flange, flanked laterally by acute angles. Clypeus with poorly defined median carina; clypeus in profile straight anteriorly, posteriorly rounding into moderately impressed basal margin. Frontal carinae sinuate with moderately raised margins. Sides of head in front of eyes weakly convex converging towards mandibular bases; behind eyes sides rounding into convex occipital margin. Eyes relatively large and convex, in full face view clearly exceeding lateral cephalic outline. Ocelli lacking. Mesosoma immarginate. Pronotal humeri armed with short, acute teeth. Promesonotal suture distinct; mesonotum virtually flat in profile. Mesopleural process a blunt lobe; metanotal groove indicated as a thin, bowed line. Propodeal dorsum very short, armed with rather strong, obliquely directed, diverging, acute spines; inner borders of spines continued medially for a short distance, but failing to meet, propodeal dorsum descending into relatively high, oblique declivity in uninterrupted line. Petiole columnar, dorsum armed with two strong lateral spines that conform to shape of anterior gaster and two short, acute intercalary teeth medially. Anterior face of first gastral tergite straight, widely rounding onto dorsum of segment.

Mandibles very finely, longitudinally striate with numerous piliferous pits. Head and dorsum of mesosoma and petiole finely reticulate-punctate with sculpturation distinctly coarser on sides of mesosoma; meso- and metapleurae weakly rugose and somewhat wrinkled. Gaster finely shagreened.

Mandibles at masticatory and outer borders with a few, curved, golden hairs. Anterior clypeal margin with several anteriorly directed setae medially and a pair of longer, suberect hairs arising from just behind margin. Tuft of medium length, erect hairs in front of subpetiolar process. Apical segments on dorsum and venter of gaster with a number of semierect, posteriorly directed, golden hairs. Very short, closely appressed pubescence arising from minute punctures and pits, distributed over most body surfaces, more distinct on gastral dorsum.

Body black, polished; mandibular bases, antennal scapes, fore coxae and tarsi black or very dark reddish-brown; mandibular masticatory borders, condylae, apical antennal segments and most of legs, except tarsi, light to medium reddish-brown.

Queen

Kohout (2010) - TL c. 6.95-7.81; HL 1.65-1.75; HW 1.25-1.34; CI 75-77; SL 1.96-2.12; SI 153-160; PW 1.56-1.68; MTL 2.18-2.37 (10 measured).

Very similar to worker with usual differences indicating caste, including three ocelli, complete thoracic structure and wings. Median clypeal carina somewhat more distinct. Pronotal teeth dorsoventrally flattened; mesoscutum in lateral view with anterior margin widely rounding onto flat dorsum; median line bifurcate anteriorly; parapsides rather flat, weakly raised posteriorly; mesoscutellum convex, elevated above dorsal plane of mesosoma; metanotal groove strongly impressed. Propodeal spines shorter than in worker, almost straight; petiolar spines similar to those in worker but shorter. Sculpturation, pilosity, pubescence and colour virtually identical to worker.

Type Material

Kohout (2010) - Holotype worker: INDONESIA: Aru Is. (A. R. Wallace), Oxford University Museum of Natural History (examined).

The following notes on F. Smith type specimens have been provided by Barry Bolton (details):

Polyrhachis mucronatus

Holotype worker in Oxford University Museum of Natural History. Labelled “Aroo” (= Aru I., New Guinea) and with a Donisthorpe type-label.

References

References based on Global Ant Biodiversity Informatics

  • Donisthorpe H. 1947. Some new ants from New Guinea. Annals and Magazine of Natural History (11)14: 183-197.
  • Donisthorpe H. 1948. A third instalment of the Ross Collection of ants from New Guinea. Annals and Magazine of Natural History (11)14: 589-604.
  • Donisthorpe H. 1949. A fifth instalment of the Ross Collection of ants from New Guinea. Annals and Magazine of Natural History (12)1: 487-506.
  • Donisthorpe, Horace. 1943. The Ants of Waigeu Island, North Dutch New Guinea. The Annals and Magazine of Natural History 11 (10): 433-475.
  • Emery C. 1886. Saggio di un catalogo sistematico dei generi Camponotus, Polyrhachis e affini. Memorie della Reale Accademia delle Scienze dell'Istituto di Bologna 5: 363-382
  • Emery C. 1911. Formicidae. Résultats de l'expédition scientifique néerlandaise à la Nouvelle-Guinée en 1903 sous les auspices de Arthur Wichmann. Nova Guinea 5: 531-539.
  • General D. M., and G. D. Alpert. 2012. A synoptic review of the ant genera (Hymenoptera, Formicidae) of the Philippines. Zookeys 200: 1-111.
  • Hashimoto Y., Y. Morimoto, E. S. Widodo, and M. Mohamed. 2006. Vertical distribution pattern of ants in a Bornean tropical rainforest (Hymenoptera: Formicidae). Sociobiology 47(3): 697- 710.
  • Janda M., G. D. Alpert, M. L. Borowiec, E. P. Economo, P. Klimes, E. Sarnat, and S. O. Shattuck. 2011. Cheklist of ants described and recorded from New Guinea and associated islands. Available on http://www.newguineants.org/. Accessed on 24th Feb. 2011.
  • Klimes P., P. Fibich, C. Idigel, and M. Rimandai. 2015. Disentangling the diversity of arboreal ant communities in tropical forest trees. PLoS ONE 10(2): e0117853. doi:10.1371/journal.pone.0117853
  • Kohout R. J. 2000. A review of the distribution of the Polyrhachis and Echinopla ants of the Queensland wet tropics (Hymenoptera: Formicidae: Formicinae). Memoirs of the Queensland Museum 46: 183-209
  • Kohout R. J. 2010. A review of the Australian Polyrhachis ants of the subgenera Myrmhopla Forel and Hirtomyrma subgen. nov. (Hymenoptera: Formicidae: Formicinae). Memoirs of the Queensland Museum - Nature 55:167-204.
  • Kohout R. J., and R. W. Taylor. 1990. Notes on Australian ants of the genus Polyrhachis Fr. Smith, with a synonymic list of the species (Hymenoptera: Formicidae: Formicinae). Memoirs of the Queensland Museum 28: 509-522.
  • Mezger D., and C. S. Moreau. 2015. Out of South-East Asia: phylogeny and biogeography of the spiny ant genus Polyrhachis Smith (Hymenoptera: Formicidae). Systematic Entomology DOI: 10.1111/syen.12163
  • Robson Simon Database Polyrhachis -05 Sept 2014
  • Snelling R. R. 2000. Ants of the Wapoga river area, Irian Jaya, Indonesia. In Mack, Andrew L. and Leeanne E. Alonso (eds.). 2000. A Biological Assessment of the Wapoga River Area of Northwestern Irian Jaya, Indonesia. RAP Bulletin of Biological Assessment 14, Conservation International, Washington, DC.
  • Trainor C.R. and A.N. Andersen. 2010. The ant fauna of Timor and neighbouring islands: potential bridges between the disjunct faunas of South East Asia and Australia. Australian Journal of Zoology 58: 133-144.
  • Trainor C.R., and A.N. Andersen. 2010. The ant fauna of Timor and neighbouring islands: potential bridges between the disjunct faunas of South East Asia and Australia. Australian Journal of Zoology 58: 133-144.
  • Viehmeyer H. 1912. Ameisen aus Deutsch Neuguinea gesammelt von Dr. O. Schlaginhaufen. Nebst einem Verzeichnisse der papuanischen Arten. Abhandlungen und Berichte des Königlichen Zoologischen und Anthropologische-Ethnographischen Museums zu Dresden 14: 1-26.
  • Wheeler, William Morton.1935.Checklist of the Ants of Oceania.Occasional Papers 11(11): 3-56
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