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Marine life guide of Peru · Balanidae

Giant barnacle

Austromegabalanus psittacus (Molina, 1788)

IUCN status: Not evaluated

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Giant barnacle
Photo: Norero · CC BY-SA 4.0 · Wikimedia Commons

Species account

Summary

Austromegabalanus psittacus is a large acorn barnacle that lives attached to submerged surfaces on the South American Pacific coast; it is reported from southern Peru to southern Argentina [1]. It is a simultaneous hermaphrodite, sessile and gregarious, taken by small-scale fishing in Chile and assessed as a candidate for aquaculture [2],[1].

Identification and similar species

It is a cirripede crustacean with a calcareous shell, large for a balanomorph. In a sample of 100 specimens bought in southern Chilean markets in 2007, mean carino-rostral length was about 36 mm, with a maximum of 50 mm, and carinal height ranged from 67 to 140 mm [1]. The wall plates are built of calcite grains 0.5 to 10 µm across [3].

The genus includes another species, Austromegabalanus nigrescens; a 2008 paper reports both for the first time from New Zealand waters [4]. In northern Chile Austromegabalanus psittacus occurs together with another barnacle, Megabalanus concinnus [5]. The species was originally described as Lepas psittacus by Molina, and the exact year of that publication has caused confusion [6]; the sources consulted write the authority as Molina, 1782 [1] or Molina, 1788 [7].

Distribution and habitat

It occurs along the whole Chilean coast, from southern Peru to southern Argentina [1]. The World Register of Marine Species (WoRMS) accepts it as a marine species; its only distribution record is New Zealand, and its sources include a list of rocky-intertidal invertebrates of Lima department [7].

The cyprid larvae, about 0.9 mm, settle on a wide range of submerged surfaces. In trials from October 2009 to July 2010 they settled on polyethylene tubes, plates and tarred fabric hung at depths of 4 to 6 m, at three Chilean sites between 29° and 41° south latitude [1].

An analysis of mitochondrial COI sequences along much of the Chilean coast found genetic structure among sites, stronger when populations were split north and south of 33° S; the authors attribute it to oceanographic transitions that affect species with pelagic larvae [5].

Outside its native range, a single joined group of specimens was collected in Port Wellington, New Zealand, and is reported among the first known introductions of the genus [4].

Biology

It is a simultaneous hermaphrodite: each individual has testes and an ovary and passes sperm to another through a penis. The testes are grouped in branching acini and two sperm ducts merge before reaching the penis, while the ovary is a sac surrounding the body. In September the ovaries were yellowish and held ovigerous lamellae with fertilised oocytes, embryos at several stages and free nauplii in the body cavity; in October they were whitish, thick-walled and filled with a milky fluid [2].

High fecundity and early sexual maturity are attributed to it. The main breeding period falls in spring and summer, and competent larvae are collected seasonally: from late spring to early summer, with a second period in autumn [1].

On collectors suspended in Metri Bay (41°36' S), individuals that settled in spring 2006 reached the average commercial size, about 36 mm carino-rostral length, after 20 months, and the minimum selling size, 21 mm, after 7 months. Harvest was possible between 18 and 24 months, with a yield of 20 to 30 g per commercial-sized individual [1].

Ecology

It is a sessile, gregarious, omnivorous species that feeds on seston filtered from the water. Its gregarious habit causes no density-dependent effects on growth, and it tolerates environmental change well [1]. Juvenile collection on collectors was higher at North Totoralillo (29°29' S) than in Tongoy and Metri bays [1].

Under controlled conditions, the authors cite an earlier study with faster growth at 10 °C than at 16 °C, and at 4–6 m depth than at 1–2 m [1]. In northern Chile it occurs together with Megabalanus concinnus, and its size structure varies across its range [5].

Conservation

In Chile, annual extractions declined progressively, between 685 and 159 t per year over the 10 years before the 2009 data, which suggests, though it is unproven, overexploitation of natural populations; the authors add that there is no information on overexploitation. Small-scale extraction was not subject to specific regulation, and no bans or restrictions had been imposed [1].

The period of greatest risk is spring and summer, when specimens that brood the whole embryonic development up to the first larva are removed; for that reason culture is also proposed as a way to repopulate natural beds [1].

Human relevance

In Chile it is a traditional resource of local small-scale fishing, aimed at the national market [1].

An assessment of culture in southern Chile estimated that one long-line can produce 7 to 10 t gross over the culture cycle and that producing frozen meat for the Japanese market would give a net present value of 490000 dollars, an internal rate of return of 32% and a payback of 4 years [1].

Its calcite shell has also been studied: the authors propose that its rough surface reflects crystallisation from an amorphous precursor [3].

References (7)

  1. López, D.A., López, B.A., Arriagada, S.E. et al. (2012). Diversification of Chilean aquaculture: the case of the giant barnacle Austromegabalanus psittacus (Molina, 1782). Latin American Journal of Aquatic Research, 596-607. doi:10.3856/vol40-issue3-fulltext-9 (accessed 2026-10-25)
  2. Contreras, C., Luna, N., Dupré, E. (2017). Reproductive system morphology of giant barnacle “picoroco” Austromegabalanus psittacus (Molina, 1782) (Cirripedia, Balanidae). Latin American Journal of Aquatic Research, 607-615. doi:10.3856/vol43-issue3-fulltext-24 (accessed 2026-10-25)
  3. Checa, A.G., Macías-Sánchez, E., Rodríguez-Navarro, A.B. et al. (2020). Origin of the biphase nature and surface roughness of biogenic calcite secreted by the giant barnacle Austromegabalanus psittacus. Scientific Reports. doi:10.1038/s41598-020-73804-8 (accessed 2026-10-25)
  4. Hosie, A., Ahyong, S.T. (2008). First records of the giant barnacles, Austromegabalanus nigrescens (Lamarck, 1818) and A. psittacus (Molina, 1782) (Cirripedia: Balanidae) from New Zealand, with a key to New Zealand Balanidae. Zootaxa, 59-64. doi:10.11646/zootaxa.1674.1.5 (accessed 2026-10-25)
  5. Pappalardo, P., Pitombo, F.B., Wares, J.P. et al. (2016). A rose by any other name: systematics and diversity in the Chilean giant barnacle Austromegabalanus psittacus (Molina, 1782) (Cirripedia). Journal of Crustacean Biology, 180-188. doi:10.1163/1937240x-00002403 (accessed 2026-10-25)
  6. Perreault, R.T. (2016). On the authorship of Austromegabalanus psittacus (Molina). Zootaxa. doi:10.11646/zootaxa.4169.2.7 (accessed 2026-10-25)
  7. WoRMS Editorial Board (2026). Austromegabalanus psittacus (Molina, 1788). World Register of Marine Species. https://www.marinespecies.org/aphia.php?p=taxdetails&id=535006 (accessed 2026-10-25)

Text: CC BY 4.0 · ORKA · version 1, published 3 Nov 2026.

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How to cite

ORKA (2026). Giant barnacle (Austromegabalanus psittacus). Marine life guide of Peru, species account version 1, published 2026-11-03. CC BY 4.0. https://guia.orkadive.com/en/species/austromegabalanus-psittacus

More pictures

  • Giant barnacle
    Photo: nebrooks · CC BY 4.0 · GBIF (iNaturalist research-grade observations)
  • Giant barnacle
    Photo: Eric Schmidt · CC BY 4.0 · GBIF (iNaturalist research-grade observations)

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