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Sea stars, urchins and sea cucumbers · Arbaciidae

Arbacia nigra

Arbacia nigra (Molina, 1782)

IUCN status: Not evaluated
Peruvian Register of Marine Species
Listed in PeRMS (IMARPE)
Arbacia nigra
Photo: Erasmo Macaya Horta · CC BY 4.0 · Wikimedia Commons

Species account

Summary

Arbacia nigra is a regular rocky-shore sea urchin native to the Pacific coast of South America, from northern Peru to southern Chile [1]. It was described in 1782 as Echinus niger, was long known as Tetrapygus niger, and since 2023 has been placed in Arbacia as the sister species of Arbacia dufresnii [2],[3]. It is a herbivore that feeds mostly on brown algae and keeps mussels from colonising the rock [4],[5].

Etymology

Molina described the species in 1782 as Echinus niger [3]. Agassiz erected the genus Tetrapygus in 1841 for this single species, and in 1846 A. Agassiz had already proposed the combination Arbacia nigra [2]. Using mitochondrial (COI), nuclear (28S) and morphological data, Courville and colleagues returned the species to Arbacia in 2023, and the WoRMS record treats Tetrapygus niger as a superseded combination [2],[3].

Distribution and habitat

It lives along the Pacific coast of South America from northern Peru to southern Chile, on rock and artificial structures in rocky habitats, especially where there are kelp forests and strong wave action [1]. A review places its range from the low intertidal down to 10 m depth, with juveniles mainly in crevices shallower than 2.5 m [1].

In central Chile, the shallowest part of the subtidal and the shallow edge of the Lessonia trabeculata forest served as recruitment zones between March and November 1990, and juveniles under 24 mm test diameter were associated with crevices [6]. Outside the kelp bed the animals appeared aggregated, and abundance declined toward the centre of the kelp forest [6].

Biology

It is a generalist herbivore whose diet consists mostly of brown algae, plus algal turfs, encrusting coralline algae, drift algae, mussel recruits and crustaceans [1]. In the intertidal of central Chile, Lessonia spp. made up 68% of the diet, and gonad development depended on the availability of drift kelp [4]. In Ancón bay in Peru, gut-content and isotope analyses showed that it also eats benthic macroalgae [5].

The larva is an unusual form of echinopluteus which, in culture at 14–18 °C, spent 94 to 120 days in the plankton and grew to more than 4.5 mm [7]. Roughly 40% of the larvae became juveniles, and the whole change from feeding larva to feeding adult lasted 4 to 6 days [7]. In controlled cultures, early development depends on temperature: reaching the early blastula took 14 hours at 15 °C, 45 hours at 10 °C and 164 hours at 5 °C [8].

Ecology

In the low intertidal of Ancón bay, in central Peru, inclusion and exclusion experiments showed that this species prevents sessile organisms from colonising the substrate, including the dominant mussel Semimytilus algosus [5]. The authors suggest that by limiting mussels it may reduce the diversity of associated species, and that by keeping rock bare it benefits other grazers [5].

A review describes it as the most abundant urchin in Peru and Chile, with densities of up to 85 individuals per m2, and notes that at such densities barrens can form where algal growth is inhibited [1]. In Chile some individuals live on elevated surfaces and so avoid the predatory sea stars Heliaster helianthus and Meyenaster gelatinosus: in trials the urchin took 48% less time to break contact on elevated surfaces than on the bottom [9]. The experiments point to Meyenaster gelatinosus as a greater threat than Heliaster helianthus [9].

Health, toxicological and chemical relevance

Not medical advice. For a sting, a poisoning or an allergy, seek medical care.

Among 77 specimens from the central Peruvian coast, sampled at Pucusana, La Punta and Ventanilla, 905 microplastic-like particles were recovered, that is 11.75 per individual, mostly yellow, blue and red fragments and fibres [10]. In an earlier study of the species, the digestive tract held on average 3.22 microplastics per individual, with a range of 1 to 5, and fibres made up 75.9% [11].

At Caleta Horcón, an industrial zone in Chile, the gonads of urchins fed on algae cultivated there accumulated metals (Cu, As, Cd and Pb) at concentrations between 5 and 798 times higher than in the alga [12].

Human relevance

Embryos, larvae and sperm of this species have been used as laboratory material: one study used sperm nuclei to measure lipid peroxidation from oxidative stress with hydrogen peroxide [13], and another described embryonic development at 5, 10 and 15 °C [8]. Outside its native range, a 2007 record from an aquaculture facility in South Africa led to its listing as an introduced species, but a new survey in September 2014 found it at no site, and removal from invasive-species lists was recommended [1].

Where to see it in Peru

The Peruvian literature documents it in the rocky low intertidal of Ancón bay, at 11°46′S, where it lives alongside the snail Tegula atra [5]. A study published in 2026 gathered specimens at Pucusana, La Punta and Ventanilla, on the central littoral [10]. A review indicates that it occupies the low intertidal down to about 10 m depth, and that it is found particularly where there are kelp forests and strong wave action [1].

References (13)

  1. Mabin, C.A., Wilson, J.R.U., Robinson, T.B. (2015). The Chilean black urchin, Tetrapygus niger (Molina, 1782) in South Africa: gone but not forgotten. BioInvasions Records 4, 261-264. doi:10.3391/bir.2015.4.4.05 (accessed 2026-10-25)
  2. Courville, E., Poulin, E., Saucède, T. et al. (2023). Taxonomic reassessment of Tetrapygus niger (Arbacioida, Echinoidea): molecular and morphological evidence support its placement in Arbacia. Zootaxa, 249-261. doi:10.11646/zootaxa.5375.2.6 (accessed 2026-10-25)
  3. WoRMS Editorial Board (2026). Arbacia nigra (Molina, 1782). World Register of Marine Species. https://www.marinespecies.org/aphia.php?p=taxdetails&id=569287 (accessed 2026-10-25)
  4. Rodríguez, S.R. (2003). Consumption of drift kelp by intertidal populations of the sea urchin Tetrapygus niger on the central Chilean coast: possible consequences at different ecological levels. Marine Ecology Progress Series 251, 141-151. doi:10.3354/meps251141 (accessed 2026-10-25)
  5. Hidalgo, F.J., Firstater, F.N., Lomovasky, B.J. (2013). Grazing effects of the sea urchin Tetrapygus niger and the snail Tegula atra on a rocky shore of central Peru. Journal of the Marine Biological Association of the United Kingdom 93, 2059-2066. doi:10.1017/S0025315413000994 (accessed 2026-10-25)
  6. Rodriguez, S.R., Ojeda, F.P. (1993). Distribution patterns of Tetrapygus niger (Echinodermata: Echinoidea) off the central Chilean coast. Marine Ecology Progress Series 101, 157-162. doi:10.3354/meps101157 (accessed 2026-10-25)
  7. Fuentes, I., Barros, C. (2000). Larval development and metamorphosis of cultured Tetrapygus niger (Echinodermata Echinoidea): an uncommon form of echinoplutei. Invertebrate Reproduction & Development 37, 201-209. doi:10.1080/07924259.2000.9652420 (accessed 2026-10-25)
  8. Olaechea, P., Panéz, J.J., Gonzáles-Figueroa, H. (2017). Desarrollo embrionario de Tetrapygus niger (Molina, 1782) “erizo negro” en diferentes temperaturas. Biotempo 6, 27-31. doi:10.31381/biotempo.v6i0.879 (accessed 2026-10-25)
  9. Urriago, J.D., Himmelman, J.H., Gaymer, C.F. (2012). Sea urchin Tetrapygus niger distribution on elevated surfaces represents a strategy for avoiding predatory sea stars. Marine Ecology Progress Series 444, 85-95. doi:10.3354/meps09396 (accessed 2026-10-25)
  10. Iannacone Oliver, J.A., Obregón-Ruiz, V.A., Nuñez-Bolaños, F.A. (2026). Partículas tipo microplástico en el erizo negro Arbacia nigra (Molina, 1782) (Echinoidea: Arbaciidae) en tres playas de la costa central del Perú. Innovaciencia 14. doi:10.15649/2346075x.6414 (accessed 2026-10-25)
  11. De-la-Torre, G.E., Dioses-Salinas, D.C., Huamantupa-Aybar, S. (2020). Preliminary observations of plastic debris in the gastrointestinal tract of sea urchin Tetrapygus niger. Brazilian Journal of Natural Sciences 3. doi:10.31415/bjns.v3i2.94 (accessed 2026-10-25)
  12. Latorre-Padilla, N., Meynard, A., Rivas, J. (2021). Transfer of Pollutants from Macrocystis pyrifera to Tetrapygus niger in a Highly Impacted Coastal Zone of Chile. Toxics 9. doi:10.3390/toxics9100244 (accessed 2026-10-25)
  13. Huerta Canales, D., Oré Sifuentes, R., Núñez Fonseca, M. (2000). El "erizo de mar" Tetrapygus niger como marcador biológico de estrés oxidativo. Revista Peruana de Biología 7, 198-201. doi:10.15381/rpb.v7i2.6827 (accessed 2026-10-25)

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

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How to cite

ORKA (2026). Arbacia nigra. Marine life guide of Peru, species account version 1, published 2026-11-01. CC BY 4.0. https://guia.orkadive.com/en/species/arbacia-nigra

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More pictures

  • Arbacia nigra
    Photo: Cody Hinchliff · CC BY 4.0 · GBIF (iNaturalist research-grade observations)
  • Arbacia nigra
    Photo: Álvaro Parra Valdivia · CC BY 4.0 · GBIF (iNaturalist research-grade observations)

Where it has been recorded

Sea regions where it has been recorded: Arbacia nigraThe highlighted regions link to their species list and say why it is on it; those with a dotted outline say “no scientific records”: there are no open records of this species there and no curator has confirmed it there.Tropicalnorthern seaTropical–coldtransition zoneIsolated recordColdcentral seaWith recordsColdsouthern seaWith records
  • Filled: scientific records, or confirmed by a curator
  • Hatched: isolated record
  • Dotted outline: no scientific records and no curator's confirmation (an ORKA sighting is not drawn here)

From openly licensed OBIS and GBIF records (CC0 or CC BY). How each list is built.

Related species

From the same genus (Arbacia).

Names and sources

Learn more

Conservation status: no data (IUCN). Taxonomy: PeRMS / WoRMS (CC BY 4.0).