Petrosia ficiformis

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Petrosia ficiformis
Petrosia ficiformis.jpg
Petrosia ficiformis is a purple brown sponge of the Mediterranean and North Atlantic
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Porifera
Class: Demospongiae
Order: Haplosclerida
Family: Petrosiidae
Genus: Petrosia
Species:
P. ficiformis
Binomial name
Petrosia ficiformis
(Poiret, 1879)
Synonyms [1]
List
  • Alcyonium distortum Lamarck, 1815
  • Petrosia dura (Schmidt, 1862)
  • Petrosia ficiformis (Poiret, 1789)
  • Rayneria dura Nardo, 1834
  • Reniera compacta Schmidt, 1864
  • Reniera dura Schmidt, 1862
  • Schmidtia dura (Schmidt, 1862)
  • Schmidtia ficiformis (Poiret, 1789)
  • Schmidtia fungiformis Balsamo Crivelli, 1863
  • Spongia ficiformis Poiret, 1789

Petrosia ficiformis, commonly known as the stony sponge, is a species of petrosiid sea sponge in the order Haplosclerida. [1]

Contents

Taxonomy

Petrosia ficiformis was first described by J.L.M. Poiret as Spongia ficiformers. Its name comes from the Greek: "pétra" - πέτρα - rock, "physis" - φύση - nature, "fórma" - φόρμα - shape, meaning "naturally-shaped rock". It is classified under the subgenus Petrosia of the genus Petrosia . [1]

Distribution

Petrosia ficiformis occurs in the Mediterranean Sea and in the adjacent eastern Atlantic Ocean. [1] [2] It is found among rocks and in caves and rock crevasses, typically deeper than 5 m (16 ft). [3]

Characteristics

Petrosia ficiformis is usually purple brown in colour due to symbiosis with photosynthetic cyanobacteria, but can be white in the absence of light. It has a compact, hard texture, with spherical oscula irregularly spread over the surface.

Chemistry

Petrosia ficiformis biosynthesizes various acetylene derivatives. A characteristic example of this is petrosynol, [4] a polyacetylene of 30 atoms, which was isolated in 1987 from this animal. It likely helps to protect the sponge from bacterial and fungal infections. [5]

Chemical structure of petrosynol Petrosynol.svg
Chemical structure of petrosynol

Petrosia ficiformis is specifically known to synthesize various types of petroformynes, a class of polyhydroxylated polyacetylene fatty alcohols with cytotoxic activity. [6] [2] The skeleton of these toxins is formed by a hydrocarbon chain of 46 to 47 carbon atoms. [7]

Predators

Petrosia ficiformis is predated by the nudibranch Peltodoris atromaculata . [2] [3] This nudibranch is a specialist on Petrosia, along with the chemically similar Haliclona fulva . There is no evidence that the nudibranch uses the chemical compounds of these sponges in their own defense, as is known for many other nudibranchs. [2]

References

  1. 1 2 3 4 Van Soest RW, Boury-Esnault N, Hooper JN, Rützler K, de Voogd NJ, de Glasby BA, Hajdu E, Pisera AB, Manconi R, Schoenberg C, Janussen D, Tabachnick KR, Klautau M, Picton B, Kelly M, Vacelet J, eds. (2025). "Petrosia (Petrosia) ficiformis (Poiret, 1789)". World Porifera Database. World Register of Marine Species . Retrieved 10 April 2025.
  2. 1 2 3 4 Gemballa, Sven; Schermutzki, Franka (2004). "Cytotoxic haplosclerid sponges preferred: a field study on the diet of the dotted sea slug Peltodoris atromaculata (Doridoidea: Nudibranchia)". Marine Biology. 144 (6): 1213–1222. doi:10.1007/s00227-003-1279-1.
  3. 1 2 Palomares ML, Pauly D, eds. (2025). "Petrosia ficiformis" in SeaLifeBase. February 2025 version.
  4. Krebs, H. C. en Progress in the Chemistry of Organic Natural Products; Volume 49, Herz, W.,Grisebach, H., Kirby, G. W., Tamm, C. Ed. Springer-Verlag: Wien-New York, 1986; pg 151-319.
  5. Meglitsch, P.A.; Schram, F.R. Invertebrate Zoology; 3 Ed, Oxford University Press: New York; 1991; page 623.
  6. Cimino, G.; De Giulio, A.; De Rosa, S.; Di Marzo, V. (1989). "High molecular weight polyacetylenes from Petrosia ficiformis: Further structural analysis and biological activity". Tetrahedron Letters. 30 (27): 3563–3566. doi:10.1016/S0040-4039(00)99441-3.
  7. Férnandez-Trillo, 2004, PhD Dissertation, Universidad de Santiago de Compostela, Síntesis de Poliacetilenos de Origen Marino: Síntesis de Callyberinas A-C y (−)-Siphonodiol.