Published October 21, 2021 | Version v1
Taxonomic treatment Open

Pegantha martagon Haeckel 1879

  • 1. Muséum d'histoire naturelle, C. P. 6434, CH- 1211 Genève 6, Switzerland
  • 2. 880 NE 33 rd Street, Boca Raton, Florida, USA

Description

Pegantha martagon Haeckel, 1879

Fig. 53 A-C

Pegantha martagon Haeckel, 1879: 332.

Polycalpa zonaria Haeckel, 1879: 327, Mediterranean.

? Pegantha simplex Bigelow, 1904: 260, pl. 5 figs 19-20. – Bigelow, 1909: 83.‒ Bigelow, 1918: 395, synonym of P. martagon.

Pegantha martagon. ‒ Mayer, 1910: 443, figs 295-296. – Bigelow, 1909: 83, pl. 18 figs 1-8. ‒ Bigelow, 1918: 396. ‒ Kramp, 1955a: 160. ‒ Kramp, 1957: 67, pl. 6 fig. 1, revision. ‒ Kramp, 1959a: 64, 197, fig. 302. ‒ Kramp, 1961: 274. ‒ Kramp, 1968: 127, fig. 342. ‒ Segura-Puertas, 1984: 45, pl. 14 fig. 1. ‒ Pagès et al., 1992: 41, fig. 49. – Larson et al., 1989: 789, fig. 1A.

Examined material: BFLA4070; 1 specimen; 11-APR- 2019; size 10 mm, 10 tentacles; preserved in alcohol for DNA extraction; 16S sequence MW528666. – BFLA4109; 1 specimen; 03-JUN-2019; size 8 mm, 8 tentacles; part preserved in formalin and deposited as UF-013796, small part in alcohol for DNA extraction; 16S sequence MW528676. – BFLA4336; 1 specimen; 07-FEB-2020; size 6 mm, 9 tentacles; preserved in alcohol for DNA extraction; 16S sequence MW528708. – 26-FEB-2018; 1 specimen photographed, not collected, 9 tentacles.

Observations: Medusae hemispherical or slightly wider than high, diameter 6-10 mm, 8-10 tentacles and marginal lappets (Fig. 53A, C, E), stomach wide, up to 2/3 of bell diameter, no gastric jelly cone (Fig. 53B, E), without manubrial pockets, peripheral canals originating below tentacles (Fig. 53C), first descending parallel along the peronial fold, then along lappet periphery, rather thin (1/6 of lappet width), width constant. Marginal lappets rectangular to rounded, with 4-5 otoporpae (Fig. 53B), these short, max. twice the size of the width of the peripheral canals. Statocysts near otoporpae, about as many as otoporpae. Tentacles curved, tapering, held at approximately 45° upwards, proximal end pointed and horizontal; below tentacles a slight furrow in the exumbrella with the peronium (Fig. 53A).

16S Data: The three obtained haplotypes have only low sequence divergences (Table 1, Fig. 48), but there was no significant relationship to a sequence of P. martagon from the Eastern Pacific (GenBank MG979374, Fig. 48).

Distribution: Widely distributed in the tropical and subtropical parts of the Atlantic and Indo-Pacific Ocean (Bigelow, 1909; Kramp, 1959a; Bouillon, 1978c; Bleeker & Van der Spoel, 1988; Navas-Pereira & Vannuci, 1991; Bouillon & Barnett, 1999; Segura Puerta et al., 2003, 2009; Oliveira et al., 2016), surprisingly also in the cold waters around South Georgia and in Antarctic waters (Kramp, 1959a; Toda et al., 2008). Occurs in shallow waters, occasionally from 100 to 300 m depth (Kramp, 1957). Type locality: China Sea.

Remarks: Our samples had apparently not yet developed gonads, being thus not fully mature. The observed tentacle numbers of 8-10 were lower than the 16 given in Kramp (1959a, 1968), but this is a maximal number and most animals have actually only 10-13 tentacles and lappets (Bigelow, 1909; Kramp, 1957, 1959a). According to Bigelow (1909) and Kramp (1959a: 64), the final tentacle number (10-11) is attained early in development, though during further growth some few tentacles and lappets may occasionally be added.

Kramp (1957) observed that the lateral portions of peripheral canal in the lappets are broader than the transverse portions along the bell margin. This was not seen in the present material (Fig. 53 C-E).

Pegantha simplex Bigelow, 1904 – a nominal species based on a type specimen from the Maldive Islands – was later synonymized with Pegantha martagon by Bigelow himself (Bigelow, 1909, 1918). We think that Bigelow’s specimen from the Maldives nevertheless deviates quite strongly from the scope of P. martagon as described by later authors (see synonymy above). It was a small (3 mm) medusa but with fully developed, pendant-saclike gonads. It had 8 tentacles/lappets and reportedly 25 statocysts per lappet, more than twice the number usually seen in P. martagon. Later, Bigelow (1909) reexamined this material and had to revise this number. The contraction of the alcohol preserved material feigned the presence of more statocysts. Actually, also Haeckel (1879) in his first description reported 13-15 statocysts per lappet. Because he also had preserved material, Bigelow (1909) assumed that he was likewise mistaken. The gonads of P. martagon are variably described as a simple ring at the periphery of the stomach, or as irregularly lobed, pendant sacs. While it is possible that these two stages are only different developmental stages, we nevertheless suspect that the wide variation of the current concept of P. martagon indicates that it comprises several species. Our 16S sequences are very different from a tentatively identified P. martagon from California found parasitizing a planktonic polychaete Tomopteris (Bentlage et al., 2018).

Notes

Published as part of Schuchert, Peter & Collins, Richard, 2021, Hydromedusae observed during night dives in the Gulf Stream, pp. 237-356 in Revue suisse de Zoologie 128 (2) on pages 322-324, DOI: 10.35929/RSZ.0049, http://zenodo.org/record/5639938

Files

Files (5.6 kB)

Name Size Download all
md5:67ecab032412d18af2094c2d7166c988
5.6 kB Download

System files (47.4 kB)

Name Size Download all
md5:8dd175b9e7b5d1aa7b8d069494e40e21
47.4 kB Download

Linked records

Additional details

Biodiversity

Collection code
BFLA
Event date
2018-02-26 , 2019-04-11 , 2019-06-03 , 2020-02-07
Family
Solmarisidae
Genus
Pegantha
Kingdom
Animalia
Material sample ID
BFLA4070 , BFLA4109, UF-013796 , BFLA4336
Order
Narcomedusae
Phylum
Cnidaria
Scientific name authorship
Haeckel
Species
martagon
Taxon rank
species
Verbatim event date
2018-02-26 , 2019-04-11 , 2019-06-03 , 2020-02-07
Taxonomic concept label
Pegantha martagon Haeckel, 1879 sec. Schuchert & Collins, 2021

References

  • Haeckel E. 1879. Das System der Medusen. Erster Teil einer Monographie der Medusen. Denkschriften der Medicinisch- Naturwissenschaftlichen Gesellschaft zu Jena 1: I-XX, 1 - 360, 20 pls.
  • Bigelow H. B. 1904. Medusae from the Maldive Islands. Bulletin of the Museum of Comparative Zoology at Harvard College 39 (9): 245 - 269, pls 1 - 17.
  • Bigelow H. B. 1909. The Medusae. Reports on the scientific results of the expedition to the eastern tropical Pacific, in charge of Alexander Agassiz, by the U. S. Fish Commission steamer " Albatross " from October, 1904, to March, 1905. XVI. Memoirs of the Museum of comparative Zoology at Harvard College 37: 1 - 243, pls 1 - 48.
  • Bigelow H. B. 1918. Some Medusae and Siphonophora from the western Atlantic. Bulletin of the Museum of comparative Zoology of Harvard College 62: 363 - 442, pls 1 - 8.
  • Mayer A. G. 1910. Medusae of the world. Hydromedusae, Vols. I & II. Scyphomedusae, Vol III. Carnegie Institution, Washington, pp. 735, plates 1 - 76.
  • Kramp P. L. 1955 a. A revision of Ernst Haeckel's determinations of a collection of Medusae belonging to the Zoological Museum of Copenhagen. Deep Sea Research 3: 149 - 168.
  • Kramp P. L. 1957. Hydromedusae from the Discovery collections. Discovery Reports 29: 1 - 128.
  • Kramp P. L. 1959 a. The Hydromedusae of the Atlantic Ocean and adjacent waters. Dana Report 46: 1 - 283.
  • Kramp P. L. 1961. Synopsis of the medusae of the world. Journal of the Marine Biological Association of the U. K. 40: 1 - 469.
  • Kramp P. L. 1968. The hydromedusae of the Pacific and Indian oceans. Sections II and III. Dana Report 72: 1 - 200.
  • Segura-Puertas L. 1984. Morfologia, sistematica y zoogeografia de las medusas (Cnidaria, Hydrozoa y Scyphozoa) del Pacifico Tropical Oriental. Instituto de Ciencias del Mar y Limnologia, Universidad Nacional Autonoma de Mexico, Publicacion Especial 8: 1 - 320.
  • Pages F., Gili J. M., Bouillon J. 1992. Medusae (Hydrozoa, Scyphozoa, Cubozoa) of the Benguela Current (southeastern Atlantic). Scientia Marina 56 (Suppl. 1): 1 - 64.
  • Larson R. J., Mills C. E., Harbison G. R. 1989. In situ foraging and feeding behaviour of Narcomedusae (Cnidaria: Hydrozoa). Journal of the Marine Biological Association of the U. K. 69: 785 - 794.
  • Bouillon J. 1978 c. Hydromeduses de la mer de Bismarck (Papouasie, Nouvelle-Guinee). II. Limnomedusa, Narcomedusa, Trachymedusa et Laingiomedusa (sous classe nouv.). Cahiers de Biologie Marine 19: 473 - 483.
  • Van Der Spoel S., Bleeker J. 1988. Medusae from the Banda Sea and Aru Sea plankton, collected during the Snellius II expeditions, 1984 - 1985. Indo Malayan Zoology 5: 161 - 202.
  • Bouillon J., Barnett T. J. 1999. The marine fauna of New Zealand: Hydromedusae (Cnidaria: Hydrozoa). Niwa Biodiversity Memoir 113: 1 - 136.
  • Oliveira O. M. P., et al .. 2016. Census of Cnidaria (Medusozoa) and Ctenophora from South American marine waters. Zootaxa 4194 (1): 1 - 256. DOI: 10.11646 / zootaxa. 4194.1.1
  • Toda R., Lindsay D. J., Fuentes V. L., Moteki M. 2008. Community structure of pelagic cnidarians off Adelie Land, East Antarctica, during austral summer 2008. Polar Biology 37 (2): 269 - 289.
  • Bentlage B., Osborn K. J., Lindsay D. J., Hopcroft R. R., Raskoff K. A., Collins A. G. 2018. Loss of metagenesis and evolution of a parasitic life style in a group of open-ocean jellyfish. Molecular Phylogenetics and Evolution 124: 50 - 59.