AnimaliaNot EvaluatedacceptedspeciesAccepted
Pseudaegina rhodina

Pseudaegina rhodina

(Haeckel, 1879) Yes

GBIF:190510808

0year

ABOUT

Descriptions(6)

Fig 51 A-G, Fig. 52 A-B
Schuchert, Peter, Collins, Richard (2021): Hydromedusae observed during night dives in the Gulf Stream. Revue suisse de Zoologie 128 (2): 237-356, DOI: 10.35929/RSZ.0049
Observations Form with 5 tentacles: Umbrella approximately hemispherical, 15 - 20 mm, jelly firm, apical mesoglea half the bell height, tentacles issue at about 2 / 3 of bell height, above tentacles a small bulge (Fig. 51 A- B). Velum broad (Fig. 51 A). Stomach about half the bell diameter, mounted on a rounded mesogleal cone of the same diameter reaching to level of bell margin (Fig. 51 A). Mouth rim can form temporary folds or even a tubular extension with terminal folds (Fig. 51 D-F). Five subdivided manubrial pockets (Fig. 51 C-D). Manubrial pockets broadly U-shaped, reaching from stomach rim to about half the distance to bell margin (Fig. 51 A), in middle a narrow septum which does not reach to the stomach level or level of tentacle origin (Fig. 51 C, smp). At bottom of left and right side of the pairs of pouches originates a broad peripheral canal, directed first along peronium towards the bell margin and then following the latter (Fig. 51 C). Five tentacles originating in upper half of medusa at about upper level of stomach, the proximal end embedded in an exumbrellar furrow, the tentacle roots rather short, entering the mesoglea, tapering, and curved towards oral (Fig. 51 B); tentacle length about 2 - 3 bell diameters, curved towards oral, nematocysts concentrated on upper side but also present on underside. Below tentacles a deep cleft in exumbrella reaching down to bell margin, its floor with a thickened epidermis containing nematocysts (= peronium, Fig. 51 C-G). 48 to ca. 68 statocysts. No otoporpae. Almost colourless, greenish or yellowish cast in daylight. Form with 4 tentacles: As above, but only four tentacles and four pairs of manubrial pouches, size 9 to 11 mm, 36 to 60 statocysts.
Schuchert, Peter, Collins, Richard (2021): Hydromedusae observed during night dives in the Gulf Stream. Revue suisse de Zoologie 128 (2): 237-356, DOI: 10.35929/RSZ.0049
Remarks: Haeckel’s type material of this species consisted in three specimens. Two of them had four tentacles and a size of 40 mm, one had five tentacles and measured 50 mm. He depicted a mature female with four tentacles. The statocyst numbers were given as two per manubrial hemi-pouch (16 - 20 in total). Kramp (1955 b, 1961) synonymized this species with the similar Aegina citrea Eschscholtz, 1829, an opinion already pondered by Mayer (1910). This view was upheld until Lindsay et al. (2017) revised Aegina citrea and split it into several species and belonging to separate families, this based on morphological and genetic differences. The main morphological difference to Aegina is the shape of the tentacle root. In Aegina they are curved towards aboral, in Pseudaegina they are curved towards oral. Our specimens with 5 tentacles matched the description of Lindsay et al. (2017) very well as they came from the same region. There are, however, some differences to Haeckel’s description. Our specimens were smaller (up to 20 mm) but all immature. The most obvious difference is the number of statocysts: Haeckel saw about 16 - 20, while we found regularly 60 - 68. The haplotype divergence in our sample was high (p-value up to 7.8 %) and in the maximum likelihood tree the samples split into two sub-clades (Fig. 48). This separation coincided with two morphotypes: the four- and five-tentacled form (see above). Unfortunately, we could get only one sequence of the four-tentacled form and due to the low number of samples, this distribution could also be due to mere contingency. The four-tentacled medusae were all smaller than those with five tentacles and it is nevertheless the possible that our material was composed of two sister-species. Because the original material of Haeckel included both four- and five-tentacled forms, it is not possible to use the tentacle number in the diagnosis of a new species without the designation of a lectotype (or a neotype as Haeckel’s material is likely lost). A population-genetic study at the type locality combined with the designation of a neotype is thus needed to resolve this taxonomic problem. Because of these unresolved issues and because our samples were monophyletic, we felt it premature to describe one of the clades as a new species. One particularity not mentioned in previous descriptions concerns the temporary folds of the mouth region (Fig. 51 D-F). One of the figures in Lindsay et al. (2017: fig. 12 C) also shows this ruffling of the mouth margin. In one of our animals the mouth was even drawn out to a tube ending in a flower-like, folded mouth region. The folds disappeared after fixation. It is thus unlikely that they can ever be seen in standard net-plankton samples.
Schuchert, Peter, Collins, Richard (2021): Hydromedusae observed during night dives in the Gulf Stream. Revue suisse de Zoologie 128 (2): 237-356, DOI: 10.35929/RSZ.0049
16 S data: In the maximum likelihood tree (Fig. 48), all five samples clustered in a lineage that was well separated from most other Narcomedusae. The clade had a distinct internal dichotomy with the single 4 - tentacled specimen being rather apart from the 5 - tentacled medusae (7.6 to 7.8 % base pair differences). The three haplotypes of the 5 - tentacled medusae were rather similar (0.18 - 0.36 % divergences, Table 1).
Schuchert, Peter, Collins, Richard (2021): Hydromedusae observed during night dives in the Gulf Stream. Revue suisse de Zoologie 128 (2): 237-356, DOI: 10.35929/RSZ.0049
Distribution: Tropical to subtropical Atlantic Ocean (Lindsay et al., 2017). Type locality: Canary Islands, Lanzarote.
Schuchert, Peter, Collins, Richard (2021): Hydromedusae observed during night dives in the Gulf Stream. Revue suisse de Zoologie 128 (2): 237-356, DOI: 10.35929/RSZ.0049
Examined material Specimens with 5 tentacles: BFLA 4015; 1 specimen; 17 - JAN- 2019; size 18 mm; part preserved in formalin and deposited as UF- 013441, small part in alcohol for DNA extraction; 16 S sequence MW 528658. – BFLA 4047; 1 specimen; 01 - APR- 2019; size 16 mm; part preserved in formalin and deposited as UF- 013451, small part in alcohol for DNA extraction; 16 S sequence MW 528659. – BFLA 4067; 1 specimen; 10 - APR- 2019; size 20 mm; part preserved in formalin and deposited as UF- 013778, small part in alcohol for DNA extraction; 16 S sequence identical to MW 528659. – BFLA 4322; 1 specimen; 24 - JAN- 2020; size 15 mm; part preserved in formalin and deposited as UF- 013887, small part in alcohol for DNA extraction; 16 S sequence MW 528707. – 13 - MAR- 2020; 1 specimen; 15 mm; not collected. Specimens with 4 tentacles: BFLA 4120; 1 specimen; 04 - JUN- 2019; size 9 mm; part preserved in formalin and deposited as UF- 013803, small part in alcohol for DNA extraction; 16 S sequence MW 528678. – BFLA 4134; 1 specimen; 15 - JUN- 2019; size 11 mm; part preserved in formalin and deposited as UF- 013809, small part in alcohol for DNA extraction; 16 S sequence not determinable. – BFLA 4118; 1 specimen; 04 - JUN- 2019; size 9 mm; part preserved in formalin and deposited as UF- 013809, small part in alcohol for DNA extraction, not examined.
Schuchert, Peter, Collins, Richard (2021): Hydromedusae observed during night dives in the Gulf Stream. Revue suisse de Zoologie 128 (2): 237-356, DOI: 10.35929/RSZ.0049

Export occurrence data

Darwin Core Archive (ZIP)

CLASSIFICATION

Taxonomic Classification Tree

MULTIMEDIA

Media Files(3)

Fig. 51. Pseudaegina rhodina with 5 tentacles. (A-C) BFLA4015, size 18 mm. (D) BFLA4047, size 16 mm. (E-F) BFLA4067, size 20 mm. (G) BFLA4322, size 15 mm. (A) Lateral view. (B) Higher magnification of tentacle root (rte, arrow), note inflection towards below (= oral). (C) Details of bell margin. (D) Aboral view, note the (temporary) folding of mouth margin. (E-F) Medusa which has recently fed and its stomach is full of prey. Note the particular, most likely transitory, formation of a mouth tube and folded mouth margin, shown at higher magnification in F. (G). Lateral view. Abbreviations: man – manubrium/ stomach covering conical jelly cone, mmp – distal margin of manubrial pouch, pca – peripheral canal, per – peronium, rte – tentacle root, smp – septum in middle of manubrial pouch, sta – statocyst.

Imageimage/png© Schuchert, Peter;Collins, RichardSchuchert, Peter;Collins, Richard

Fig. 52. Pseudaegina rhodina with 4 tentacles. (A) BFLA4134, size 9 mm, animal has semi-digested prey items in its gastric system including the peripheral canal system rendering it thus much more visible. (B) BFLA4120, bell size 9 mm, lateral view.

Imageimage/png© Schuchert, Peter;Collins, RichardSchuchert, Peter;Collins, Richard

Fig. 48. Maximum likelihood phylogenetic tree of Narcomedusae obtained with PhyML (GTR+G+I model) and based on about 600 bp positions of the mitochondrial 16S gene. Node-support values are bootstrap values of 100 pseudoreplicates (shown only if> 70%). Sequence labels start with the GenBank numbers (except for identical haplotypes) permitting the retrieval of more information. Some proveniences were obtained from Lindsay et al. (2017) or through personal communications. Red ODEHOV DUH QHZ VHTXHQFHV IURP WKLV VWXG\. &RORXUHG ER[HV LQGLFDWH IDPLO\ DI¿OLDWLRQV DFFRUGLQJ WR WKH FXUUHQWO\ XVHG V\VWHP. (") 'HQRWHV SRVVLEOH PLVLGHQWL¿FDWLRQV.

Imageimage/png© Schuchert, Peter;Collins, RichardSchuchert, Peter;Collins, Richard

IMAGES

Gallery(3)

See Gallery

Occurrences with images

Source Information

Hydromedusae observed during night dives in the Gulf Stream

checklist

This dataset contains the digitized treatments in Plazi based on the original journal article Schuchert, Peter, Collins, Richard (2021): Hydromedusae observed during night dives in the Gulf Stream. Revue suisse de Zoologie 128 (2): 237-356, DOI: 10.35929/RSZ.0049

Abstract: Hydromedusae were photographed and collected during 75 night-time dives in the Gulfstream off Florida. Most of the collected material was used to obtain DNA extracts and subsequently to determine part of the mitochondrial 16S rRNA gene, a barcode marker preferentially used for hydrozoans. The morphological data and the 16S barcodes permitted us to identify 46 species and 6 additional species nameable only to the genus level. Photos and descriptions are provided for all of them and the taxonomy and species status discussed. Six new species are described: Pandeopsis prolifera n. spec., Zanclea mayeri n. spec., Corymorpha floridana n. spec., Staurodiscus luteus n. spec., Octophialucium irregularis n. spec., Solmaris flavofinis n. spec. The new family Wuvulidae is proposed for the genus Wuvula Bouillon, Seghers & Boero, 1988. The new name Aequorea neocyanea is introduced for Zygodactyla cyanea L. Agassiz, 1862 to avoid a secondary homonymy with Aequorea cyanea de Blainville, 1834. Zygodactyla cyanea was considered to be a synonym of Aequorea forskalea Péron & Lesueur, 1810 for most of the 20th century, but we present arguments that it should be kept distinct from the latter and it must be transferred to the genus Aequorea. The genus Otoporpa Xu & Zhang, 1978 is regarded here as congeneric with Pegantha Haeckel, 1879 and its type species Otoporpa polystriata Xu & Zhang, 1978 is therefore changed to Pegantha polystriata (Xu & Zhang, 1978) new comb. Dipleurosoma brooksii Mayer, 1910 is recognized as a new synonym of Staurodiscus kellneri (Mayer, 1910); Staurodiscus heterosceles Haeckel, 1879 as a new synonym of Staurodiscus tetrastaurus Haeckel, 1879; Orchistoma agariciforme Keller, 1884 and Tetracannota collapsum Mayer, 1900 both as new synonyms of Orchistoma pileus (Lesson, 1843). The following Indo-Pacific species are newly recorded for the Atlantic Ocean: Pandeopsis ikarii (Uchida, 1927), Aequorea taiwanensis Zheng et al., 2009; Zygocanna apapillatus Xu, Huang & Guo, 2014; Gastroblasta timida Keller, 1883; Cunina becki Bouillon, 1985; and Pegantha polystriata (Xu & Zhang, 1978). The 16S sequences also permitted us to discover several new links with polyp stages, this for Cirrhitiara superba (Mayer, 1900), Euphysilla pyramidata Kramp, 1955, Zancleopsis dichotoma, and Melicertissa mayeri Kramp, 1959. Detailed, high resolution photos of living medusae were found to be very useful for taxonomic purposes and are mostly preferable to preserved, damaged specimens obtained with plankton nets. Photos of living animals also permit us to better document material used to determine 16S barcodes and make the latter useable for taxonomic revisions.

Schuchert P, Collins R, felipe (2021). Hydromedusae observed during night dives in the Gulf Stream. Plazi.org taxonomic treatments database. Checklist dataset https://doi.org/10.35929/rsz.0049 accessed via GBIF.org on 2026-06-16.

CC0Published 10/21/2021View dataset
GBIF Usage Key
190510808
Dataset Key
172fa5c5-c0c4-4bd7-b710-d608237b8458
Origin
source
Backbone Key
9484726
Taxon ID
D0118A7C5B5F0042FC52F8C9FD327ED8.taxon
Last Crawled
6/9/2026
Last Interpreted
6/9/2026