Olindias deigo

From Species-ID
Jump to: navigation, search
Notice: This page is derived from the original publication listed below, whose author(s) should always be credited. Further contributors may edit and improve the content of this page and, consequently, need to be credited as well (see page history). Any assessment of factual correctness requires a careful review of the original article as well as of subsequent contributions.

If you are uncertain whether your planned contribution is correct or not, we suggest that you use the associated discussion page instead of editing the page directly.

This page should be cited as follows (rationale):
Toshino S, Tanimoto M, Minemizu R (2019) Olindias deigo sp. nov., a new species (Hydrozoa, Trachylinae, Limnomedusae) from the Ryukyu Archipelago, southern Japan. ZooKeys 900 : 1–21, doi. Versioned wiki page: 2019-12-31, version 181549, https://species-id.net/w/index.php?title=Olindias_deigo&oldid=181549 , contributors (alphabetical order): Pensoft Publishers.

Citation formats to copy and paste

BibTeX:

@article{Toshino2019ZooKeys900,
author = {Toshino, Sho AND Tanimoto, Miyako AND Minemizu, Ryo},
journal = {ZooKeys},
publisher = {Pensoft Publishers},
title = {Olindias deigo sp. nov., a new species (Hydrozoa, Trachylinae, Limnomedusae) from the Ryukyu Archipelago, southern Japan},
year = {2019},
volume = {900},
issue = {},
pages = {1--21},
doi = {10.3897/zookeys.900.38850},
url = {https://zookeys.pensoft.net/articles.php?id=38850},
note = {Versioned wiki page: 2019-12-31, version 181549, https://species-id.net/w/index.php?title=Olindias_deigo&oldid=181549 , contributors (alphabetical order): Pensoft Publishers.}

}

RIS/ Endnote:

TY - JOUR
T1 - Olindias deigo sp. nov., a new species (Hydrozoa, Trachylinae, Limnomedusae) from the Ryukyu Archipelago, southern Japan
A1 - Toshino S
A1 - Tanimoto M
A1 - Minemizu R
Y1 - 2019
JF - ZooKeys
JA -
VL - 900
IS -
UR - http://dx.doi.org/10.3897/zookeys.900.38850
SP - 1
EP - 21
PB - Pensoft Publishers
M1 - Versioned wiki page: 2019-12-31, version 181549, https://species-id.net/w/index.php?title=Olindias_deigo&oldid=181549 , contributors (alphabetical order): Pensoft Publishers.

M3 - doi:10.3897/zookeys.900.38850

Wikipedia/ Citizendium:

<ref name="Toshino2019ZooKeys900">{{Citation
| author = Toshino S, Tanimoto M, Minemizu R
| title = Olindias deigo sp. nov., a new species (Hydrozoa, Trachylinae, Limnomedusae) from the Ryukyu Archipelago, southern Japan
| journal = ZooKeys
| year = 2019
| volume = 900
| issue =
| pages = 1--21
| pmid =
| publisher = Pensoft Publishers
| doi = 10.3897/zookeys.900.38850
| url = https://zookeys.pensoft.net/articles.php?id=38850
| pmc =
| accessdate = 2024-12-23

}} Versioned wiki page: 2019-12-31, version 181549, https://species-id.net/w/index.php?title=Olindias_deigo&oldid=181549 , contributors (alphabetical order): Pensoft Publishers.</ref>

See also the citation download page at the journal.


Taxonavigation

Ordo: Limnomedusae
Familia: Olindiidae
Genus: Olindias

Name

Olindias deigo Toshino & Tanimoto & Minemizu, 2019 sp. nov.Wikispecies linkZooBank linkPensoft Profile

New Japanese name

Deigo-hanagasa-kurage.

Material examined

Holotype: NSMT-Co1690. Ada, Kunigami, Okinawa Prefecture, Ryukyu Archipelago, southern Japan; 26°43'29.0"N, 128°19'7.0"E; March 11, 2018; collector: Shuhei Odoriba. Paratypes: NSMT-Co1691. Same locality as holotype, March 16, 2018, collector: Shuhei Odoriba. NSMT-Co1692. Motobu, Okinawa Prefecture, Ryukyu Archipelago, southern Japan; 26°40'18.0"N, 127°52'49.0"E; April 19, 2015; collector: Shinichi Arakawa.

Description

Mature medusae with transparent, dome-like exumbrella (Figs 3A, 4A). Umbrella height about 40 mm and umbrella diameter about 80 mm (Table 2). Exumbrella smooth, lacking nematocyst warts (Fig. 3B). Four radial canals elongate from four corners of stomach (Figs 3B, C, 4B). Folded gonads attached along entire length of four radial canals (Fig. 5A). Immature gonads light red to orange (Figs 3D, 4C) while mature gonads are milky-white in color. Manubrium long, length about 50% of umbrella height, with quadrate base, light red to orange in color, folded (Fig. 5B, C). Mouth quadrate to rhomboid (Fig. 5C). Oral rips complexly folded (Fig. 5C). White fibrous structures scattered in mesoglea of exumbrella (Fig. 5D). Different length of black bands elongated from umbrella margin to the apex of exumbrella (Fig. 5F). Centripetal canals about 80 to 100, long and short alternately aligned (Fig. 5D). Long canals reached apex of the umbrella while short ones were half or quarter length that of long canals terminating in tentacles. Some canals connected or branched (Fig. 5D). Tentacles and marginal clubs aligned on the umbrella margin (Figs 3D, 5E). Primary tentacles about 80 to 140, thin, short with distal adhesive pads and cnidocysts in transverse clasps. Color of exumbrella tentacles and primary tentacles pale black with purple and glowing green tips and with black base (Fig. 3D). Number of secondary tentacles about 50, thick, no adhesive pads, cnidocysts in rings, deep-brown in color (Fig. 3D). Contracted secondary tentacle short, coil-like while elongate ones reaching 2 m in length. Exumbrella tentacles about 30 to 60, developing on tip of black bands (Fig. 5F). Shape and color similar to those of primary tentacles (Fig. 3D). Number of marginal clubs about 170 to 240, rounded, short, whitish in color (Fig. 3D). Statocysts were not found in fixed mature medusae.

Table 2. Size (mm) of Olindias deigo sp. nov. *: the holotype. Nos. Co1691-1692 are paratypes. **: damaged. CC = centripetal canal; ET = exumbrella tentacle; PT = primary tentacle; MC = Marginal club; ST = secondary tentacle; UD = umbrella width; UH = umbrella height.
Specimen No. UH (mm) UD (mm) No. of ET No. of CC No. of PT No. of ST No. of MC Sampling site Date Lat./ long.
NSMT-Co1690* 39.5 67.1 33 83 112 51 238 Ada, Kunigami, Okinawa 11/03/2018 26°43'29.0"N, 128°19'7.0"E
NSMT-Co1691 44.7 83.7 66 104 141 (29)** 242 Ada, Kunigami, Okinawa 16/03/2018 26°43'29.0"N, 128°19'7.0"E
NSMT-Co1692 29.9 61.8 30 86 78 49 168 Motobu, Okinawa 19/04/2015 26°40'18.0"N, 127°52'49.0"E

Life cycle

Fertilization and polyp formation. Spawning occurred in dark conditions. Thousands of fertilized eggs were collected from the bottom of the tank in the early morning (from 8 to 9 am); diameter of blastocysts ~100 µm (Fig. 6A). Blastocysts developed into planulae within two days. Planulae had a pear-shaped body, 70 µm in diameter and 130 µm in length (Fig. 6B); they developed into polyps within 20 days.
The polyps form small colonies by elongation of the stolon, developing into a network (Fig. 6C–F). The hydrorhizae were cylindrical with small egg-shaped or cylindrical hydranths developing on the stolon. The hydranths had an ovoid body, 0.7 mm in length (Fig. 6E). The body was divided in two parts, gastric region (0.3 mm in diameter and 0.5 mm in length) and hypostome (0.2 mm in diameter and 0.2 mm in length). Tentacle single, filiform, 1.7 mm in length (Fig. 6E, F). The hydroid, usually brownish or yellowish, became orange or pink owing to the consumption of Artemia nauplii. Tentacle and hypostome transparent. Budding and development of young medusa. Budding of young medusae was observed after 8 months of polyp formation. Medusa bud formation occurred on stolon (Fig. 7A) at temperatures below 20 °C. The shape of the buds was ovoid and 0.3 mm in diameter (Fig. 7A). Two days after onset of budding, four radial canals and a circular canal appeared, but were obscure (Fig. 7B). Eight days after onset of budding, rudiments of tentacles developed from the bud (Fig. 7C). Fourteen days after onset of budding, the buds enlarged (0.8 mm in diameter) and green fluorescence was observed on the tentacles (Fig. 7D). Fifteen days after onset of budding, the medusa buds detached.
Newly detached medusae had a spherical umbrella translucent in color (Fig. 8A–C). Umbrella height about 1.6 mm and diameter about 1.5 mm. Exumbrella with tiny nematocysts along entire exumbrella (Fig. 8D). Four simple radial canals from four corners of the stomach (Fig. 8B, D). Statocysts four, enclosed in mesoglea, adjacent to primary tentacles (Fig. 8E). Manubrium long, about 50% that of umbrella height (Fig. 8F). Marginal tentacles of two types (Fig. 8C, G, H). Primary tentacles four, short (about 1 to 2 times that of umbrella diameter) bearing nematocyst clusters on the tips (Fig. 8G). Secondary tentacles two, long (about 5 times that of umbrella diameter) bearing 10 to 20 nematocyst batteries (Fig. 8H). The medusae attached using the tip of the primary tentacles, but adhesive pad was not observed (Fig. 8G). Green fluorescence was observed at the base of tentacles and four corners of the stomach (Fig. 8D–F).
Ninety-day-old medusae were about 10 mm in diameter (Fig. 9A). Umbrella bowl-shaped. Primary and secondary tentacles about 40 and 20, respectively. About 20 centripetal canals were observed. Medusae aged 120-day-old were about 15 mm in diameter (Fig. 9B). White fibrous structures appeared around radial canals. Manubrium elongated and mouth rips developed. Number of primary and secondary tentacles and radial canals not increased much. Medusae aged 150-day-old were about 20 mm in diameter (Fig. 9C). Primary and secondary tentacles about 60 and 20, respectively. About 20 centripetal canals observed. Exumbrella tentacles developed near umbrella margin, but were not observed on the apex of exumbrella. Medusae aged 200-day-old were about 40 mm in diameter (Fig. 9D). Primary and secondary tentacles about 80 and 40, respectively. About 60 centripetal canals were observed. Gonad developed. Exumbrella tentacles developed near the margin of umbrella and the middle part of exumbrella. Medusae aged 240-day-old were about 60 mm in diameter (Fig. 9E). Primary and secondary tentacles about 120 and 40, respectively. About 60 centripetal canals observed. Gonad developed and matured. Spawning observed (Fig. 9E). Cnidome. Two different nematocyst types were identified and measured in the adult medusae, young medusae, and mature polyps (Table 3). Adult medusae had two nematocyst types. Two sizes of macrobasic b-mastigophores (Fig. 10A, B) and microbasic euryteles (Fig. 10C, D) were found on primary, secondary, and exumbrella tentacles. Young medusae had two nematocyst types. Macrobasic b-mastigophores (Fig. 10E, F) were found only on tentacles while two sizes of microbasic euryteles (Fig. 10G–J) were found on primary, secondary, and exumbrella tentacles. The mature polyps had one nematocyst type, microbasic euryteles (Fig. 10K, L).

Table 3. Cnidomes of Olindias deigo sp. nov. D, L represent capsule diameter and length, respectively, in μm.
Stage Part Type Min Max Mean SD N
Adult medusae Primary tentacle Macrobasic p-mastigophore (Large) D 5.69 8.75 7.37 0.63 50
L 34.19 42.44 38.95 1.99 50
Macrobasic p-mastigophore (Small) D 3.24 5.15 4.02 0.45 50
L 13.01 18.58 16.48 1.18 50
Microbasic eurytele D 8.01 10.91 9.84 0.77 50
L 20.56 28.48 24.61 1.94 50
Young medusae Exumbrella Microbasic eurytele (Large) D 5.66 8.32 7.10 0.72 14
L 13.70 20.02 17.62 1.78 14
Microbasic eurytele (Small) D 2.09 4.68 3.40 0.49 28
L 6.39 10.47 8.64 1.07 28
Tentacle Macrobasic p-mastigophore D 6.04 7.85 6.77 0.46 50
L 26.29 34.62 30.42 2.25 50
Microbasic eurytele (Large) D 6.33 9.49 7.70 0.68 44
L 15.70 23.62 20.04 2.35 44
Microbasic eurytele (Small) D 2.62 4.33 3.53 0.43 50
L 6.82 11.97 9.37 1.03 50
Hydroids Body Microbasic eurytele D 4.01 8.31 5.59 0.72 100
L 9.29 16.95 12.62 1.50 100
Tentacle Microbasic eurytele D 3.79 7.35 5.93 0.72 94
L 10.75 16.61 13.05 1.20 94

Molecular phylogenetics

In the resulting maximum likelihood tree (Fig. 11), four major monophyletic clades were formed in the genus Olindias: 1) O. formosus; 2) Olindias muelleri Haeckel, 1879; 3) O. sambaquiensis; 4) Olindias tenuis (Fewkes, 1882); and 5) a fifth group (O. deigo). The monophyly of O. deigo was evident in the 16S phylogenetic tree with high bootstrap values (99%), strongly supporting the validity of the new species. The Kimura 2-parameter distance between O. deigo and O. formosus was 0.03, below the distance 0.06–0.11 between olindiids (Table 4). Interspecific distance 0.000–0.002 between O. formosus from Iwate Prefecture, eastern Japan and O. formosus from Oita and Miyazaki prefectures, western Japan. Therefore, K2P divergence factor between 0.03–0.11 could be a threshold for discriminating olindiid species.

Table 4. Pairwise genetic distances (K2P) based on 410 positions of 16S sequences among Limnomedusae. The analysis involved 27 sequences.
No. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26
1 Aglauropsis aeora EU293973
2 Astrohydra japonica EU293975 0.226
3 Craspedacusta sinensis AY512507 0.230 0.220
4 Craspedacusta sowerbyi EU293971 0.258 0.197 0.089
5 Craspedacusta ziguiensis EU293974 0.220 0.194 0.051 0.073
6 Gonionemus sp. KF962480 0.178 0.236 0.229 0.247 0.210
7 Gonionemus vertens EU293976 0.187 0.246 0.239 0.253 0.216 0.030
8 Gonionemus vertens KX656923 0.178 0.233 0.226 0.243 0.206 0.002 0.027
9 Maeotias marginata AY512508 0.145 0.203 0.175 0.183 0.151 0.154 0.160 0.154
10 Scolionema suvaense AB720909 0.201 0.243 0.213 0.233 0.191 0.133 0.130 0.130 0.169
11 Olindias deigo LC508961 0.198 0.263 0.237 0.240 0.213 0.207 0.200 0.203 0.188 0.178
12 Olindias deigo LC508962 0.201 0.263 0.237 0.237 0.207 0.207 0.200 0.203 0.188 0.178 0.005
13 Olindias deigo LC508963 0.204 0.263 0.233 0.233 0.204 0.203 0.197 0.200 0.184 0.175 0.007 0.002
14 Olindias deigo LC508964 0.204 0.267 0.240 0.240 0.210 0.210 0.197 0.207 0.191 0.181 0.007 0.002 0.005
15 Olindias formosus LC508965 0.188 0.253 0.230 0.237 0.204 0.200 0.187 0.197 0.169 0.181 0.027 0.027 0.025 0.030
16 Olindias formosus LC508966 0.188 0.253 0.230 0.237 0.204 0.200 0.187 0.197 0.169 0.181 0.027 0.027 0.025 0.030 0.000
17 Olindias formosus LC508967 0.188 0.253 0.230 0.237 0.204 0.200 0.187 0.197 0.169 0.181 0.027 0.027 0.025 0.030 0.000 0.000
18 Olindias formosus LC508968 0.189 0.254 0.230 0.237 0.204 0.201 0.188 0.197 0.169 0.182 0.028 0.028 0.025 0.030 0.000 0.000 0.000
19 Olindias formosus LC508969 0.189 0.254 0.230 0.237 0.204 0.201 0.188 0.197 0.169 0.182 0.028 0.028 0.025 0.030 0.000 0.000 0.000 0.000
20 Olindias formosus LC508970 0.188 0.253 0.233 0.240 0.207 0.200 0.187 0.197 0.169 0.181 0.030 0.030 0.027 0.033 0.002 0.002 0.002 0.002 0.002
21 Olindias formosus KF184031 0.188 0.253 0.230 0.237 0.204 0.200 0.187 0.197 0.169 0.181 0.027 0.027 0.025 0.030 0.000 0.000 0.000 0.000 0.000 0.002
22 Olindias mulleri AY512509 0.217 0.274 0.244 0.254 0.213 0.210 0.197 0.206 0.175 0.191 0.072 0.072 0.069 0.074 0.061 0.061 0.061 0.061 0.061 0.064 0.061
23 Olindias mulleri EU293978 0.217 0.274 0.244 0.254 0.213 0.210 0.197 0.206 0.175 0.191 0.072 0.072 0.069 0.074 0.061 0.061 0.061 0.061 0.061 0.064 0.061 0.000
24 Olindias sambaquiensis EU293977 0.214 0.260 0.253 0.257 0.226 0.220 0.216 0.220 0.197 0.204 0.094 0.096 0.094 0.099 0.088 0.088 0.088 0.088 0.088 0.088 0.088 0.066 0.066
25 Olindias sambaquiensis KT266630 0.218 0.263 0.257 0.260 0.229 0.216 0.213 0.216 0.194 0.200 0.096 0.099 0.096 0.102 0.091 0.091 0.091 0.091 0.091 0.091 0.091 0.064 0.064 0.002
26 Olindias tenuis MG979369 0.217 0.253 0.233 0.230 0.213 0.207 0.207 0.207 0.157 0.200 0.096 0.096 0.093 0.099 0.088 0.088 0.088 0.088 0.088 0.091 0.088 0.077 0.077 0.108 0.105
27 Monobrachium parasiticum EU293970 0.234 0.344 0.314 0.351 0.299 0.265 0.258 0.261 0.218 0.276 0.241 0.241 0.241 0.245 0.224 0.224 0.224 0.225 0.225 0.224 0.224 0.231 0.231 0.259 0.262 0.262

Habitat and ecology

Medusae of O. deigo appeared in shallow waters (from 3 to 10 m) during winter and spring in a range of subtropical temperature localities in the Ryukyu Archipelago, southern Japan. The medusae rested on the sandy bottom or in areas with a good slope and movement of water during the daytime while they drifted and swam by extending their tentacles during the night. Thus, the species seems to be nocturnal in behavior. Stinging events attributable to O. deigo have not been reported thus far.

Etymology

The species name comes from the beautiful appearance of the jellyfish. The Japanese name deigo (noun in apposition) means Erythrina variegata which is popular as the “prefectural flower” of Okinawa.

Differential diagnosis

A comparison of key features of the species in the genus Olindias is presented in Table 5. All species of Olindias have four radial canals and numerous centripetal canals; numerous tentacles of two kinds: primary ones issuing above the umbrella margin, with distal adhesive pads and cnidocysts in transverse clasps and secondary ones on the umbrella margin, no adhesive pads, cnidocyst in rings; gonads with papilliform processes, on radial canals; numerous marginal clubs, statocyst usually in pairs at base of primary tentacles (Bouillon et al. 2006[1]). Olindias deigo can be distinguished from other Olindiidae species by the number and color of tentacles in adult medusae. Many more primary tentacles than secondary tentacles in O. deigo, O. formosus, and O. singularis, while fewer primary tentacles than secondary tentacles in O. malayensis, O. muelleri, O. sambaquiensis, and O. tenuis (Table 5). Several exumbrella tentacles present in O. deigo and O. formosus while lacking in others. Exumbrella tentacles of O. deigo many more than those of O. formosus (84 vs 30–60, respectively). The primary tentacles were colorful (black, purple, and glow green) in O. deigo and O. formosus, while they were red and yellow in O. malayensis, O. muelleri, O. sambaquiensis, and O. tenuis (no data for O. singularis and Olindias sp.) (Table 5).

Table 5. Morphology of adult medusae in previous and the present study. Bars represent a lack of data.
O. deigo sp. nov. O. formosus O. malayensis O. mulleri O. sambaquiensis O. singularis O. tenuis Olindias sp. (young medusa)
UD (mm) 62–84 83.2 75 25–35 40–60 22–44 50–100 13–36 35 7
UH (mm) 30–45 42.6 about 1/2 of UD over 1/2 of UD half of UD 5.5
No. of ET 30–60 84 present absent absent absent absent absent absent absent
No. of PT 78–141 168 264 20–30 50–60 48–60 80–100 28–86 32–54 12
No. of ST 49–51 57 325 30–40 100–120 96–120 200–300 16–50 38–70
No. of MC 168–242 283 120 100–170 100–200 32 to more than 100 64–69
No. of CC (per quadrant) 20–26 19–23 18–23 7–9 11–19 7–11 21–27 4–12 7–10 1
No. of gonads 4 4–6 4–6 4 4 4 4 4 4 4
Gonads Folded/ along nearly whole length of radial canals Folded/ along nearly whole length of radial canals Papilliform/ along nearly whole length of radial canals Linear, swollen, with surfaces covered with branched processes/ over nearly entire length of radial canals Papilliform/along the radial canals Folded/ along nearly whole length of radial canals Papilliform/ outer half of radial canals Papilliform/ outer half of radial canals Folded/ upper half of the radial canals
Statocysts Not examined Not examined Twice as many as primary tentacles Twice as many as primary tentacles Twice as many as primary tentacles Twice as many as primary tentacles Single otolith at base of each primary tentacle Single otolith at base of each tentacle Two at the base of two centripetal canals
Color Manubrium light red to orange. Gonads milky-white. Primary tentacles pale black with purple and glowing green tips and black base. Secondary tentacles deep-brown. Manubrium lilac to red orange. Each corner of base of manubrium smaragdine-green. Gonads egg-yellow. Tips of primary and exumbrellar tentacles transparent, lilac and smaragdine-green. Marginal clubs and base of primary and exumbrella tentacles ivory-black. Radial canals and circular canals deep scarlet. Centripetal canals lighter scarlet. Similar to O. mulleri Similar to O. tenuis but apparently browner and duller. Gonads orange Bright and variable, with mingled yellow, red, brown, and black. Colors similar to O. tenuis. Entoderm of stomach, gonads, and ring-canal opaque (cream color?). Entoderm of manubrium, tentacle-bulbs, and gonads opaque yellowish-green, streaked with purple. Exumbrella tentacles white or dark-purple. Marginal tentacles red and yellow.
Distribution (Sampling locality) Ryukyu archipelagos, Okinawa, southern Japan Oita, Japan Japan; Korea Malay Archipelago Bahamas; Bermudas; Mediterranean Sea; West Africa Aegean Sea Brazil; Argentina Maldive Is.; Low Archipelago; Chagos Archipelago; Philippines; India Australia; Iranian Gulf; Pakistan Florida; Bahamas; Barmudas; Cuba Sunda Strait
References This study This study Goto (1903)[2] Kramp (1961)[3] Park (2006)[4] Maas (1905)[5] Mayer (1910)[6] Kramp (1961)[3] Mayer (1910)[6] Kramp (1961)[3] Aytan et al. (2019)[7] Müller (1861)[8] Mayer (1910)[6] Kramp (1961)[3] Chiaverano et al. (2004)[9] Browne (1905)[10] Mayer (1910)[6] Kramp (1961)[3] Fewkes (1883)[11] Maas (1905)[5] Mayer (1910)[6] Kramp (1961)[3] Uchida (1947)[12]

Original Description

  • Toshino, S; Tanimoto, M; Minemizu, R; 2019: Olindias deigo sp. nov., a new species (Hydrozoa, Trachylinae, Limnomedusae) from the Ryukyu Archipelago, southern Japan ZooKeys, 900: 1-21. doi

Images

Other References

  1. Bouillon J, Gravili C, Gili J, Boero F (2006) An introduction to Hydrozoa.Mémoires du Muséum National d’Histoire Naturelle194: 1–591.
  2. Goto S (1903) The craspedote medusa Olindias and some of its natural allies.Mark Anniversary1: 1–22. https://doi.org/10.5962/bhl.title.3959
  3. 3.0 3.1 3.2 3.3 3.4 3.5 Kramp P (1961) Synopsis of the medusae of the world.Journal of the Marine Biological Association of the United Kingdom40: 1–469. https://doi.org/10.1017/S0025315400007347
  4. Park J (2006) New Records of Some Hydromedusae (Cnidaria: Hydrozoa) in Korea.Animal Systematics, Evolution and Diversity22(2): 169–177.
  5. 5.0 5.1 Maas O (1905) Die craspedoten medusen der Siboga-expedition.Siboga Expeditie10: 1–84. https://doi.org/10.5962/bhl.title.11301
  6. 6.0 6.1 6.2 6.3 6.4 Mayer A (1910) Medusae of the world.Carnegie Institution of Washington109: 1–735. https://doi.org/10.5962/bhl.title.159245
  7. Aytan Ü, Aksu İ, Bektaş Y (2019) Recent occurrence of Olindias muelleri Haeckel, 1879 (Cnidaria, Hydrozoa, Limnomedusae, Olindiidae) in the Aegean Sea.Plankton and Benthos Research14(1): 22–28. https://doi.org/10.3800/pbr.14.22
  8. Müller O (1861) Polypen und quallen von Santa Catharina. Olindias sambaquiensis, n. sp.Archiv für Naturgeschichte27: 312–319.
  9. Chiaverano L, Mianzan H, Ramírez F (2004) Gonad development and somatic growth patterns of Olindias sambaquiensis (Limnomedusae, Olindiidae).Hydrobiologia530(1–3): 373–381. https://doi.org/10.1007/s10750-004-2666-4
  10. Browne E (1905) Report on the medusae (Hydromedusae, Scyphomedusae and Ctenophora) collected by Prof. Herdman at Ceylon in 1902.Report to the Government of Ceylon on Pearl Oyster Fisheries of the Gulf of Manaar4: 132–166.
  11. Fewkes J (1883) On a few medusae from the Bermudas, in Exploration of the surface fauna of the Gulf Stream, under the auspices of the United States Coast Survey, by Alexander Agassiz.Bulletin of the Museum of Comparative Zoology at Harvard University11(3): 79–90.
  12. Uchida T (1947) Some medusae from the Central Pacific. Journal of the Faculty of Science, Hokkaido (Imperial) University, ser.VI, Zoology7(3): 297–319.