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Journal articles on the topic 'Scyphozoa – Behavior'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Archdale, M. V. "Feeding Behavior in Scyphozoa, Crustacea and Cephalopoda." Chemical Senses 30, Supplement 1 (2005): i303—i304. http://dx.doi.org/10.1093/chemse/bjh235.

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2

Jarms, Gerhard, André Carrara Morandini, and Fábio Lang da Silveira. "Polyps of the families Atorellidae and Nausithoidae (Scyphozoa: Coronatae) new to the brazilian fauna." Biota Neotropica 2, no. 1 (2002): 1–11. http://dx.doi.org/10.1590/s1676-06032002000100004.

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Solitary scyphistomae of the scyphozoan order Coronatae were sorted from samples collected at 12 oceanographic stations of the Revizee-Score Sul/Bentos project along the Brazilian coast. The 201 specimens were found, at depths between 133-808 m, growing on stony corals. These scyphistomae were assigned to the families Nausithoidae (186) and Atorellidae (15) based on the outer morphology of the periderm tubes. The number and shape of the cusps, and the presence of second order teeth in some of them, suggests that the polyps should be split into four types, two of them assigned to Nausithoe Köll

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3

Tronolone, Valquiria Baddini, André Carrara Morandini, and Alvaro Esteves Migotto. "On the occurrence of scyphozoan ephyrae (Cnidaria, Scyphozoa, Semaeostomeae and Rhizostomeae) in the southeastern Brazilian coast." Biota Neotropica 2, no. 2 (2002): 1–18. http://dx.doi.org/10.1590/s1676-06032002000200008.

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The occurrence of ephyrae of the scyphozoan orders Semaeostomeae and Rhizostomeae is reported for the first time for the Brazilian coast. The specimens, caught in plankton tows in the São Sebastião Channel and the Cananéia lagoon estuarine system, are: Chrysaora lactea (Semaeostomeae), Phyllorhiza punctata (Rhizostomeae), and an unidentified species of Pelagia (Semaeostomeae). A table with all species of scyphozoan with the known life cycle is provided.

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4

GERSHWIN, LISA-ANN, and WOLFGANG ZEIDLER. "Two new jellyfishes (Cnidaria: Scyphozoa) from tropical Australian waters." Zootaxa 1764, no. 1 (2008): 41. http://dx.doi.org/10.11646/zootaxa.1764.1.4.

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Two new species of scyphozoan jellyfishes from tropical Australian waters are described. The first, Sanderia pampinosus, n. sp., from waters off northern Western Australia, represents the first record of the genus from Australia. It differs from its only other congener, S. malayensis Goette, 1886, in having: (1) almost double the number of gonadal papillae at about half the body size; (2) horseshoe-shaped gonadal rings; and (3) eradial tentacles that are flattened in the oral-aboral direction and have nematocyst clusters on all sides. The second species, Netrostoma nuda, n. sp., from the Great

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5

Pourjomeh, Fatemeh, Mohammad Reza Shokri, Hassan Rajabi-Maham, Hamid Rezai, and Elham Maghsoudlou. "New records of the scyphozoan medusae (Cnidaria: Scyphozoa) in the north of Gulf of Oman, Iran." Marine Biodiversity 48, no. 4 (2017): 2193–202. http://dx.doi.org/10.1007/s12526-017-0683-6.

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6

Migotto, Alvaro E., Antonio C. Marques, André C. Morandini, and Fábio L. da Silveira. "Checklist of the Cnidaria Medusozoa of Brazil." Biota Neotropica 2, no. 1 (2002): 1–31. http://dx.doi.org/10.1590/s1676-06032002000100010.

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Literature records were reviewed to compile a list of species of the marine taxa of Cnidaria Medusozoa recorded for the Brazilian coast. The total number of species of medusozoans so far recorded for Brazil is 373: 347 Hydrozoa, 3 Cubozoa: 23 Scyphozoa.

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7

Gómez Daglio, Liza, and Michael N. Dawson. "Species richness of jellyfishes (Scyphozoa : Discomedusae) in the Tropical Eastern Pacific: missed taxa, molecules, and morphology match in a biodiversity hotspot." Invertebrate Systematics 31, no. 5 (2017): 635. http://dx.doi.org/10.1071/is16055.

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Species richness in the seas has been underestimated due to the combined challenges presented by the taxonomic impediment, delimitation of species, preponderance of cryptic species, and uneven sampling effort. The mismatch between actual and estimated diversity varies by region and by taxon, leaving open questions such as: are hotspots for well-known taxa also hotspots for poorly known taxa? We address these challenges and this question for shallow-water scyphozoan jellyfishes in the Tropical Eastern Pacific (TEP). We increased sampling effort at 34 coastal locations along the TEP, and combine

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8

Passano, L. M. "Spasm behavior and the diffuse nerve-net in Cassiopea xamachana (Scyphozoa: Coelenterata)." Hydrobiologia 530-531, no. 1-3 (2004): 91–96. http://dx.doi.org/10.1007/s10750-004-3113-2.

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9

Schiariti, A., AC Morandini, G. Jarms, R. von Glehn Paes, S. Franke, and H. Mianzan. "Asexual reproduction strategies and blooming potential in Scyphozoa." Marine Ecology Progress Series 510 (September 9, 2014): 241–53. http://dx.doi.org/10.3354/meps10798.

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10

Herring, P. J., and E. A. Widder. "Bioluminescence of deep-sea coronate medusae (Cnidaria: Scyphozoa)." Marine Biology 146, no. 1 (2004): 39–51. http://dx.doi.org/10.1007/s00227-004-1430-7.

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11

Eggers, Norman, and Gerhard Jarms. "The morphogenesis of ephyra in Coronatae (Cnidaria, Scyphozoa)." Marine Biology 152, no. 3 (2007): 495–502. http://dx.doi.org/10.1007/s00227-007-0719-8.

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12

Zavodnik, D. "Spatial aggregations of the swarming jellyfish Pelagia noctiluca (Scyphozoa)." Marine Biology 94, no. 2 (1987): 265–69. http://dx.doi.org/10.1007/bf00392939.

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13

Schiariti, A., M. Kawahara, S. Uye, and H. W. Mianzan. "Life cycle of the jellyfish Lychnorhiza lucerna (Scyphozoa: Rhizostomeae)." Marine Biology 156, no. 1 (2008): 1–12. http://dx.doi.org/10.1007/s00227-008-1050-8.

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14

Brown, Michael K., and Mark J. Gibbons. "Null models for null hypotheses in taxonomy: a test using Scyphozoa." Biological Journal of the Linnean Society 134, no. 1 (2021): 240–45. http://dx.doi.org/10.1093/biolinnean/blab070.

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Abstract Although molecular tools are becoming more important in the delineation of scyphozoan species there is, perforce, a need to substantiate new species definitions using morphological data. Access to type material is often difficult and detailed, raw morphometric data are rarely provided in older type descriptions, which makes comparisons of new with old challenging. Here, we use null models based on simple measures of central tendency to generate morphometric data sets for four species of Aurelia, three species of Chrysaora and two species of Crambionella. The results of PERMANOVA and C

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15

Turk, Valentina, Davor Lučić, Vesna Flander-Putrle, and Alenka Malej. "Feeding ofAureliasp. (Scyphozoa) and links to the microbial food web." Marine Ecology 29, no. 4 (2008): 495–505. http://dx.doi.org/10.1111/j.1439-0485.2008.00250.x.

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16

Martellos, Stefano, Luca Ukosich, and Massimo Avian. "JellyWeb: an interactive information system on Scyphozoa, Cubozoa and Staurozoa." ZooKeys 554 (January 18, 2016): 1–25. http://dx.doi.org/10.3897/zookeys.554.6745.

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17

Chapman, David M. "Microanatomy of the bell rim of Aurelia aurita (Cnidaria: Scyphozoa)." Canadian Journal of Zoology 77, no. 1 (1999): 34–46. http://dx.doi.org/10.1139/z98-193.

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The bell rim of Aurelia aurita is described in detail. This medusa has usually eight marginal sensory complexes and many tentacle chambers, the latter made up of a roof, sides (lappets), and a floor. The sole contents of a tentacle chamber are a few bladelike tentacle bases. The distal tentacle is narrow and moniliform and grooved on the adoral side with a folded sheet of muscle fibers on the deep side. Between the underside of the tentacle chamber's floor and a more adoral circumferential flange (pseudovelarium) lies a ciliated food groove lined with a thick amuscular epithelium containing or

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18

Marino, A., R. Crupi, G. Musci, and G. La Spada. "Morphological integrity and toxicological properties ofPelagia noctiluca (Scyphozoa) nematocysts." Chemistry and Ecology 22, sup1 (2006): S127—S131. http://dx.doi.org/10.1080/02757540600677757.

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19

Diupotex-Chong, Maria Esther, Alberto Ocaña-Luna, and Marina Sánchez-Ramírez. "Chromosome analysis ofAurelia auritaLinné, 1758 (Scyphozoa: Ulmaridae), southern Gulf of Mexico." Marine Biology Research 5, no. 4 (2009): 399–403. http://dx.doi.org/10.1080/17451000802534907.

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20

Uriz, M.-J., D. Rosell, and M. Maldonado. "Parasitism, commensalism or mutualism? The case of Scyphozoa (Coronatae) and horny sponges." Marine Ecology Progress Series 81 (1992): 247–55. http://dx.doi.org/10.3354/meps081247.

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21

Barz, Kristina, Hans-Harald Hinrichsen, and Hans-Jürgen Hirche. "Scyphozoa in the Bornholm Basin (central Baltic Sea)–The role of advection." Journal of Marine Systems 60, no. 1-2 (2006): 167–76. http://dx.doi.org/10.1016/j.jmarsys.2006.01.002.

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22

Sandrini, L. Rottini, and M. Avian. "Feeding mechanism of Pelagia noctiluca (Scyphozoa: Semaeostomeae); laboratory and open sea observations." Marine Biology 102, no. 1 (1989): 49–55. http://dx.doi.org/10.1007/bf00391322.

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23

G., Jarms, Tiemann H., and Båmstedt U. "Development and biology of Periphylla periphylla (Scyphozoa: Coronatae) in a Norwegian fjord." Marine Biology 141, no. 4 (2002): 647–57. http://dx.doi.org/10.1007/s00227-002-0858-x.

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24

Toshino, Sho. "New record of Linuche draco (Scyphozoa, Coronatae, Linuchidae) from Japan." Plankton and Benthos Research 15, no. 4 (2020): 327–33. http://dx.doi.org/10.3800/pbr.15.327.

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25

Albert, David J. "Aurelia labiata medusae (Scyphozoa) in Roscoe Bay avoid tidal dispersion by vertical migration." Journal of Sea Research 57, no. 4 (2007): 281–87. http://dx.doi.org/10.1016/j.seares.2006.11.002.

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26

Sötje, Ilka, and Gerhard Jarms. "Derivation of the reduced life cycle of Thecoscyphus zibrowii Werner, 1984 (Cnidaria, Scyphozoa)." Marine Biology 156, no. 11 (2009): 2331–41. http://dx.doi.org/10.1007/s00227-009-1261-7.

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27

Pitt, K. A. "Life history and settlement preferences of the edible jellyfish Catostylus mosaicus (Scyphozoa: Rhizostomeae)." Marine Biology 136, no. 2 (2000): 269–79. http://dx.doi.org/10.1007/s002270050685.

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28

Dawson, M. N. "Macro-morphological variation among cryptic species of the moon jellyfish, Aurelia (Cnidaria: Scyphozoa)." Marine Biology 143, no. 2 (2003): 369–79. http://dx.doi.org/10.1007/s00227-003-1070-3.

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29

Dawson, M. N. "Macro-morphological variation among cryptic species of the moon jellyfish, Aurelia (Cnidaria: Scyphozoa)." Marine Biology 144, no. 1 (2004): 203. http://dx.doi.org/10.1007/s00227-003-1230-5.

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30

Hofmann, D. K., and T. G. Honegger. "Bud formation and metamorphosis inCassiopea andromeda (Cnidaria: Scyphozoa): A developmental and ultrastructural study." Marine Biology 105, no. 3 (1990): 509–18. http://dx.doi.org/10.1007/bf01316322.

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31

Strand, S. W., and W. M. Hamner. "Predatory behavior ofPhacellophora camtschatica and size-selective predation uponAurelia aurita (Scyphozoa: Cnidaria) in Saanich Inlet, British Columbia." Marine Biology 99, no. 3 (1988): 409–14. http://dx.doi.org/10.1007/bf02112134.

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32

DE MORAES LEME, JULIANA, MARCELLO GUIMARÃES SIMÕES, ANTONIO CARLOS MARQUES, and HEYO VAN ITEN. "CLADISTIC ANALYSIS OF THE SUBORDER CONULARIINA MILLER AND GURLEY, 1896 (CNIDARIA, SCYPHOZOA; VENDIAN–TRIASSIC)." Palaeontology 51, no. 3 (2008): 649–62. http://dx.doi.org/10.1111/j.1475-4983.2008.00775.x.

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33

Hedwig, Von Monika, and W. Schäfer. "Vergleichende Untersuchungen zur Ultrastruktur and zur phylogenetischen Bedeutung der Spermien der Scyphozoa." Journal of Zoological Systematics and Evolutionary Research 24, no. 2 (2009): 109–22. http://dx.doi.org/10.1111/j.1439-0469.1986.tb00619.x.

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34

Morandini, André Carrara, and Gerhard Jarms. "New combinations for two coronate polyp species (Atorellidae and Nausithoidae, Coronatae, Scyphozoa, Cnidaria)." Contributions to Zoology 74, no. 1-2 (2005): 117–23. http://dx.doi.org/10.1163/18759866-0740102008.

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Within the order Coronatae, six valid species remain known only by their polyp stage. The inability to relate them to any medusae genera of the group is a problem that remains to be solved in the order. With the examination of type specimens, we reassign the species Stephanoscyphistoma sibogae and S. striatus to the genera Atorella and Nausithoe respectively.

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35

Gershwin, Lisa-Ann, and Allen G. Collins. "A preliminary phylogeny of Pelagiidae (Cnidaria, Scyphozoa), with new observations of Chrysaora colorata comb. nov." Journal of Natural History 36, no. 2 (2002): 127–48. http://dx.doi.org/10.1080/00222930010003819.

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36

Holst, Sabine, and Gerhard Jarms. "Responses of solitary and colonial coronate polyps (Cnidaria, Scyphozoa, Coronatae) to sedimentation and burial." Journal of Experimental Marine Biology and Ecology 329, no. 2 (2006): 230–38. http://dx.doi.org/10.1016/j.jembe.2005.09.014.

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37

STRAEHLER-POHL, ILKA, CHAD L. WIDMER, and ANDRÉ C. MORANDINI. "Characterizations of juvenile stages of some semaeostome Scyphozoa (Cnidaria), with recognition of a new family (Phacellophoridae)." Zootaxa 2741, no. 1 (2011): 1. http://dx.doi.org/10.11646/zootaxa.2741.1.1.

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Phacellophora camtschatica has long been assigned to the semaeostome scyphozoan family Ulmaridae. Early stages (scyphistomae, strobilae, ephyrae, postephyrae, and young medusae) of the species were compared with those of several other semaeostomes currently assigned to Ulmaridae, Pelagiidae, and Cyaneidae. Juveniles of P. camtschatica did not strictly conform with characters of those of any of these families, and appeared intermediate between Cyaneidae and Ulmaridae. A new family, Phacellophoridae, is proposed to accommodate P. camtschatica.

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38

Hansson, LJ. "Effect of temperature on growth rate of Aurelia aurita (Cnidaria, Scyphozoa) from Gullmarsfjorden, Sweden." Marine Ecology Progress Series 161 (1997): 145–53. http://dx.doi.org/10.3354/meps161145.

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39

N Dawson, Michael, and William M. Hamner. "Geographic variation and behavioral evolution in marine plankton: the case of Mastigias (Scyphozoa, Rhizostomeae)." Marine Biology 143, no. 6 (2003): 1161–74. http://dx.doi.org/10.1007/s00227-003-1155-z.

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40

Chapman, David M. "Development of the tentacles and food groove in the jellyfish Aurelia aurita (Cnidaria: Scyphozoa)." Canadian Journal of Zoology 79, no. 4 (2001): 623–32. http://dx.doi.org/10.1139/z01-016.

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The development of the tentacle-bearing part of the rim of the jellyfish Aurelia aurita is described. The newly liberated ephyra lacks appendages at the bell rim between the rhopalial arms (null stage). The next stage (bump stage) has a subumbrellar bump near the rim. The bump then forms a tongue process (tongue stage) on its adoral side. The aboral part of the bump becomes the primordium of the tentacle. The tongue process elongates and spreads circumferentially, finally melding with the lappets of the rhopalial arms. Next the tongue process develops a groove that spreads laterally. The epith

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41

Ben Faleh, AR, H. Allaya, A. Armani, and AAB Shahin. "Significant genetic differentiation among meroplanktonic barrel jellyfish Rhizostoma pulmo (Cnidaria: Scyphozoa) in the Mediterranean Sea." African Journal of Marine Science 39, no. 1 (2017): 1–8. http://dx.doi.org/10.2989/1814232x.2017.1303395.

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42

Leoni, Valentina, Delphine Bonnet, Eduardo Ramírez‐Romero, and Juan Carlos Molinero. "Biogeography and phenology of the jellyfish Rhizostoma pulmo (Cnidaria: Scyphozoa) in southern European seas." Global Ecology and Biogeography 30, no. 3 (2021): 622–39. http://dx.doi.org/10.1111/geb.13241.

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43

Dawson, Michael N. "Incipient speciation of Catostylus mosaicus (Scyphozoa, Rhizostomeae, Catostylidae), comparative phylogeography and biogeography in south-east Australia." Journal of Biogeography 32, no. 3 (2005): 515–33. http://dx.doi.org/10.1111/j.1365-2699.2004.01193.x.

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44

Kawahara, M., SI Uye, K. Ohtsu, and H. Iizumi. "Unusual population explosion of the giant jellyfish Nemopilema nomurai (Scyphozoa: Rhizostomeae) in East Asian waters." Marine Ecology Progress Series 307 (January 24, 2006): 161–73. http://dx.doi.org/10.3354/meps307161.

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45

Stopar, Katja, Andreja Ramšak, Peter Trontelj, and Alenka Malej. "Lack of genetic structure in the jellyfish Pelagia noctiluca (Cnidaria: Scyphozoa: Semaeostomeae) across European seas." Molecular Phylogenetics and Evolution 57, no. 1 (2010): 417–28. http://dx.doi.org/10.1016/j.ympev.2010.07.004.

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46

Swift, H. F., L. Gómez Daglio, and M. N. Dawson. "Three routes to crypsis: Stasis, convergence, and parallelism in the Mastigias species complex (Scyphozoa, Rhizostomeae)." Molecular Phylogenetics and Evolution 99 (June 2016): 103–15. http://dx.doi.org/10.1016/j.ympev.2016.02.013.

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47

Sötje, Ilka, Henry Tiemann, and Ulf Båmstedt. "Trophic ecology and the related functional morphology of the deepwater medusa Periphylla periphylla (Scyphozoa, Coronata)." Marine Biology 150, no. 3 (2006): 329–43. http://dx.doi.org/10.1007/s00227-006-0369-2.

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48

Ohtsu, Kohzoh, Masato Kawahara, Hideki Ikeda, and Shin-ichi Uye. "Experimental induction of gonadal maturation and spawning in the giant jellyfish Nemopilema nomurai (Scyphozoa: Rhizostomeae)." Marine Biology 152, no. 3 (2007): 667–76. http://dx.doi.org/10.1007/s00227-007-0722-0.

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49

ZEIDLER, WOLFGANG, JACOB DOUEK, BARUCH RINKEVICH, ROY GEVILI, MENACHEM GOREN, and BELLA S. GALIL. "Validation and redescription of the hyperiidean amphipod Brachyscelus rapacoides Stephensen, 1925 (Crustacea: Amphipoda: Hyperiidea: Brachyscelidae), a new record of association with the scyphozoan jellyfish Rhopilema nomadica Galil, 1990 (Scyphozoa: Rhizostomeae: Rhizostomatidae) in the Mediterranean Sea." Zootaxa 4471, no. 3 (2018): 523. http://dx.doi.org/10.11646/zootaxa.4471.3.5.

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The hyperiidean amphipod Brachyscelus rapacoides Stephensen, 1925 is recorded from the scyphozoan jellyfish Rhopilema nomadica Galil, 1990, a new record of association for the genus Brachyscelus, as well as the first record of hyperiid infestation of a non-indigenous scyphozoan host. Because of some past confusion concerning the status of B. rapacoides and the closely related species B. rapax (Claus, 1871) a redescription of B. rapacoides and molecular analysis are provided in order to validate it as a species distinguished from B. rapax.

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50

Ben Faleh, AR, A. Ben Othmen, T. Deli, A. Annabi, and K. Said. "High genetic homogeneity of the moon jellyAurelia aurita(Scyphozoa, Semaeostomeae) along the Mediterranean coast of Tunisia." African Journal of Marine Science 31, no. 1 (2009): 73–80. http://dx.doi.org/10.2989/ajms.2009.31.1.6.777.

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