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Figure 5 in New taxa of Japanese and New Zealand Eurystomellidae (Phylum Bryozoa) and their phylogenetic relationships

Figure 5. The strict consensus of 39 final trees. Synapomorphies for each clade in the ingroups are indicated by solid bars: lunulitiform colony (1), encrusting colony (1¢), ancestrular attachment without cementation (2), subtatiform ancestrular frontal wall (3), gymnocystal foramina (6), lack of well-formed costae (8), zooid deeper than length (12), undifferentiated proximal corners of orificial anter (13), indented proximolateral corners of orificial poster (15), vestigial excavations in gymnocystal surface (16), small excavations in gymnocystal surface (16¢), lack of medial suture in proximal rim or orifice (18), maternal orifice slightly dimorphic (19), endozooidal brooding of embryos (20), two kenozooidal foramina (22), one central plus two small kenozooidal foramina (22¢), interzooidal communications with pore-chambers (25).

Figure 4 in New taxa of Japanese and New Zealand Eurystomellidae (Phylum Bryozoa) and their phylogenetic relationships

Figure 4. One of the 39 most parsimonious trees obtained from the final analysis carried out by PAUP*. The transformations of all 25 skeletal characters are mapped (cf. Character List).

Figure 3. A–C in New taxa of Japanese and New Zealand Eurystomellidae (Phylum Bryozoa) and their phylogenetic relationships

Figure 3. A–C, Integripeltra shirayamai sp. nov. Saiki-wan, Honshu. A, autozooids, x, 70. B, maternal zooids with foraminate kenozooids distally, ¥116. C, autozooidal orifice with proximal rim partly removed to show how the long crescentic slits are merely the frontal expressions of the proximolateral embayments of the orifice, ¥201. D, E, Integripelta umbonata sp. nov. NZOI Stn Z9697. F, autozooids and a maternal zooid with foraminate distal kenozooid, ¥106. G, prox-

Figure 2. A, B in New taxa of Japanese and New Zealand Eurystomellidae (Phylum Bryozoa) and their phylogenetic relationships

Figure 2. A, B. Integripelta novella sp. nov. Hokkaido, intertidal. A, autozooids and two maternal zooids, the kenozooid distal to the one at left lacking a foramen, ¥89. B, maternal zooid with distal foraminate kenozooid, ¥121. C, D, Integripelta japonica sp. nov. Mi-shimi, Honshu. C, autozooids and maternal zooids, ¥53. D, maternal orifice and kenozooid, ¥211. E, F, Integripelta sextaria sp. nov. NZOI Stn Z9700. E, autozooids and maternal zooids, ¥48. F, autozooidal orifice, ¥181.

Figure 1. A, B in New taxa of Japanese and New Zealand Eurystomellidae (Phylum Bryozoa) and their phylogenetic relationships

Figure 1. A, B, Eurystomella foraminigera. Greta Point, Wellington, intertidal. A, group of zooids, ¥65. B, suboral rim, showing triradiate suture, ¥803. C-E, Eurystomella biperforata sp. nov. C,E, NZOI Stn Z9700. C, group of autozooids, ¥53. D, NZOI Stn Z9677, maternal zooid with distal foraminate kenozooid, ¥95. E, rare zooid with a single foramen, ¥163. F, Eurystomella aupouria sp. nov. NZOI Stn Z9716, ¥63.

opencc-by-4.0Dec 2024View details →

Phylum Cnidaria (Hydrozoa) CANTATA Transcriptomes

CANTATA is a Community bAsed Non-bilaTeriAn Transcriptome Archive aiming to provide an archive of non-bilaterian transcriptomic resources assembled and annotated in a standardized manner. In this repository, we provide the transcriptomes assemblies corresponding to the Phylum Cnidaria (Class Hydrozoa). Currently, the following species are available:<ul><li>Aegina citrea</li><li>Apolemia lanosa</li><li>Bargmannia amoena</li><li>Bargmannia elongata</li><li>Bargmannia lata</li><li>Chelophyes appendiculata</li><li>Chuniphyes multidentata</li><li>Craseoa lathetica</li><li>Erenna richardi</li><li>Forskalia asymmetrica</li><li>Hippopodius hippopus</li><li>Hydractinia symbiolongicarpus</li><li>Hydra oligactis</li><li>Hydra viridissima K10</li><li>Hydra vulgaris AEP</li><li>Lilyopsis fluoracantha</li><li>Liriope tetraphylla</li><li>Lychnagalma utricularia</li><li>Marrus claudanielis</li><li>Millepora alcicornis</li><li>Nanomia bijuga</li><li>Physalia physalis</li><li>Resomia ornicephala</li><li>Rhizophysa filiformis</li><li>Stephalia dilata</li></ul>The details about the read files used to assemble each transcriptome can be found at the CANTATA repository (https://gitlab.lrz.de/palmuc/cantata)

opencc-by-4.0Nov 2023View details →

Phylum Ctenophora CANTATA Transcriptomes

CANTATA is a Community bAsed Non-bilaTeriAn Transcriptome Archive aiming to provide an archive of non-bilaterian transcriptomic resources assembled and annotated in a standardized manner. In this repository, we provide the transcriptomes assemblies corresponding to the Phylum Ctenophora. Currently the following species are available:<ul><li>Aulacoctena acuminata</li><li>Bathocyroe fosteri</li><li>Bathyctena chuni</li><li>Beroe abyssicola</li><li>Beroe forskalii</li><li>Beroe ovata</li><li>Bolinopsis microptera</li><li>Cestum veneris</li><li>Charistephane fugiens</li><li>Deiopea kaloktenota</li><li>Dryodora glandiformis</li><li>Euplokamis dunlapae</li><li>Haeckelia beehleri</li><li>Haeckelia rubra</li><li>Hormiphora californensis</li><li>Lampea lactea</li><li>Lampocteis cruentiventer</li><li>Leucothea pulchra</li><li>Ocyropsis maculata</li><li>Thalassocalyce inconstans</li><li>Velamen paralellum</li></ul>The details about the read files used to assemble each transcriptome can be found at the CANTATA repository (https://gitlab.lrz.de/palmuc/cantata)

opencc-by-4.0Aug 2024View details →

Phylum Porifera CANTATA Transcriptomes

CANTATA is a Community bAsed Non-bilaTeriAn Transcriptome Archive aiming to provide an archive of non-bilaterian transcriptomic resources assembled and annotated in a standardized manner. In this repository, we provide the transcriptomes assemblies corresponding to the Phylum Porifera. Currently the following species are available: Demospongiae: <ul> <li>Amphimedon queenslandica</li> <li>Aplysina aerophoba</li> <li>Axinella polypoides</li> <li>Baikalospongia bacillifera</li> <li>Chondrosia reniformis (ASG)</li> <li>Cinachyrella alloclada</li> <li>Cliona varians</li> <li>Crella elegans</li> <li>Cymbastella concentrica</li> <li>Dendrilla antarctica</li> <li>Dysidea avara</li> <li>Ephydatia fluviatilis</li> <li>Ephydatia muelleri</li> <li>Geodia atlantica</li> <li>Geodia hentscheli</li> <li>Geodia macandrewii</li> <li>Geodia phlegraei</li> <li>Halichondria panicea</li> <li>Haliclona amboinensis</li> <li>Haliclona tubifera</li> <li>Halisarca dujardinii</li> <li>Lantrunculia apicalis</li> <li>Lendenfeldia chondrodes</li> <li>Lubomirskia abietina</li> <li>Lubomirskia baikalensis</li> <li>Mycale cecilia</li> <li>Mycale phylophylla</li> <li>Neopetrosia compacta</li> <li>Petrosia ficiformis (ASG)</li> <li>Pleraplysilla spinifera</li> <li>Pseudospongosorites suberitoides</li> <li>Sarcotragus fasciculatus</li> <li>Spongia officinalis</li> <li>Spongilla lacustris</li> <li>Tedania anhelans</li> <li>Tethya wilhelma</li> <li>Vaceletia crypta</li> <li>Xestospongia testudinaria</li> </ul> Hexactinellida: <ul> <li>Amphidiscella abyssalis</li> <li>Aulocalyx serialis</li> <li>Bolosoma cyanae</li> <li>Caulophacus discohexaster</li> <li>Farrea occa</li> <li>Farrea similaris</li> <li>Regadrella okinoseana</li> <li>Saccocalyx tetractinus</li> <li>Walteria leuckarti</li> </ul> Calcarea: <ul> <li>Clathrina coriacea</li> <li>Grantia compressa</li> <li>Leucetta chagosensis</li> <li>Leuconia nivea</li> <li>Sycon cyliatum</li> <li>Sycon coactum</li> </ul> Homoscleromorpha: <ul> <li>Corticium candelabrum</li> <li>Oscarella lobularis</li> <li>Oscarella pearsei</li> <li>Plakina jani</li> </ul>   The details about the read files used to assemble each transcriptome can be found at the CANTATA repository (<a href="https://gitlab.lrz.de/palmuc/cantata">https://gitlab.lrz.de/palmuc/cantata</a>)

Fig. 22 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 22. Dicyemodeca kukii sp. nov., photographs of syntype specimens on slide NSMT-Me-57: a–c, nematogen, anterior region; d, e, rhombogen, anterior region; f, vermiform embryos within axial cell; g, infusorigen; h, i, infusoriform embryos, horizontal section (h), sagittal section (i). Scale bars: 10 µm.

Fig. 25 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 25. Possible adhering processes of juvenile vermiform individuals of Dicyemennea leptocephalum; (a) juvenile individuals attached to the surface of the renal appendage by their calottes; (b) the calottes expand to be close to nearby calotte of individuals one another; (c) the calottes are adhering to one another.

Fig. 18 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 18. Dicyemennea desmocephalum sp. nov., photographs of syntype specimens on slide NSMT-Me-55: a, c, d, nematogen, entire, note that individuals adhere together with calottes (a), (c); b, g, rhombogen, entire, note that individuals adhere together with calottes (b); anterior region; e, vermiform embryos within axial cell; f, young nematgen, entire; f, h, infusorigen; i, j, infusoriform embryos, horizontal section (i), sagittal section (j). Scale bars: 20 µm in a–e, 10 µm in e, f, h–j.

Fig. 16 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 16. Dicyemennea moritakii sp. nov., photographs of syntype specimens on slide NSMT-Me-54: a, b, nematogen, anterior region; c, vermiform embryos within axial cell; d, e, rhombogen, anterior region; f, infusorigen; g, h, infusoriform embryos, horizontal section (g), sagittal section (h). Scale bars: 20 µm in a–e, 10 µm in f–h.

Fig. 15 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 15. Dicyemennea leptocephalum sp. nov., drawn from syntype specimens on slide NSMT-Me-53: a, nematogen, entire; b–d, rhombogen, entire; e, nematogen, anterior region; f, g, vermiform embryo within axial cell, cilia omitted (f), optical section (g); h, infusorigen; i–k, infusoriform embryos, dorsal view (i; cilia omitted), ventral view (j; cilia omitted), sagittal section (k). Scale bars: 100 µm in a–d, 50 µm in e, 10 µm in f–k.

Fig. 21 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 21. Dicyemennea tobaense sp. nov., drawn from syntype specimens on slide NSMT-Me-56: a, nematogen, entire; b, rhombogen, entire; c, d, nematogen, anterior region; e, rhombogen, anterior region; f, g, vermiform embryo within axial cell, cilia omitted (f), optical section (g); h, infusorigen; i–k, infusoriform embryos, dorsal view (i; cilia omitted), ventral view (j; cilia omitted), sagittal section (k). Scale bars: 100 µm in a, b, 10 µm in c–k.

Fig. 12 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 12. Dicyemennea megalosomum sp. nov., photographs of syntype specimens on slide NSMT-Me-52: a–c, nematogen, anterior region; d, e, rhombogen, anterior region; f, vermiform embryos within axial cell; g, infusorigen; h, i, infusoriform embryos, horizontal section (h), sagittal section (i). Scale bars: 50 µm in (d), 10 µm in a–c, e–i.

Fig. 10 in Eleven New Species of Dicyemids (Phylum Dicyemida) from Octopus longispadiceus and O. tenuicirrus (Mollusca: Cephalopoda: Octopoda) in Japanese Waters

Fig. 10. Dicyemennea acetabulum sp. nov., photographs of syntype specimens on slide NSMT-Me-51: a, nematogen, entire; b, nematogen, anterior region; c, vermiform embryos within axial cell; d–f, rhombogen, anterior region; g, infusorigen; h, i, infusoriform embryos, horizontal section (h), sagittal section (i). Scale bars: 50 µm in a, 5 µm in b–k.