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opencc-by-4.0Jun 2015View details →

Figure 6 in Spatiotemporal distribution of planktonic copepod communities in Tokyo Bay where Oithona davisae Ferrari and Orsi dominated in mid-1980s

Figure 6. Horizontal distributions of the identified community groups in Tokyo Bay (the letters in parentheses in legends show the indicator species).

Fig. 4 in Redescription of the Sea Anemone Exocoelactis actinostoloides (Cnidaria: Anthozoa: Actiniaria) Based on a Topotypic Specimen Collected from Tokyo Bay, Japan

Fig. 4. Mesenterial arrangement of Exocoelactis actinostoloides (CMNH ZG 05926). A, diagrammatic image; B, gross transverse section of column at level of pharynx; C, histological transverse section of approximately one-third of whole cycle in lower part of column, just under pharynx. Abbreviations: I–V, pairs of mesenteries of first to fifth cycle respectively; d, pairs of directive mesenteries; g, gonad; p, pharynx; s, siphonoglyph. Scale bars: 10 mm.

Fig. 1 in Redescription of the Sea Anemone Exocoelactis actinostoloides (Cnidaria: Anthozoa: Actiniaria) Based on a Topotypic Specimen Collected from Tokyo Bay, Japan

Fig. 1. Localities of Exocoelactis actinostoloides (Wassilieff, 1908) around Sagami Bay, Japan. Jogashima and Enoshima are the type localities of Ex. actinostoloides and Cymbactis maxima Wassilieff, 1908, respectively.

Fig. 3 in Redescription of the Sea Anemone Exocoelactis actinostoloides (Cnidaria: Anthozoa: Actiniaria) Based on a Topotypic Specimen Collected from Tokyo Bay, Japan

Fig. 3. Exocoelactis actinostoloides (CMNH-ZG 05926) from Uraga Strait, mouth of Tokyo Bay, live. A, oral view; B, lateral view; C, oral view around mouth; D, lateral view of upper part of column. s, siphonoglyph. Scale bars (lower right in each image): 20 mm.

Fig. 7 in Redescription of the Sea Anemone Exocoelactis actinostoloides (Cnidaria: Anthozoa: Actiniaria) Based on a Topotypic Specimen Collected from Tokyo Bay, Japan

Fig. 7. Cnidae from tentacle, column, pharynx, and mesenterial filaments of Exocoelactis actinostoloides (CMNH-ZG 05926). For letters a–m, refer to Table 1. Scale bar: 50 µm.

Fig. 9 in Redescription of the Sea Anemone Exocoelactis actinostoloides (Cnidaria: Anthozoa: Actiniaria) Based on a Topotypic Specimen Collected from Tokyo Bay, Japan

Fig. 9. Maximum likelihood tree of total 1094 base pairs of concatenated 12S rDNA and 16S rDNA, showing placement of newly obtained sequences from Exocoelactis actinostoloides (CMNH-ZG 05926) among previously published GenBank sequences. Values of ML bootstrap values>60% are shown at the respective nodes; monophylies with Bayesian posterior probabilities of>0.90 in Bayseian tree are shown by thick branches. Ex. actinostoloides is shown in a bold and larger font. Species names corresponding to sequences from previous studies are shown in regular font. Black and white stars indicate members of the family Actinostolidae sensu Rodríguez et al. (2008) and Exocoelactinidae, respectively.

Fig. 8 in Redescription of the Sea Anemone Exocoelactis actinostoloides (Cnidaria: Anthozoa: Actiniaria) Based on a Topotypic Specimen Collected from Tokyo Bay, Japan

Fig. 8. Size distribution of cnidae of Exocoelactis actinostoloides (CMNH-ZG 05926). Squares indicate ranges of length and width reported by Arellano and Fautin (2001: 654, table 2): orange squares, holotype; green squares, other specimens investigated by Arellano and Fautin (2001). "n" is number of capsules measured. For letters a–m, refer to Table 1 and Fig. 7.

Fig. 6 in Redescription of the Sea Anemone Exocoelactis actinostoloides (Cnidaria: Anthozoa: Actiniaria) Based on a Topotypic Specimen Collected from Tokyo Bay, Japan

Fig. 6. Scanning electric microscope images of musculature of Exocoelactis actinostoloides (CMNH-ZG 05926). A, sphincter; B, enlarged detail of A (area within rectangle); C, tentacular longitudinal muscle; D, enlarged detail of C (area within rectangle). Abbreviations: ed, epidermis; gd, gastrodermis; mg, mesogloea; mf, muscle fibers; sm, sphincter muscle; tm, tentacular longitudinal muscle. Scale bars: 200 µm for A, C; 10 µm for B, D.

opencc-by-4.0May 2015View details →

Fig. 3. Pennatulicola piscatorius n in A New Species of Pennatulicola Humes and Stock (Copepoda: Cyclopoida: Rhynchomolgidae) Associated with a Pennatulacean from Tokyo Bay, Japan

Fig. 3. Pennatulicola piscatorius n. sp. Female, paratype: A, leg 4 (arrowhead indicates inner terminal process that is usually absent); B, exopod of leg 5; C, genital aperture. Male, paratype: D, habitus, dorsal; E, urosome, ventral; F, right caudal ramus, ventral; G, maxilliped; H, exopod of leg 5. Scale bars: A–C, E, H, 0.05 mm; D, 0.1 mm; F, G, 0.02 mm.

opencc-by-4.0May 2015View details →

Fig. 2. Pennatulicola piscatorius n in A New Species of Pennatulicola Humes and Stock (Copepoda: Cyclopoida: Rhynchomolgidae) Associated with a Pennatulacean from Tokyo Bay, Japan

Fig. 2. Pennatulicola piscatorius n. sp., female, paratype. A, mandible; B, paragnath; C, maxillule; D, maxilla (Roman numerals I–III indicate setae I–III); E, maxilliped; F, leg 1; G, leg 2; H, leg 3. Scale bars: A–E, 0.02 mm; F–H, 0.05 mm.

Fig. 2 in A New Species of the Sand-burrowing Dogielinotidae, Haustorioides furotai, from Tokyo Bay, Japan (Crustacea: Amphipoda)

Fig. 2. Haustorioides furotai Ogawa, sp. nov., photographs of live animals. A, Paratype female (NSMT-Cr 28351), 7.2 mm; B, holotype, male (NSMT-Cr 28350), 7.2 mm. Scale bar: 1 mm.

Fig. 1. Map showing a in A New Species of the Sand-burrowing Dogielinotidae, Haustorioides furotai, from Tokyo Bay, Japan (Crustacea: Amphipoda)

Fig. 1. Map showing a collecting site, Banzu tidal flat, Kisarazu City, Chiba Prefecture, Japan (filled circle).

Fig. 8 in A New Species of the Sand-burrowing Dogielinotidae, Haustorioides furotai, from Tokyo Bay, Japan (Crustacea: Amphipoda)

Fig. 8. Haustorioides furotai Ogawa, sp. nov., paratype, female (NSMT-Cr 28351), 9.0 mm. A, Left pereopod 4; B, left pereopod 5.

Fig. 4 in A New Species of the Sand-burrowing Dogielinotidae, Haustorioides furotai, from Tokyo Bay, Japan (Crustacea: Amphipoda)

Fig. 4. Haustorioides furotai Ogawa, sp. nov., holotype, male (NSMT-Cr 28350), 7.2 mm A, Left gnathopod 1; B, palm of left gnathopod 1; C, left gnathopod 2; D, left pereopod 3; E, left pereopod 4.

Fig. 5 in A New Species of the Sand-burrowing Dogielinotidae, Haustorioides furotai, from Tokyo Bay, Japan (Crustacea: Amphipoda)

Fig. 5. Haustorioides furotai Ogawa, sp. nov., holotype, male (NSMT-Cr 28350), 7.2 mm. A, Left pereopod 5; B, left pereopod 6; C, left pereopod 7.

Fig. 7 in A New Species of the Sand-burrowing Dogielinotidae, Haustorioides furotai, from Tokyo Bay, Japan (Crustacea: Amphipoda)

Fig. 7. Haustorioides furotai Ogawa, sp. nov., paratype, female (NSMT-Cr 28351), 9.0 mm. A, Left gnathopod 2; B, left pereopod 3.

opencc-by-4.0Dec 2017View details →

Fig. 1 in Prevalence of avian haemosporidia among injured wild birds in Tokyo and environs, Japan

Fig. 1. Locations of the four facilities in the Kanto region that samples were collected. A. Kanagawa Prefecture Natural Conservation Center, B. Inokashira Animal Hospital, C. Gyotoku Wild Bird Hospital, D. Bird Clinic Kanesaka Animal Hospital.

opencc-by-4.0Dec 2017View details →

Fig. 2 in Prevalence of avian haemosporidia among injured wild birds in Tokyo and environs, Japan

Fig. 2. Hemacolor ® stained blood smears from rescued birds: (a) Plasmodium sp. from Cyanopica cyanus, (b) P. reluctum from Hypisipetes amaurotis, (c) P. circumflexum from Fulica atra, (d) Haemoproteus sp. from Hypisipetes amaurotis, (e) Haemoproteus sp. from Larus canus, (f) H. minutus from Turdus cardis, (g) Leucocytozoon sp. from Anas acuta, (h) Leucocytozoon sp. from Aythya marila.

opencc-by-4.0Jun 2021View details →

Data for: A further source of Tokyo earthquakes and Pacific Ocean tsunamis

This data repository contains the location of cores collected as part of this study, the microfossil and radiocarbon results from those cores, and fault parameters used in eleven historical and hypothetical tsunami simulations for Kujukuri, Japan (Boso Peninsula). The work is supported by the Geological Survey of Japan, National Institute of Advanced Industrial Science and Technology (AIST) and in part by grants awarded to J.E.P. [National Science Foundation (EAR-1303881 and 1624612), Natural Sciences and Engineering Council of Canada (NSERC), Canada Research Chair (CRC) program, and  Japan Society for the Promotion of Science (JSPS) International Research Fellow program at the Geological Survey of Japan (PE14038)]; A.C.P. [Science Foundation Ireland Career Development Award (17/CDA/4695),  Investigator Award (16/IA/4520), Marine Research Programme funded by the Irish Government, co-financed by the European Regional Development Fund (Grant-Aid Agreement No. PBA/CC/18/01), European Union’s Horizon 2020 research and innovation programme under grant agreement No 818144, and SFI Research Centre (16/RC/3872 and 12/RC/2289_P2); and B.P.H. [Singapore Ministry of Education Academic Research Fund (MOE2019-T3-1-004), National Research Foundation Singapore, and Singapore Ministry of Education, under the Reseach Centers of Excellence initiative].