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Fig. 8 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 8. (A) Roboastra cf. tentaculata; (B) Gymnodoris alba; (C) Gymnodoris amakusana; (D) Gymnodoris citrina; (E) Gymnodoris impudica; (F) Gymnodoris inornata; (G) Gymnodoris nigricolor; (H) Gymnodoris sp.; (I) Polycera fujitai; (J) Polycera sp.; (K) Kaloplocamus acutus; (L) Kaloplocamus ramosus; (M) Plocamopherus ceylonicus; (N) Plocamopherus tilesii; (O) Pleurobranchaea brockii; (P) Berthellina citrina; (Q) Pleurobranchus forskalii; (R) Pleurobranchus peronii. Photographs by Tim Lam (A, C, F–H, L, M, O, P), AFCD (B, E, Q), Sze Yiu Ng (D, K), WK Chow (I), Gomen See (J, N) and Wai Hong Yiu (R).

opencc-by-4.0Nov 2022View details →
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Fig. 5 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 5. (A) Ceratosoma trilobatum; (B) Hypselodoris apolegma; (C) Hypselodoris confetti; (D) Hypselodoris decorata; (E) Hypselodoris festiva; (F) Hypselodoris katherinae; (G) Hypselodoris maritima; (H) Hypselodoris placida; (I) Mexichromis multituberculata; (J) Mexichromis similaris; (K) Thorunna florens; (L) Atagema intecta; (M) Atagema spongiosa; (N) Atagema sp.; (O) Carminodoris pustulata; (P) Jorunna parva; (Q) Jorunna cf. ramicola; (R) Platydoris ellioti. Photographs by Tim Lam (A, C, D, F, H–J, L–Q), AFCD | Wai Hong Yiu (B), Sze Yiu Ng (E, G), Alice Au (K) and Caron Ka Lok Wong (R).

opencc-by-4.0Nov 2022View details →
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Fig. 4 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 4. (A) Chromodoris mandapamensis; (B) Chromodoris orientalis; (C) Chromodoris striatella; (D) Diversidoris aurantionodulosa; (E) Doriprismatica atromarginata; (F) Glossodoris acosti; (G) Goniobranchus aureopurpureus; (H) Goniobranchus collingwoodi; (I) Goniobranchus fidelis; (J) Goniobranchus geometricus; (K) Goniobranchus hintuanensis; (L) Goniobranchus setoensis; (M, N) Goniobranchus sinensis; (O) Goniobranchus tumuliferus; (P) Goniobranchus cf. verrieri; (Q) Verconia hongkongiensis; (R) Verconia nivalis. Photographs by Anniqua Law (A), Sze Yiu Ng (B, O), Simon Lorenz (C), Tim Lam (D–G, I, L, M, P–R), AFCD | Ho Nam Lam (H), AFCD (J), Cherie Wong (K) and AFCD | Yat Sing Lau (N).

opencc-by-4.0Nov 2022View details →
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Fig. 6 in Fig. 2 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 6. Changes in PP1 enzymatic activity in Bombyx eggs. A, diapause eggs; B, non-diapause eggs; C, eggs whose diapause initiation was prevented by HCl; D, eggs in which diapause had been terminated by chilling. Egg extracts from each stage were prepared, and PP1 enzymatic activity was determined with a PP1 assay kit. The data represent mean ± SEM of four separate assays.

opencc-by-4.0Nov 2022View details →
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Fig. 11 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 11. (A) Elysia sp. 1; (B) Elysia sp. 2; (C) Thuridilla gracilis. Photographs by Tim Lam (A, B) and AFCD (C).

opencc-by-4.0Nov 2022View details →
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Fig. 7 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 7. (A) Trapania aurata; (B) Trapania darvelli; (C) Trapania japonica; (D) Trapania miltabrancha; (E) Dendrodoris arborescens; (F, G) Dendrodoris fumata; (H) Dendrodoris krusensternii; (I, J) Dendrodoris nigra; (K) Dendrodoris sp.; (L) Doriopsilla miniata; (M) Phyllidia ocellata; (N) Phyllidia varicosa; (O) Phyllidiella pustulosa; (P) Phyllidiopsis cardinalis; (Q) Kalinga ornata; (R) Tambja cf. pulcherrima; Photographs by Tim Lam (A–C, G, K, N, Q, R), Dik Cheung (D), Sze Yiu Ng (E), AFCD (F, J, M, P) and Gomen See (H, I, L, O).

opencc-by-4.0Nov 2022View details →
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Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 3. (A) Phestilla fuscostriata; (B) Phestilla goniophaga; (C) Phestilla lugubris; (D, E) Phestilla melanobrachia; (F) Phestilla sp.; (G) Trinchesia ornata; (H) Trinchesia yamasui; (I) Trinchesia sp.; (J) Unidentia aliciae; (K) Madrella ferruginosa; (L) Marionia echinomuriceae; (M) Marionia cf. rubra; (N) Tritonia sp.; (O) Actinocyclus papillatus; (P) Chromodoris dianae; (Q) Chromodoris lineolata; (R) Chromodoris magnifica. Photographs by AFCD | Henry Tat Heng Ho (A), Gary To (B), Tim Lam (C, F, J, K, N), AFCD (D, E, H, L, M, O, P), Grape Tang (G), Alice Au (I), Gomen See (Q) and AFCD | Chi Hung Yip (R).

opencc-by-4.0Nov 2022View details →
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Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 6. (A) Rostanga bifurcata; (B) Rostanga dentacus; (C) Sclerodoris apiculata; (D) Doriopsis granulosa; (E) Doris sp.; (F) Homoiodoris japonica; (G) Aegires exeches; (H) Aegires villosus; (I) Diaphorodoris mitsuii; (J) Goniodoridella savignyi; (K) Goniodoris felis; (L) Goniodoris sp.; (M) Okenia barnardi; (N) Okenia hiroi; (O) Okenia japonica; (P) Okenia pilosa; (Q) Okenia plana; (R) Okenia sp. Photographs by Tim Lam (A–G, I– M, O–R), Grape Tang (H) and Gary To (N).

opencc-by-4.0Nov 2022View details →
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Fig. 2 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 2. (A) Dermatobranchus albus; (B) Dermatobranchus tongshanensis; (C) Dermatobranchus sp. 1; (D) Dermatobranchus sp. 2; (E) Bornella stellifera; (F) Doto sp. 2; (G, H) Doto sp. 3; (I) Lomanotus vermiformis; (J) Lomanotus sp.; (K) Notobryon wardi; (L) Melibe cf. japonica; (M) Abronica purpureoanulata; (N) Coryphellina lotos; (O) Flabellina sp.; (P) Eubranchus rubropunctatus; (Q) Samla bicolor; (R) Catriona pinnifera. Photographs by Tim Lam (A–E, G, I, L, M, R), AFCD (F, H, P), Alice Au (J), Tom Chan (K), Gary To (N), AFCD | Henry Tat Heng Ho (O), Henry Li (P) and Markus Rummel (Q).

opencc-by-4.0Nov 2022View details →
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Fig. 9 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 9. (A) Aplysia argus; (B) Aplysia concava; (C) Aplysia japonica; (D) Aplysia kurodai; (E) Aplysia nigrocincta; (F) Aplysia oculifera; (G) Aplysia sp.; (H) Bursatella leachii; (I) Dolabrifera dolabrifera; (J) Haloa japonica; (K) Chelidonura amoena; (L) Chelidonura hirundinina; (M) Niparaya regiscorona; (N) Niparaya sp.; (O) Philinopsis falciphallus; (P) Philinopsis speciosa; (Q) Tubulophilinopsis lineolata; (R) Tubulophilinopsis pilsbry. Photographs by Tim Lam (A–D, G, K, M, O, P), Sze Yiu Ng (E), Gomen See (F, H, I), AFCD (J), Bell Kwok (L), Alice Au (N), Grape Tang (Q) and Peggie Hon (R).

opencc-by-4.0Nov 2022View details →
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Fig. 4 in Fig. 2 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 4. Western blot analysis of protein levels of PP1-C, PNUTS, and PP4-C in non-diapause eggs. Egg lysates from each stage after oviposition were prepared and subjected to an immunoblot analysis with anti-PP1α (PP1), anti-PNUTS (PNUTS), anti-PP4-C (PP4), and anti-HSP 90 (HSP) antibodies. Lysates from a quarter of one egg were used for each lane. Molecular weight markers are shown on the right side of the gel (A). Results shown in the upper panel are representative of four independent experiments. Quantified protein levels relative to HSP were standardized to levels from the first day after oviposition. Different letters above the bars indicate significant differences (ANOVA followed by Tukey's test).

opencc-by-4.0Nov 2022View details →
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Fig. 2 in Fig. 2 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 2. Effect of HCl treatment on protein levels of PP1-C, PNUTS, and PP4-C during the first 8 days after treatment. Diapause-destined eggs that had been incubated at 25°C for 20 h after oviposition were treated with HCl and then incubated at 25°C. Egg lysates from each stage were prepared and subjected to an immunoblot analysis with anti-PP1α (PP1), anti-PNUTS (PNUTS), anti-PP4-C (PP4), and HSP 90 (HSP) antibodies. Lysates from a quarter of one egg were used for each lane. Molecular weight markers are shown on the right side of the gel (A). Results shown in the upper panel are representative of four independent experiments. Quantified protein levels relative to HSP were standardized to levels from the first day after HCl treatment. Different letters above the bars indicate significant differences (ANOVA followed by Tukey's test).

opencc-by-4.0Nov 2022View details →
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Fig. 1 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 1. (A) Hydatina physis; (B) Anteaeolidiella lurana; (C) Baeolidia salaamica; (D) Bulbaeolidia alba; (E) Cerberilla ambonensis; (F) Spurilla braziliana; (G) Caloria indica; (H) Cratena cf. poshitraensis; (I) Cratena sp.; (J) Facelina sp.; (K) Favorinus sp.; (L) Phidiana anulifera; (M) Phidiana militaris; (N) Sakuraeolis enosimensis; (O) Sakuraeolis sp.; (P) Godiva cf. rachelae; (Q) Phyllodesmium magnum; (R) Phyllodesmium opalescens. Photographs by Harmon Wong (A), Tim Lam (B–D, G–I, K, L, P, R), Rachel Wong (E), AFCD (F, Q), Henry Li (J), Caron Ka Lok Wong (M), Gary To (N) and Alice Au (O).

opencc-by-4.0Nov 2022View details →
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Fig. 2. Pseudohelice annamalai n in Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 2. Pseudohelice annamalai n. sp. A, carapace; B, outer view of male left cheliped; C, left male infraorbital ridge; D, E, left female infraorbital ridge (D, form I; E, form II); F, G, dorsal view of right G1; H, I, ventral view of right G1; J, K, right vulva (J, form I; K, form II). A, B, male, CASAU CR-1013 (18.9 × 15.2 mm); C, F–I, holotype male, CASAU CR 1011 (17.3 × 14.6 mm); D, female, NCHUZOOL 17049 (18.8 × 16.4 mm); E, J, female, ZRC 2022.0189 (18.1 × 15.4 mm); K, female, NCHUZOOL 17049 (13.9 × 11.6 mm).

opencc-by-4.0Sep 2022View details →
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Fig. 1. Pseudohelice annamalai n in Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 1. Pseudohelice annamalai n. sp. with preserved coloration. A, dorsal view of male; B, ventral view of male; C, dorsal view of female; D, ventral view of female. A, B, holotype, CASAU CR-1011 (17.3 × 14.6 mm); C, D, NCHUZOOL 17049 (14.3 × 12.5 mm).

opencc-by-4.0Sep 2022View details →
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Fig. 5. A in Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 5. A Bayesian inference (BI) tree for species of Pseudohelice and the outgroups, based on the cytochrome c oxidase subunit I (COI) gene. Probability values at the nodes represent support values for BI, maximum likelihood (ML) and maximum parsimony (MP). For haplotype names, see table 1.

opencc-by-4.0Sep 2022View details →
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Fig. 4 in Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 4. Color in life of Pseudohelice annamalai n. sp. (A–G) from higher intertidal zone of the Vellar River estuary, Tamil Nadu, India. A, B, dorsal view of male; C, D, frontal and dorsal views of female, respectively; E, F, dorsal and frontal views of an ovigerous female, respectively; G, male at the burrow entrance near mangrove pneumatophores; H, burrow in the habitat. A, CASAU CR-1012 (18.2 × 15.5 mm); B, CASAU CR-1016 (18.7 × 15.4 mm), C–F, specimens not collected; G, NCHUZOOL 17049 (18.2 × 16.8 mm).

opencc-by-4.0Sep 2022View details →
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Fig. 3 in Fig. 6 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 3. Habitats of Pseudohelice annamalai n. sp. A, higher intertidal zone of the Vellar River estuary, in front of the Centre of Advanced Study in Marine Biology, Tamil Nadu, southeastern India; B, artificial mangroves of Rhizophora sp. and Avicennia sp., in the margin of Vellar River.

opencc-by-4.0Sep 2022View details →
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Fig. 5. A in Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 5. A major ocean current flow pattern in Korean waters (A) and a possible scenario for the introduction and expansion of C. brevipedalia in the Korean coasts (B). The big cycles represent the haplotype compositions sampled in the present study, while the small cycles indicate the current distribution of C. brevipedalia in Korean waters. The big orange cycle represents clade A haplotypes while the blue cycle represents clade B haplotypes. Moreover, the orange color in clade B represents the shared haplotypes between southern coastal regions (SCR) and eastern coastal regions (ECR). JCR; Japanese coastal regions.

opencc-by-4.0Oct 2022View details →
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Fig. 2 in Fig. 3 in Garypus sanasai Lin, Huang & Chang 2022, sp. nov.

Fig. 2. Maximum likelihood and Bayesian inference phylogenetic tree, showing taxonomic relationship of C. brevipedalia and other jelly fish species. Numbers separated by a slash above each branch are posterior probabilities (on the left side) followed by bootstrap values (on the right side). Nodal support of less than 50% is not shown.

opencc-by-4.0Oct 2022View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record