Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
19
datasets available to search
ShareScore release 0.9.0
Dataset results
19 results for “Elisesione”
Fig. 2 in Elisesione problematica
Fig. 2. Durusdinium sp. dominance (%; symbols) and degree heating week (DHW in °C-weeks; shaded lines) of each group through time. (a) Transplanted group from Wanlitung (WLT) to the nuclear power plant outlet (OL) (WLT-OL transfer); (b) transplanted group from the nuclear power plant inlet (IL) to OL (IL-OL transfer); and (c) native group from the OL to OL (native OL), native group from the IL to IL (native IL), and native group from WLT to WLT (native WLT) for the 2014 reciprocal transplant experiment (2014RTE). (d) WLT- OL transfer and (e) native OL and native WLT for the 2015RTE. Each symbol in the data represents a single Platygyra verweyi colony. For 2015RTE data, colonies with similar dominance were merged into larger groups with sample numbers shown above the circle. Circles represent symbiont type D dominance of each colony at its last sampling time. (f) Survival rates at WLT-OL transfer and IL-OL transfer for different final Durusdinium sp. dominance values under each maximum DHW (based on 5 colonies in 2014RTE). Horizontal lines are 4 and 8 DHW.
Fig. 1 in Elisesione problematica
Fig. 1. Reciprocal transplant experiment (RTE) designs and temperature regimes at each study site. (a) Study sites in Kenting National Park. Blue arrows represent the 2014RTE and 2015RTE. (b) Weekly average temperatures recorded through time. (c) Daily seawater temperature fluctuations (°C) at each site. NA = no data. Different lowercase letters indicate significant differences in daily temperature ranges among sites (Kruskal-Wallis test, Dunn's post-hoc test, Bonferroni adjusted p values at α = 0.05). Bars within each box represent the median with boundaries representing the 25 to 75th percentiles. Whisker boundaries represent the 1.5x interquartile range and black dots represent outliers with values beyond that range. OL, nuclear power plant outlet; IL, nuclear power plant inlet; WLT, Wanlitung.
Fig. 4 in Elisesione problematica
Fig. 4. Tissue coverage growth and skeletal growth of each experiment group in the 2014 reciprocal transplantation experiment (2014RTE) and 2015RTE. (a) (top) Tissue coverage growth and (bottom) skeletal growth in the 2014RTE (n = 5 colonies in each group at each sampling time). (b) Tissue coverage growth in the 2015RTE. Arrows indicate the direction of transplantation. Data were measured at the end of each RTE relative to initial conditions (n = 30 colonies for each group at each sampling time unless stated otherwise). Different lowercase letters indicate a significant difference between groups (two-way ANOVA, Tukey's post-hoc test, Bonferroni adjusted p values at α = 0.05). For tissue coverage growth in the 2015RTE, there was an origin effect (F = 62.163, p <0.001) and location effect (F = 67.68, p <0.001), but no origin × location interaction (F = 0.695, p = 0.406). No statistics for the origin versus location effect were conducted in the 2014RTE because of a lack of sufficient sample size caused by mortality. †All samples were dead. OL-WLT transfer, group transplanted from the nuclear power plant outlet (OL) to Wanlitung (WLT); OL-IL transfer, group transplanted from the OL to the nuclear power plant inlet (IL).
Fig. 3 in Elisesione problematica
Fig. 3. Physiological parameters of experiment groups located at NPP-OL at each sampling time. (a) Total symbiont cell densities. (b) Chlorophyll a concentrations per cm2. (c) Total soluble protein concentrations. (d) Dark-adapted photochemical efficiency measured in 2014RTE. (n = 5 colonies for each group per sampling time unless stated otherwise). (e) Photochemical efficiency measured in 2015RTE. (n = 30 colonies for each group per sampling time unless stated otherwise). All data are presented as mean ± SD. Asterisks represent a significant difference of total symbiont density between each transplant group and the native group on each month. †All the samples were dead.
Fig. 8 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 8. Kainonereis polaris (Hartman, 1967) comb. n. Paratype atoke (USNM 55515). (A) anterior end, dorsal view; (B) close-up of prostomium; (C) anterior end, pharynx, ventral view; (D) tube; (E) notopodial homogomph spiniger, parapodium 13 (insert: closeup of teeth); (F) neuropodial sub-acicular heterogomph falciger, parapodium 13; (G) neuropodial sub-acicular heterogomph spiniger, parapodium 1; (H) parapodium 1, anterior view; (I) parapodium 3, anterior view; J parapodium 13, anterior view; K parapodium 37, anterior view. Scale bars: A-D = 0.5 mm; E = 20 µm; F, G = 10 µm; H-K = 0.2 mm.
Fig. 7 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 7. Kainonereis polaris (Hartman, 1967) comb. n. Holotype female (USNM 55514). (A) anterior end, dorsal view (arrows point lappets); (B) posterior end, dorsal view; (C) anterior end, pharynx, ventral view; (D) parapodium 7, anterior view; (E) parapodium 13, anterior view; (F) parapodium 19, anterior view; (G) parapodium 30, anterior view; (H) neuropodial supra-acicular heterogomph falciger, parapodium 13; (I) neuropodial sub-acicular heterogomph falciger, parapodium 13. Scale bars: A = 1 mm; B, C = 0.5 mm; D-G = 0.2 mm; H, I = 10 µm.
Fig. 4 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 4. Kainonereis chamberlini sp. n., A-C, F-H, J, K, holotype (USNM 1422199); D, E, I, paratype (UMML 22.1126). (A) whole specimen, dorsal view; (B) anterior end, dorsal view; (C) same, lateral view; (D) whole specimen, dorsal view; (E) same, lateral view; (F) neuropodial sub-acicular heterogomph spiniger, chaetiger 6; (G) neuropodial sub-acicular heterogomph falciger, parapodium 6; (H) parapodium 6, anterior view; (I) parapodium 11, anterior view; (J) parapodium 25, anterior view; (K) parapodium 40, anterior view. Scale bars: A, D = 1 mm; B, C, E = 0.5 mm; F, G = 10 µm; H-K = 0.1 mm.
Fig. 5 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 5. Kainonereis elytrocirra (Wu and Sun, 1979) comb. n. Paratype male (MBMCAS A-44). (A) anterior end, dorsal view; (B) whole specimen, dorsal view; (C) notopodial homogomph falciger, parapodium 4; (D) neuropodial supra-acicular heterogomph falciger, parapodium 4; (E) neuropodial sub-acicular heterogomph falciger, parapodium 7; (F) neuropodial supra-acicular heterogomph spiniger, parapodium 4; (G) parapodium 4, anterior view; (H) parapodium 6, anterior view; (I) parapodium 7, anterior view; (J) parapodium 19, anterior view; (K) parapodium 44, anterior view. Scale bars: A, B = 1 mm; C-F = 10 µm; G-K = 0.1 mm.
Fig. 2 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 2. Drawings from parapodia of Kainonereis species. K. alata A, B (USNM 19386); K. chamberlini sp. n. C (UMML 22.1126), D (USNM 1422199); K. elytrocirra comb. n. E, F (MBMCAS A-44); K. peltifera sp. n. G, H (LACM-AHF 7400p); K. polaris comb. n. I, J (USNM 55514). (A) parapodium 11, anterior view; (B) parapodium 40, anterior view; (C) parapodium 11, anterior view; (D) parapodium 25, anterior view; (E) parapodium 12, anterior view; (F) parapodium 20, anterior view; (G) parapodium10, anterior view; (H) parapodium 22, anterior view; (I) parapodium 13, posterior view; (J) parapodium 30, posterior view. Scale bars: A, B = 50 µm; C-H = 0.1 mm; I-J = 0.2 mm. E redrawn from Wu and Sun (1979:109). All chaetae omitted.
Fig. 3. Kainonereis alata Chamberlin, 1919 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 3. Kainonereis alata Chamberlin, 1919. Paratypes males (USNM 19386). (A) whole specimen, dorsal view; (B) anterior end, dorsal view; (C) anterior end, ventral view; (D) close-up of prostomium, dorsal view (arrow points beginning of ceratostyles); (E parapodium 3, anterior view; (F parapodium 5, anterior view; (G) parapodium 11, posterior view; (H) close-up of noto- and neuropodium, chaetiger 3 (dorsal and ventral cirri omitted); (I parapodium 40, posterior view; (J) notopodial homogomph falciger, parapodium 2; (K) pygidium, dorsal view. Abbreviations: An, antennae; Pa, palps. Scale bars: A = 1 mm; B, C = 0.5 mm; D, K = 0.1 mm; E-I = 50 µm; J = 10 µm.
Fig. 6 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 6. Kainonereis peltifera sp. n. A, B, holotype male (POLY-AHF 7400h); E, J-L, paratype male (POLY-AHF 7400p); C, D, F-I, M, N, paratype females (POLY-AHF 7400p). (A) anterior end, dorsal view; (B) close-up of chaetigers 5-7, dorsal view; (C) close-up of anterior end, dorsal view; (D) parapodium 1, anterior view; (E) parapodium 3, anterior view; (F) parapodium 6, anterior view; (G) parapodium 10, anterior view; (H) parapodium 22, anterior view; (I) parapodium 45, anterior view; (J) notopodial homogomph falciger, parapodium 3; (K) neuropodial sub-acicular falciger, parapodium 3; (L) neuropodial sub-acicular spiniger, parapodium 3; (M) neuropodial supra-acicular falciger, parapodium 10; (N) neuropodial sub-acicular falciger, parapodium 10. Scale bars: A, B, = 0.5 mm; C-I = 0.1 mm; J-N = 10 µm.
Fig. 1 in Elisesione imajimai Jimi & Eibye-Jacobsen & Salazar-Vallejo 2018, sp. nov.
Fig. 1. Morphology of Kainonereis Chamberlin, 1919 species. K. chamberlini sp. n. A-C, E (USNM 1422199); K. polaris comb. n. D (USNM 55514). (A) anterior end, dorsal view (transparency, 10x); (B) elytriform dorsal cirrus from mounted parapodium 6, anterior view; (C) same, non-mounted, lateral view; (D) parapodium 3, anterior view; (E) parapodium 40, anterior view. Abbreviations: Ac, anterior cirri; An, antennae; Cr, cirrostyle; DoLa, dorsal lamella of dorsal cirri; Di, disc; Jw, jaws; LDc, lower lamella of dorsal cirrus; LVc, lower lamella of ventral cirrus; NaL, neuroacicular ligule; NeV, neuropodial ventral ligule; NoD, notopodial dorsal ligule; NoV, notopodial ventral ligule; Ph, pharynx; PoL, neuropodial postchaetal lobe; Pr, prostomium; PreL, notopodial prechaetal lobe; St, stalk; UDc, upper lamella of dorsal cirrus; UVc, upper lamella of ventral cirrus; Vc, ventral cirrus; VeLa, ventral neuropodial lamella. Scale bars: A = 0.3 mm; B-E = 50 µm. All chaetae omitted.
Fig. 5 in Description of Elisesione imajimai sp. nov. From Japan (Annelida: Hesionidae) and A Redescription of E. problematica (Wesenberg-Lund, 1950) and Its Confirmation Within Hesionini
Fig. 5. Phylogenetic tree of Hesionidae based on COI, 16S, 18S and 28S sequences. Dysponetus caecus and Nereis pelagica were used as an 'outgroup'. Nodal support values (Maximum-likelihood (ML) bootstrap support [BS] value) are indicated on each branch.
Fig. 1 in Description of Elisesione imajimai sp. nov. From Japan (Annelida: Hesionidae) and A Redescription of E. problematica (Wesenberg-Lund, 1950) and Its Confirmation Within Hesionini
Fig. 1. Elisesione imajimai sp. nov., A-C, holotype (NSMT-Pol H-665); D, paratype (NSMT-Pol R: 604-2). (A) anterior end, dorsal view; (B) posterior end, dorsal view (arrow points to a lateral cushion); (C) prostomium, dorsal view (white arrows point to tips of antennae, black arrow points to left palp); (D) pharynx, ventral view. Scale bars: A-B = 5 mm; C = 3 mm; D = 2 mm.
Fig. 4 in Description of Elisesione imajimai sp. nov. From Japan (Annelida: Hesionidae) and A Redescription of E. problematica (Wesenberg-Lund, 1950) and Its Confirmation Within Hesionini
Fig. 4. Elisesione problematica (Wesenberg-Lund, 1950), holotype (ZMUC-POL-480). (A) chaetiger 5, right parapodium, posterior view (chaetae omitted); (B) same, dorsal cirrophore; (C) same, ventral cirrophore; (D) same, neurochaetae; (E) same, tip of ventral neurochaetal blade. Scale bars: A = 0.5 mm; B-D = 0.2 mm; E = 20 µm.
Fig. 2 in Description of Elisesione imajimai sp. nov. From Japan (Annelida: Hesionidae) and A Redescription of E. problematica (Wesenberg-Lund, 1950) and Its Confirmation Within Hesionini
Fig. 2. Parapodial features of Elisesione imajimai sp. nov., A-F, paratype (NSMT-Pol R:604-2), chaetiger 5, right parapodium, posterior view. (A) parapodium; (B) dorsal cirrophore; (C) ventral cirrus; (D) acicular lobe (arrow points to tip of acicular lobe); (E) neurochaetal bundle; (F) blade of ventral neurochaeta (inset: tip of blade). Scale bars: A = 1 mm; B-E = 300 μm; F = 100 μm; F (inset) = 5 μm.
Fig. 3 in Description of Elisesione imajimai sp. nov. From Japan (Annelida: Hesionidae) and A Redescription of E. problematica (Wesenberg-Lund, 1950) and Its Confirmation Within Hesionini
Fig. 3. Elisesione problematica (Wesenberg-Lund, 1950), holotype (ZMUC-POL-480). (A) anterior end, dorsal view; (B) posterior end, dorsal view; (C) head, dorsal view. Scale bars: A-C= 1 mm.
Figure 2 from: Salazar-Vallejo SI (2016) Elisesione, a new name for Wesenbergia Hartman, 1955, and the description of a new species (Annelida, Hesionidae). ZooKeys 632: 1-12. https://doi.org/10.3897/zookeys.632.9652
Figure 2 - Elisesione mezianei sp. n. Holotype (MNHN 1777). A Prostomium, dorsal view B Same, after methyl-green staining C Chaetiger 7, right parapodium, anterior view, dorsal cirrostyle removed, only base left on cirrophore (inset: close-up showing tips of double acicular lobe) D Chaetiger 7, neurochaetal blades, variably eroded; the one on the right has a wider handle due to optical interference, not really wider than the others. Scale bars A, B 0.27 mm, C 0.3 mm, D 20 µm.
Figure 1 from: Salazar-Vallejo SI (2016) Elisesione, a new name for Wesenbergia Hartman, 1955, and the description of a new species (Annelida, Hesionidae). ZooKeys 632: 1-12. https://doi.org/10.3897/zookeys.632.9652
Figure 1 - Elisesione mezianei sp. n. Holotype (MNHN 1777). A Anterior region, dorsal view B Anterior end, dorsal view C Posterior region, slightly oblique dorsal view D Pygidium. Scale bars A 1.6 mm, B 0.5 mm, C 1.2 mm, D 0.4 mm.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.
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.
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.
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.
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.