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1,947 results for “Proposals”
FIGURES 42–45 in Monogenoids (Polyonchoinea, Dactylogyridae) from Hydrolycus armatus (Characiformes, Cynodontidae) with the description of a new species of Rhinoxenus and the proposal of a new genus from the Xingu River, Pará, Brazil
FIGURES 42–45. The copulatory complex of species of Mymarothecioides n. gen. 42. Mymarothecioides ararai n. sp. 43. Mymarothecioides xinguensis n. sp. 44. Mymarothecioides altamirensis n. sp. 45. Mymarothecioides germanoi n. sp.
FIGURES 10–17. Mymarothecioides xinguensis n in Monogenoids (Polyonchoinea, Dactylogyridae) from Hydrolycus armatus (Characiformes, Cynodontidae) with the description of a new species of Rhinoxenus and the proposal of a new genus from the Xingu River, Pará, Brazil
FIGURES 10–17. Mymarothecioides xinguensis n. sp. 10. Holotype whole-mount (ventral) (composite). 11. Copulatory complex. 12. Hook pair 1–4, 6–7. 13. Hook pair 5. 14. Ventral bar. 15. Dorsal bar. 16. Ventral anchor. 17. Dorsal anchor.
FIGURES 1–9. Rhinoxenus cachorra n in Monogenoids (Polyonchoinea, Dactylogyridae) from Hydrolycus armatus (Characiformes, Cynodontidae) with the description of a new species of Rhinoxenus and the proposal of a new genus from the Xingu River, Pará, Brazil
FIGURES 1–9. Rhinoxenus cachorra n. sp. 1. Holotype whole-mount (ventral) (composite). 2. Copulatory complex. 3. Hook pair 2. 4. Hook pair 1. 5. Hook pair 3–7. 6. Ventral bar (view, ventral). 7. Ventral bar (view, dorsal). 8. Ventral anchor. 9. Dorsal anchor.
FIGURES 18–26. Mymarothecioides altamirensis n in Monogenoids (Polyonchoinea, Dactylogyridae) from Hydrolycus armatus (Characiformes, Cynodontidae) with the description of a new species of Rhinoxenus and the proposal of a new genus from the Xingu River, Pará, Brazil
FIGURES 18–26. Mymarothecioides altamirensis n. sp. 18. Composite whole-mount (ventral). 19. Copulatory complex. 20. Hook pair 1–4. 21. Hook pair 5. 22. Hook pair 6–7. 23. Ventral bar. 24. Dorsal bar. 25. Ventral anchor. 26. Dorsal anchor.
Fig. 2 Conceptual differences among proposed niche overlap analyses. Imagine a in A novel method to calculate climatic niche similarity among species with restricted ranges-the case of terrestrial Lycian salamanders
Fig. 2 Conceptual differences among proposed niche overlap analyses. Imagine a set of three species with different preferences along an environmental gradient. Using SDM projections, it is possible to derive for each species a probability distribution across the gradient. Comparing two species as proposed by Warren et al. (2008), the overlap (grey area in the middle panel) of their respective probability distributions in geographic space is computed (pair-wise niche overlap). In our jackknife approach, a probability distribution derived from all species records is compared to a probability distribution derived from all minus one species. The 1−the resulting overlap value reflects the relative contribution of the omitted species to the entire probability distribution (grey area in the lower panel) and can be used as measure to rank all species when omitting them iteratively. Note that these specific indices are comparable only across each method but not among the different approaches
Figure 2. Proposed general secondary structure model for the ITS1–5.8S rDNA–ITS2 in A revised taxonomy and phylogeny of opalinids (Stramenopiles: Opalinata) inferred from the analysis of complete nuclear ribosomal DNA genes
Figure 2. Proposed general secondary structure model for the ITS1–5.8S rDNA–ITS2–LSU rDNA of Opalinida* The expansion segments (ES#L) containing helices (in red) where there are important differences between genera are annotated. Colour code: yellow* ITS1 region; blue* 5.8S rRNA; magenta* ITS2 region; grey* LSU rRNA.
Key SOILL actions to consider for proposals when setting up Soil Health Living Labs (SHLLs) & Lighthouses (LHs)
<p>The infographic "Key SOILL Actions to Consider for Proposals When Setting Up Soil Health Living Labs (SHLLs) & Lighthouses (LHs)" provides a strategic overview for potential applicants to the Horizon Europe topics funding the establishement of the Soil Health Living Labs on the essential activities and commitments required for effective participation in the SOILL, the EU-funded Support Structure for the Soil Health Living Labs and Lighthouses. Designed in response to a need highlighted by the key stakeholders, this visual guide ensures that applicants consider the necessary time and budget for involvement in SOILL events, training, and collaborative efforts. The infographic categorises actions into in-person, in-person/online, and online-only engagements, offering a clear understanding for integrating these elements into the proposals. This tool has been realised with aim to fulfil the SOILL and NATI00NS project's missions, aiding in the preparation and alignment of SHLL/LH proposals with SOILL's overarching goals.</p>
FIGURE 8 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURE 8. Gibsmithia eilatensis sp. nov. A–B) Mature corncob-like spermatangial heads. A) Slide DG220-1. Scale bar 50 μm. B) Slide DG220-1, scale bar 20 μm. C) Young and mature tetrasporangia. Slide DG219-1. Scale bar 20 μm. D–E) Terminal and lateral tetrasporangial initials growing on lateral assimilatory filaments, and decussate and cruciate tetrasporangia. D) Slide DG219-1. Scale bar 50 μm. E) Slide DG219-1. Scale bar 20 μm.
FIGURES 5 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURES 5. Range of habits of Gibsmithia hawaiiensis from the Hawaiian Islands (dry herbarium specimens). Main Hawaiian Islands: A) DG261, Hawaii; B) DG255, Hawaii; C) DG253, Oahu; D) DG267, Oahu. Northwestern Hawaiian Islands: E) DG258; F) DG218. Scale bar = 1.0 cm.
FIGURE 3 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURE 3. Consensus phylogram obtained from the Bayesian Inference analysis of the concatenated dataset (rbcL, UPA and COI- 5P). Numbers besides nodes indicate posterior-probabilities (BI) and bootstrap values (ML), respectively. Scale bar indicates number of substitutions per site. A to E represent the different lineages observed. Numbers represents the respective marine provinces: 1) Hawaii; 2) Southeast Polynesia; 3) Sunda Shelf; 4) Western Coral Triangle; 5) Tropical Northwestern Pacific; 6) Western Indian Ocean; 7) Red Sea and Gulf of Aden.
FIGURE 2 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURE 2. Reported distribution of Gibsmithia hawaiiensis prior to this study (grey shade), based on records listed in AlgaeBase (Guiry & Guiry 2016): Africa: South Africa, Tanzania; Indian Ocean Islands: Seychelles; Asia: China, Japan, Taiwan; South-east Asia: Indonesia, Philippines, Vietnam; Australia and New Zealand: Australia, Coral Sea Islands Territory, Papua New Guinea, Queensland, Western Australia; Pacific Islands: Central Polynesia, Federated States of Micronesia, Fiji, French Polynesia, Guam, Hawaiian Islands, Mariana Islands, Northern Hawaiian Islands, Republic of Palau. Collection sites are marked with shapes corresponding to the different lineages from Fig. 3.
FIGURE 1 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURE 1. In situ habits of Gibsmithia hawaiiensis complex. A) DG234, Eilat, Israel. B) SGAD0509563, Kepulauan Seribu, Indonesia. C) SGAD0911460, Ternate, Indonesia. D) TIG001, Pulau Tiga, Malaysia. E) SGAD1205119, Johor, Malaysia. F) SGAD0712185, Raja Ampat, Indonesia. G) SGAD1206005, Labuan, Malaysia. Four individuals, each comprising one stipe and one to a few lobes. H) LEM03, Bitung, Indonesia. Scale bar 1 cm. Photo credits: A) T. Sauvage; B) A. Gittenberger; C, E–G) S.G.A. Draisma; D) M.A.S. Hussein; H) B.T. Reijnen.
FIGURE 7 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURE 7. Gibsmithia eilatensis sp. nov. Early post-fertilization stages. A) Vegetative lateral branch (arrowhead) on basal cell of carpogonial filament, and curved hypogynous cell (arrow). Slide DG210-4. Scale bar 50 μm. B) Presumed early fertilization stage showing lateral extension of carpogonium and hypogynous cell (arrowhead). Slide DG210-1. Scale bar 50 μm. C) Auxiliary cell branch. Slide DG234-4. Scale bar 50 μm. D) Unsegmented incoming connecting filament (ic) partly and laterally fused to auxiliary cell, and unseptated outgoing connecting filament (oc). Slide DG234-2. Scale bar 100 μm. E) Incoming connecting filament (ic) segment partly fused with auxiliary cell, and outgoing connecting filament (oc) segment (arrow) partly fused with nearby auxiliary cell. Slide DG234- 3. Scale bar 50 μm. F) Gonimoblast initial (arrow) developed from the short segment partly fused to auxiliary cell, between incoming connecting filament (ic) and outgoing connecting filament (oc). Slide DG234-3. Scale bar 50 μm. G–H) Multiple gonimoblast initials cut off bilaterally from connecting filament segment (arrow) fused to auxiliary cell. G) Slide DG234-3. Scale bar 50 μm. H) Slide DG234-5. Scale bar 50 μm. I) Young clusters of spermatangia (arrow) formed terminally and laterally in assimilatory filaments. Slide DG220-1. Scale bar 50 μm.
FIGURE 4 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURE 4. In vivo habits of G. eilatensis sp. nov. Specimens growing: A) attached to coral reef surface (DG219; isotype), B) between coral heads (DG210) and C) under a coral wall (DG234; holotype). Scale bar = 1.0 cm
FIGURE 6 in Multilocus phylogeny reveals Gibsmithia hawaiiensis (Dumontiaceae, Rhodophyta) to be a species complex from the Indo-Pacific, with the proposal of G. eilatensis sp. nov.
FIGURE 6. Gibsmithia eilatensis sp. nov. A) Holotype, female gametophyte, DG234, Eilat, Israel. B) Assimilatory filaments comprised of main percurrent filaments (arrow), cortical filaments (arrowhead) and rhizoidal filaments (double arrowhead). Rhizoidal filaments with cells connected to neighboring rhizoidal cells. Slide DG219-2. Scale bar 200 μm. C) Female pre-fertilization stages among elongated, narrow assimilatory filaments. Slide DG234-3. Scale bar 200 μm. D) Hairlike extensions from apical cortical cells. Slide DG210-2. Scale bar 50 μm. E) Branched and unbranched "seirospore" filaments. Slide DG210-5. Scale bar 50 μm. F) Carpogonial branch laterally positioned on assimilatory filaments, with straight and obliquely (arrow) directed trichogynes. Slide DG210-1. Scale bar 50 μm. G) Carpogonial branch with laterally extended hypogynous cell (double arrowhead), small subhypogynous cell (arrowhead) and conical carpogonium (arrow) with straight trichogyne. Slide DG210-4. Scale bar 50 μm.
Figures 4-9. Calliphara bipunctata LEHMANN, 1920 in The identity of Calliphara bipunctata, with proposal of a new synonymy (Hemiptera: Heteroptera: Scutelleridae)
Figures 4-9. Calliphara bipunctata LEHMANN, 1920, external male genitalia of lectotype. (4) Genital capsule, dorsal view; (5) same, lateral view; (6) same, posterodorsal view; (7) phallus, dorsal view; (8) same, lateral view; (9) same, ventral view. Scales in mm. Lettering: aed = aedeagus; cp-I = first conjunctival process; cp-II 1, cp-II 2 = branches of second conjunctival process; cp-III 1, cp-III 2 = branches of third conjunctival process (L = left, R = right); dsp = dorsal setal patch; phtr = phallotreme; vsp = ventral setal patch. Arrow in fig. 5 shows aspect of fig. 6.
Figures 1-3. Calliphara bipunctata LEHMANN, 1920 in The identity of Calliphara bipunctata, with proposal of a new synonymy (Hemiptera: Heteroptera: Scutelleridae)
Figures 1-3. Calliphara bipunctata LEHMANN, 1920, Lectotype. (1) dorsal view; (2) ventral view; (3) labels. Scales in mm.
FIGURE 2 in Morphological and molecular evidence of Turkish Minuartiella species (Caryophyllaceae), with a desciption of a new species and a proposal for a new combination
FIGURE 2. Minuartiella serpentinicola: (A) habit, (B) cyme, (C) bract, (D) sepal, (E) petal, (F) gland, (G) capsule.
FIGURE 4 in Morphological and molecular evidence of Turkish Minuartiella species (Caryophyllaceae), with a desciption of a new species and a proposal for a new combination
FIGURE 4. SEM photographs of the seed coat. (A) Minuartiella serpentinicola, (B) M. pestalozzae. Scale bars: 200 mm (A1, and B1), 100 mm (A2, and B2), 10 mm (A3, and B3).
FIGURE 1 in Morphological and molecular evidence of Turkish Minuartiella species (Caryophyllaceae), with a desciption of a new species and a proposal for a new combination
FIGURE 1. Molecular phylogenetic reconstruction by maximum likelihood method based on ITS sequences showing the relationships of Minuartiella serpentinicola sp. nov. and other Minuartiella species.
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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.
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.