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Figs 10–19 in Two New Species of Unilobus Théodoridès, Desportes and Jolivet, 1984 (Apicomplexa: Conoidasida) Parasitizing Tenebrionid Beetles along with the Remarks on the Genus and Its Family Status
Figs 10–19. Camera lucida drawings of different stages of life cycle of Unilobus scleroni n. sp. 10 – early development of parasite in the epithelial tissue, showing that the development is intracellular; 11 – early gamont attached to the epithelial cells; 12 – gamont in section; 13–15 – gamonts of different ages, showing the position of the nucleus; 16 – gamont in caudo-frontal association; 17 – dehiscence of gametocyst; 18 – gametocyst with fully formed nine sporoducts; 19 – oocysts (= spores) in chain.
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass]. in Isolated Ossicles Of The Family Eospondylidae Spencer Wright, 1966, In The Lower Devonian Of Bohemia (Czech Republic) And Correction Of The Systematic Position Of Eospondylid Brittlestars (Echinodermata: Ophiuroidea: Oegophiurida)
Text-fig. 2. Eospondylus primigenius (STÜRTZ) Bundenbach, Eschenbach-Bocksberg quarry, Lower Devonian, Lower Emsian (Zlichovian), Hunsrück Slate,, NM S 4764, x 3. Specimen with ventral arm coiling. The specimen is on its dorsum in slate with all five rays curled ventrally inward toward mouth area on underside of disk. Barely visible are tips of two jaws; slightly exposed are proximal parts of rays in oral view extending outward from disk. The location of abrupt ventral bending of rays is indicated by emergence from slate of five rays in aboral view that point inward toward buried disk. Based on ventral bending of rays and intimate association with crinoids Eospondylus has been interpreted as stratigraphic first occurrence of Order Euryalida, which contains epizoic gorgonocephalid and euryalid basket-stars of modern oceans. This status is rejected using new evidence from isolated vertebrae. [Photo by Alexander Glass].
Text-fig. 1. Map of the Za Hájovnou Cave with Section Nos. 1 and 2 (surveyed by M. Vaněk, status in 2005). in New Updated Results Of Paleomagnetic Dating Of Cave Deposits Exposed In Za Hájovnou Cave, Javoříčko Karst
Text-fig. 1. Map of the Za Hájovnou Cave with Section Nos. 1 and 2 (surveyed by M. Vaněk, status in 2005).
Figure 4 in DNA barcoding and a new taxonomic status of the Triaenodes ochreellus lefkas Malicky, 1974 (Insecta, Trichoptera) with new distribution data
Figure 4. Distribution of Triaenodes ochreellus ochreellus (green field) and Triaenodes ochreellus lefkas (blue field) with new data in Albania, Croatia and Montenegro (red points).
Figure 3 in DNA barcoding and a new taxonomic status of the Triaenodes ochreellus lefkas Malicky, 1974 (Insecta, Trichoptera) with new distribution data
Figure 3. Maximum likelihood (Ml) phylogram based on the 658 bp long fragment of the DNA barcode region showing the relationships among the species of the genus Triaenodes. Numbers above the branches represent bootstrap support (bs) for Neighbor-Joining (NJ) and Ml analysis (NJ/Ml). BS values less than 70 are not shown. The groups delineated by Automatic Barcode Gap Discovery (ABGD) approach are shown on the right side of the tree.
Fig. 9 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 9. Plot of principal component scores for continuous characters for L. balagueri (yellow stars, n = 12), L. chiribaya (purple circles, n = 10), L. insolitus (red triangles, n = 15), L. nazca (sky blue triangle, n = 7), and L. anqapuka sp. nov. (green squares, n = 7). Eigenvectors, eigenvalues, and percent of variation explained for the first two principal components are summarized in Table 5.
Fig. 7 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 7. Habitat of Liolaemus anqapuka sp. nov. in (A) dry season and (B) wet season. Photos by A. Quiroz (A), C.S. Abdala (B).
Fig. 2 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 2. Details of the holotype of Liolaemus anqapuka sp. nov. (MUSA 5573; SVL = 73.5 mm, Tail = 63.9 mm): (A) dorsal and (B) ventral views of body; (C) ventral, (D) dorsal, and (E) lateral views of head; (F) ventral view of precloacal pores. Scale = 10 mm.
Fig. 4 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 4. Male specimens of the Liolaemus anqapuka sp. nov. Photos by A. Quiroz (A–D) and C.S. Abdala (E).
Fig. 6 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 6. Geographic distribution of Liolaemus montanus group species from Peru. Symbols with a black dot in the middle represent the type locality of each species. Species with quotation marks in the names belong to the candidate species listed in Aguilar et al. (2016).
Fig. 1 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 1. Biogeographic regionalization proposed by Morrone (2014), showing the limits of the Desert province and Atacama province. The geoform La Caldera batholith, adapted from Ramos (2008), is also shown.
Fig. 3 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 3. Adult male of the holotype, Liolaemus anqapuka sp. nov. (MUSA 5573; SVL = 73.5 mm, Tail = 63.9 mm), from the Department of Arequipa, 2,460 m asl. Photos by C.S. Abdala.
Fig. 11 in Some color in the desert: description of a new species of Liolaemus (Iguania: Liolaemidae) from southern Peru, and its conservation status
Fig. 11. Phylogenetic trees showing the relationships between Liolaemus anqapuka sp. nov. and species within the L. montanus group by (A) Total Evidence analysis, (B) molecular phylogenetic analysis, and (C) morphological phylogenetic analysis. The values correspond to the support measure with symmetric resampling.
Fig 3 in Avifaunal status updates, range extensions and potential new taxa on the lesser Sangihe and Talaud islands, Indonesia
Fig 3. Island Whistler (Pachycephala phaionota). A, Individual 1, Karatung, 30 June 2016; B, Individual 2, Marampit, 26 June 2016; C, Individual 3, 26 June 2016; D, Nest and egg of individual 3, Marampit, 26 June 2016.
Fig. 1 in Avifaunal status updates, range extensions and potential new taxa on the lesser Sangihe and Talaud islands, Indonesia
Fig. 1. Map of the Sangihe and Talaud islands, also showing the surrounding landmasses (top-left) and the Nanusa islands (bottom-right). Based on satellite imagery from Google (2017).
Figure 7 in YELLOW WATER LILIES (NUPHAR, NYMPHAEACEAE) IN GREAT BRITAIN: A NEW HYBRID, A REAPPRAISAL OF RECORDS, AND A REVISED STATUS OF N. ADVENA
Figure 7. Sepals of: A, Nuphar advena from NA1 population, Spottiswoode Loch; B, Nuphar × porphyranthera from NH8 population, Oulten Park (left), and NH2 population, Godstone (right); C, N. lutea (no population code), Norbotten, Sweden. Scale bars are approximate (no measurements of the photographed features were taken). Photographs: R. V. Lansdown.
Figure 6. A in YELLOW WATER LILIES (NUPHAR, NYMPHAEACEAE) IN GREAT BRITAIN: A NEW HYBRID, A REAPPRAISAL OF RECORDS, AND A REVISED STATUS OF N. ADVENA
Figure 6. A, Petiole shape of Nuphar advena from NA1 population, Spottiswoode Loch. B, Petiole shape of Nuphar × porphyranthera from NH8 population, Oulten Park (left); NH6 population, Shropham Ponds (centre); and NH1 population, West Hoathly (right). C, Petiole shape of Nuphar lutea (no population code), Elterwater. Scale bars are approximate (no measurements of the photographed features were taken). Photographs: R. V. Lansdown.
Figure 4 in YELLOW WATER LILIES (NUPHAR, NYMPHAEACEAE) IN GREAT BRITAIN: A NEW HYBRID, A REAPPRAISAL OF RECORDS, AND A REVISED STATUS OF N. ADVENA
Figure 4. Habit of Nuphar × porphyranthera, showing decaying leaves in July 2020, from NH4 population, Painshill Park. Photograph: R. V. Lansdown.
Figure 2. A in YELLOW WATER LILIES (NUPHAR, NYMPHAEACEAE) IN GREAT BRITAIN: A NEW HYBRID, A REAPPRAISAL OF RECORDS, AND A REVISED STATUS OF N. ADVENA
Figure 2. A, Flower of Nuphar × porphyranthera with some stamens removed, from NH8 population, Oulton Park, June 2021. B, Sterile stamens of Nuphar × porphyranthera: filament length (fl), anther length (al). C, Fertile stamens of Nuphar advena. Scale bars are approximate (no measurements of the photographed features were taken). Photographs: R. V. Lansdown.
Figure 3 in YELLOW WATER LILIES (NUPHAR, NYMPHAEACEAE) IN GREAT BRITAIN: A NEW HYBRID, A REAPPRAISAL OF RECORDS, AND A REVISED STATUS OF N. ADVENA
Figure 3. Anther and filament lengths of Nuphar lutea (n = 30 from 3 populations), N. advena (n = 10 from 1 population) and their hybrid Nuphar × porphyranthera (n = 100 from 10 populations).
ScienceDex guides
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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.