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FIGURE 5. Deamia. A in A phylogenetic framework for the Hylocereeae (Cactaceae) and implications for the circumscription of the genera
FIGURE 5. Deamia. A) D. chontalensis in habitat (M. Yañez 04); B) D. chontalensis, stem (M. Yañez 05); C) D. testudo, flower (M. Yañez 02) (photos by S. Arias).
FIGURE 1 in A phylogenetic framework for the Hylocereeae (Cactaceae) and implications for the circumscription of the genera
FIGURE 1. Stem and flower morphology of the Hylocereeae. A) Acanthocereus chiapensis (Arias 1021); B) A. tetragonus (Arias 2166); C) Disocactus quezaltecus (Veliz 42515); D) D. phyllanthoides (Arias 1432); E) Aporocactus flagelliformis (Arias 1236); F) Epiphyllum cartagense (Hammel 19793); G) E. chrysocardium (cultivated, Botanical Garden UNAM); H) E. hookeri subsp. hookeri (Arias 1560); I) E. thomasianum (Hammel 22020); J) Pseudorhipsalis himantoclada (Hammel 20806); K) P. ramulosa (Ferrufino 718); L) Hylocereus monacanthus (Hammel 26600); M) H. undatus (cultivated, Botanical Garden UNAM); N) Selenicereus anthonyanus (Hammel, cultivated); O) S. dorschianus (Arias 2221); P) S. pteranthus (Garcia 874); Q) Weberocereus glaber (Bravo s.n.) [photos by S. Arias (A–H, K, M, O–Q), and B. Hammel (I, J, L, N)].
FIGURE 4. Strophocactus. A in A phylogenetic framework for the Hylocereeae (Cactaceae) and implications for the circumscription of the genera
FIGURE 4. Strophocactus. A) S. wittii, flowering specimen (Schmidt s.n., cultivated at the Botanic Garden Bonn). B) Strophocactus wittii (left) and Strophocactus (Pseudoacanthocereus) sicariguensis (right), both forming flattened stems [photos by W. Barthlott, LotusSalvinia.de].
FIGURE 3 in A phylogenetic framework for the Hylocereeae (Cactaceae) and implications for the circumscription of the genera
FIGURE 3. Convergent fern-like flattened stems in A) Epiphyllum chrysocardium, B) Weberocereus imitans, C) Epiphyllum anguliger, D) Selenicereus (Cryptocereus) anthonyanus (photos by W. Barthlott, Lotus-Salvinia.de).
FIGURE 3. Fruits and a in Typification of the Linnaean name Corispermum squarrosum, with notes on C. hyssopifolium and nomenclatural implications for Agriophyllum (Chenopodiaceae: Corispermeae)
FIGURE 3. Fruits and a bract of the specimen LINN 12.3 (lectotype of Corispermum squarrosum L., here designated).
FIGURE 2 in Typification of the Linnaean name Corispermum squarrosum, with notes on C. hyssopifolium and nomenclatural implications for Agriophyllum (Chenopodiaceae: Corispermeae)
FIGURE 2. Fruits of the specimen LINN 12.2 (filed as Corispermum hyssopifolium L.), right-side plant. Taxonomic identity: Corispermum marschallii Steven.
FIGURE 3. Potential euglenophyte flagship species. A. Colacium epiphyticum. B. Trachelomonas hemisphaerica. C. Colacium minimum. D. Trachelomonas argentinensis. E. Trachelomonas magdaleniana. F. Phacus plicatus. G in African Trachelomonas saccasii found in a European mesotrophic pond (Czech Republic). Implication for euglenoid biogeography and recommendations for euglenoid flagship species
FIGURE 3. Potential euglenophyte flagship species. A. Colacium epiphyticum. B. Trachelomonas hemisphaerica. C. Colacium minimum. D. Trachelomonas argentinensis. E. Trachelomonas magdaleniana. F. Phacus plicatus. G. Lepocinclis crassicollis. Size ratio is not retained.
FIGURE 2 in African Trachelomonas saccasii found in a European mesotrophic pond (Czech Republic). Implication for euglenoid biogeography and recommendations for euglenoid flagship species
FIGURE 2. Visualization of Trachelomonas saccasii lorica using scanning electron microscopy. A. Lorica contain irregularly distributed pores. B. Detailed view of the lorica surface structure with several granules (indicated by arrows). C. Detailed view of the apical pore with a thickened edge (indicated by arrow).
FIGURE 1 in African Trachelomonas saccasii found in a European mesotrophic pond (Czech Republic). Implication for euglenoid biogeography and recommendations for euglenoid flagship species
FIGURE 1. Trachelomonas saccasii observed by light optical microscopy. A, B. General view of the lorica with thickening around the apical pore (marked with arrows) and several chloroplasts (some marked "Ch"). C. Lorica surface structure with irregularly distributed pores.
FIGURE 6 in Liu, H.J., Ding, C.H., He, J., Cheng, J., Pei, L.Y. & Xie, L. (2018) Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications. Phytotaxa 343 (3): 214-226.
FIGURE 6. Phylogeny of Clematis s.l. species inferred from complete chloroplast genome sequences. Bayesian phylograms are shown with MP bootstrap values/PP values at each node.
FIGURE 4 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 4. Sliding window analysis of the whole plastid genomes of eight Clematis s.l. samples. Lines parallel to the x-axis show the positions of the LSC, SSC, and IR regions. The vertical blue line shows the value of nucleotide diversity (Pi) in a sliding window analysis of window size 600 bp with step size 50 bp. The value is inserted at its mid-point.
FIGURE 3 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 3. Sequence alignment of eight plastomes of Clematis s.l. in the mVISTA program. Clematis terniflora was used as a reference. A cut-off of 70% similarity was used for the plot. The Y-scale represents the percent similarity (50–100%). Blue represents coding regions, and pink represents non-coding regions.
FIGURE 1 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 1. Map of the chloroplast genomes of Clematis s.l. Genes shown outside the circle are transcribed clockwise, whereas those inside the circle are transcribed counterclockwise. Genes belonging to different functional groups are colored. The dashed area in the inner circle indicates the GC content of the plastomes.
FIGURE 5 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 5. Analyses of repeated sequences in Clematis s.l. chloroplast genomes. A: Number of each repeat type; B: frequency of direct repeats by length; C: frequency of reverse repeats by length; D: frequency of palindromic repeats by length; E: location of repeats.
FIGURE 2 in Complete chloroplast genomes of Archiclematis, Naravelia and Clematis (Ranunculaceae), and their phylogenetic implications
FIGURE 2. Comparison of the LSC, IRs and SSC borders among Clematis s.l. samples used in this study.
Understanding the Implications of Changes to Build Systems (Replication Package)
<p>Online appendix for <em>"Understanding the Implications of Changes to Build</em> Systems", in the Proceedings of the International Conference on Software Engineering (ICSE), 2023. </p>
Figure 2 in Density, occupancy and detectability of tortoise species (Chelonoidis spp.) in the Atlantic Forest: implications for conservation and management
Figure 2. Relationship between the probability of detection of Chelonoidis denticulatus (A) and Chelonoidis carbonarius (B) with the accumulated rainfall of the day before sampling (previous rainfall) in the Vale Natural Reserve, Brazil.
Figure 1 in Density, occupancy and detectability of tortoise species (Chelonoidis spp.) in the Atlantic Forest: implications for conservation and management
Figure 1. Location of the Vale Natural Reserve, municipality of Linhares, Espírito Santo, south-eastern Brazil, showing the location of the linear transects and the types of vegetation present in the Reserve.
Figure 3 in Density, occupancy and detectability of tortoise species (Chelonoidis spp.) in the Atlantic Forest: implications for conservation and management
Figure 3. Relationship between the probability of occupancy of Chelonoidis denticulatus (A) and Chelonoidis carbonarius (B) with the distance from the water resource, and relationship between the probability of occupancy of Chelonoidis denticulatus and the percentage of forest cover (C) in the Vale Natural Reserve, Brazil.
FIGURE 2 in The original description of Agama gutturosa Merrem, 1819 and its nomenclatural implication on the genus Bronchocela Kaup, 1827 (Squamata: Agamidae)
FIGURE 2. Bronchocela jubata (ZMB 686, von Borcke's specimen). Upper panel: lateral view. Lower panel: ventral view. Please note the unnaturally formed gular region.
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.