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Figs. 1–3. Javeta pallida. 1 in First Report of the Indian Date Palm Leaf Miner, Javeta pallida Baly (Coleoptera: Chrysomelidae: Cassidinae: Coelaenomenoderini), on Pygmy Date Palm, Phoenix roebelenii O'Brien (Arecaceae)
Figs. 1–3. Javeta pallida. 1) Adult; 2) Infestation on Phoenix roebelenii in Kerala, India; 3) Infested leaflets.
FIGURE 20 in First report and three new species of Amanayara (Orthoptera: Grylloidea) in Minas Gerais State, Brazil
FIGURE 20. Occurrence map of the Amanayara de Mello & Jacomini, 1994 species in Brazil Southeast.
FIGURE 19 in First report and three new species of Amanayara (Orthoptera: Grylloidea) in Minas Gerais State, Brazil
FIGURE 19. Comparison of the phallic complex of Amanayara species. A—Amanayara ribasi sp. nov., ventral, dorsal and lateral view (up to down); B—Amanayara bernardesi sp. nov., ventral, dorsal and lateral view (up to down); C— Amanayara helenae sp. nov. ventral, dorsal and lateral view (up to down); D—Amanayara jutinga (paratype), ventral, dorsal and lateral view (up to down) and E—Amanayara piuna (paratype), ventral, dorsal and lateral view (up to down).
Figs. 1–3. Microtheca ochroloma. 1 in First Report of the Yellowmargined Leaf Beetle, Microtheca ochroloma Stål, 1860 (Coleoptera: Chrysomelidae), in Pennsylvania
Figs. 1–3. Microtheca ochroloma. 1) First, second, and fourth instars, pupal chamber, and adult; 2) Eggs on an old napa cabbage leaf; 3) First instar feeding on an old napa cabbage leaf.
Fig. 1 in First Report ofCaryedes brasiliensis(Thunberg) (Coleoptera: Chrysomelidae: Bruchinae) Preying on Seeds ofDioclea violaceaMart. ex Benth. (Fabaceae) In Brazil
Fig. 1. Dioclea violacea seeds damaged by Caryedes brasiliensis. A) Dioclea violacea pod; B) Seeds damaged by adults; C) Perforation of the seed for larval penetration; D) C. brasiliensis and D. violacea seeds.
Fig. 1 in First Report ofPeltophorus adustus(Fall) (Coleoptera: Curculionidae: Baridinae) in Mexico, with Two New Host Associations
Fig. 1. Damage to Agave cupreata by Peltophorus adustus. A) Feeding damage to a boll by adults, B) Seeds damaged by larvae, C) Pupa inside seed, D–E) Emerging adults.
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano. in The genus Ramalina Acharius (Ascomycota, Lecanoromycetes, Ramalinaceae) in northern South America
FIGURE. Typical habitats of Ramalina species on northern South America. A. High paramo, Laguna Anteojos, Sierra Nevada de Merida, where grows on rocks R. anteojina at 4100 m. B. Sub-paramo (timberline), La Aguada, Sierra Nevada de Merida, 3100 m, where are found R. dictyota and R. reducta on shrubs. C. Andean cloud forest, La Victoria, Sierra Nevada de Merida where R. cochlearis, R. cumanensis and R. victoriana are found growing as epiphytes. D. Populations of R. usnea, R. morrocoyensis and R. paradisensis growing as epiphytes on mangroves and Suriana maritima at sea level, National Park Morrocoy, state Falcón; the latter two species are known only from this locality. E. Ramalina usnea is the only species of this genus reported from the Alto Orinoco, Amazonas, near La Esmeralda, 150 m, growing as corticolous in submontane forests, at the top of the picture the Cerro Duida. F. Xerophytic forests from the National Park Cerro Santa Ana, state Falcón, where Ramalina santanensis and R. microphylla are known only growing on soil and rocks at 200–400 m. Photos V. Marcano.
FIGURE 5 in A preliminary report of Gymnopus sect. Impudicae (Omphalotaceae) from China
FIGURE 5. Microscopic features of G. similis (GDGM 78308). a. Basidiospores, b. Basidioles, c. Cheilocystidia, d. Caulocystidia, e. Pileipellis terminal cells. Scale bars, a–c = 10 μm, d–e = 20 μm.
FIGURE 3 in A preliminary report of Gymnopus sect. Impudicae (Omphalotaceae) from China
FIGURE 3. Microscopic features of Gymnopus alliifoetidissimus (GDGM 76695, holotype!). a. Basidiospores, b. Basidia, c. Basidioles, d. Cheilocystidia, e. Caulocystidia, f. Pileipellis terminal cells (Rameales-structure). Scale bars = a–e = 10 μm, f = 20 μm.
FIGURE 3 in Three new host records of endophytic Neofusicoccum species reported from Dendrobium orchids
FIGURE 3. Neofusicoccum parvum (MFLUCC 14-0163). A–B. Colony on PDA (A. surface, B. reverse). C–G. Conidiomata on PDA. H. Conidiogenous cells with conidia. I. Conidiogenous cell with conidium stained with Congo red. J–M. Conidia (I, L, M stained with Congored). Scale bars: C= 200 μm, D=500 μm, H=20 μm, I–K =10 μm, L–M=5 μm.
FIGURE 2 in Three new host records of endophytic Neofusicoccum species reported from Dendrobium orchids
FIGURE 2. Neofusicoccum occulatum on PDA (MFLUCC 20-0234) A–B. Colony on PDA (A: surface, B: reverse). C. Conidiomata masses. D–G. Conidia. Scale bars: C=500 μm, D–G=10 μm.
FIGURE 4 in Three new host records of endophytic Neofusicoccum species reported from Dendrobium orchids
FIGURE 4. Neofusicoccum parvum (MFLUCC 19-0244, C–N from WA). A–B. Colony on PDA (A: surface, B: reverse). C. Conidiomata on slide culture. D–G. Pycnidia. H–L. Conidiogenous cells with conidia. M–N. Conidia. Scale bars: H=10 μm, I–J=5 μm, K–N=10 μm.
FIGURE 1. The consensus phylogram resulting from a in Three new host records of endophytic Neofusicoccum species reported from Dendrobium orchids
FIGURE 1. The consensus phylogram resulting from a RAxML analysis of the combined four loci alignment (ITS-RPB2 -EF-1α-TUB2) of the analysed Neofusicoccum and related species sequences. Strains isolated in this study are in red. Ex-epitype and ex-type isolates are
Figure S1. Autophagy inhibitors in the autophagy reporter THP1-Difluo hLC3 cell line
<p>Cells (5 ×10<sup>5</sup> cells/mL) were incubated with two concentrations of (<strong>a</strong>) mTOR activator MHY1485, (<strong>b</strong>) AMPK inhibitor dorsomorphin, (<strong>c</strong>) ULK1/2 inhibitor MRT68921, (<strong>d</strong>) PI3K class III inhibitor wortmannin, (<strong>e</strong>) autophagosome-lysosome fusion inhibitor chloroquine, and (<strong>f</strong>) late-stage autophagy inhibitor bafilomycin A1 for 24 h. Autophagic flux was determined by measuring the fluorescence of RFP and GFP. The ratio of median fluorescence intensity of RFP to GFP (MFI) was normalized (nMFI) to the vehicle control (CTRL DMSO). Data are means ±SEM of 4 independent experiments, each carried out in duplicate.</p>
Figure 5 in Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa, Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence
Figure 5. Photomicrographs of morphogenesis in Pseudoamphisiella elongata sp. nov. after protargol impregnation. A, middle part of cell, ventral view, showing the oral primordium for both dividers, and the undifferentiated parental structures; B, ventral view, arrows indicate the primary frontoventral–transverse (FVT) anlagen; C, ventral view of an early divider, arrowheads and arrows mark the left and right marginal row anlagen, respectively; D, a slightly later stage, note the merging of the macronuclear nodules, the arrow indicates the disaggregating of the old undulating membranes; E, ventral view of a middle-stage divider, arrows indicate the two migratory cirri derived from the last FVT cirral anlagen; F, middle portion of cell, ventral view, arrows mark the left marginal row anlagen in the opisthe; G, ventral view, arrows denote two migratory cirri derived from the last FVT cirral anlagen; H–J, ventral views of three specimens at slightly differing middle stages, the arrows in (H) and (J) indicate two migratory cirri derived from the last FVT cirral anlagen. Scale bars: 15 Mm in A; 50 Mm in C.
Figure 4 in Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa, Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence
Figure 4. Pseudoamphisiella elongata sp. nov. in the middle and late stages of morphogenesis, after protargol impregnation. A, B, ventral and dorsal views of the same specimen in the middle stage, showing the development of cirri and the single macronuclear mass; C, D, ventral and dorsal views of a late divider (same specimen), arrows indicate the differentiation of the extra anlagen, and arrowheads show the single caudal cirrus that develops from the posterior end of each dorsal kinety; E, ventral view of a late divider, note the newly built cirri; F, G, ventral and dorsal views of a very late divider, arrows indicate the newly formed extra right marginal cirri. Abbreviations: MVR, midventral row; RMR, right marginal row; TC, transverse cirri; UMA, undulating membrane anlagen. Scale bar: 60 Mm.
Figure 7. A in Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa, Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence
Figure 7. A, small subunit (SSU) rRNA gene sequence of Pseudoamphisiella elongata sp. nov. aligned with the sequences of Pseudoamphisiella alveolata, Pseudoamphisiella lacazei, and Pseudoamphisiella quadrinucleata. The numbers above the lines indicate the nucleotide numbers. The differences in sequence lengths were compensated for by introducing alignment gaps (–) in the sequences. Matched sites are marked with dots. B, phylogenetic tree of SSU rRNA sequences showing the positions of Pseudoamphisiella found with maximum-likelihood (ML) analysis, applying the GTR+G+I model. Species sequenced in the present study are shown in bold type. The numbers near branches are ML bootstrap values/Bayesian inference (BI) posterior probability values. The scale bar corresponds to five substitutions per 100 nucleotide positions.
Figure 2 in Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa, Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence
Figure 2. Photomicrographs of Pseudoamphisiella elongata sp. nov. from life (A–H) and after protargol impregnation (I–N). A–D, ventral views of different individuals, arrows mark the pellicular alveolus; E, lateral view, the inset shows part of the cortex, and the arrowheads indicate the rod-shaped extrusomes; F, portion of cortex (dorsolateral view), arrows indicate the extrusomes; G, outline shape of a stationary individual; H, dorsal view of cortex, showing the polygonalshaped alveoli; I, dorsal view, arrows mark the dorsal kineties; J, caudal portion, the arrow indicates the caudal cirri; K, middle portion of cell, ventral view, the arrow marks the end of the right midventral row; L, posterior end of body, ventral view, the arrows indicate the two fine pretransverse cirri that can be easily overlooked; M, anterior part of body, ventral view, arrows indicate the frontal cirri; N, ventral infraciliature. Scale bars: 100 Mm in A, B; 50 Mm in C, D, G, H.
Figure 6 in Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa, Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence
Figure 6. Photomicrographs of morphogenesis in Pseudoamphisiella elongata sp. nov. after protargol impregnation. A, ventral view, the arrow indicates the extra anlage adjacent to the right marginal row anlage; B, dorsal view, arrows denote the dorsal kineties anlagen; C, ventral view of opisthe in late stage, the arrow marks two buccal cirri; D, ventral view, arrowheads denote the pretransverse cirri; E–K, ventral views of middle to late stage dividers, showing the migration of all ciliary organelles and the division of the macronuclei; L, ventral view of a reorganizer at a late stage. Scale bars: 25 Mm in A; 60 Mm in E.
Figure 1 in Morphology and morphogenesis of a new marine hypotrichous ciliate (Protozoa, Ciliophora, Pseudoamphisiellidae), including a report on the small subunit rRNA gene sequence
Figure 1. Morphology of Pseudoamphisiella elongata sp. nov. from living observation (A–E) and after protargol impregnation (F–G). A, ventral view of a typical individual; B, ventral view of a slimmer individual; C, ventral view, note the ingested pennate diatoms; D, E, portion of cortex (top and side view), showing the polygonal-shaped alveoli and the rod-shaped extrusomes (arrows); F, ventral view of infraciliature, arrowheads indicate two fine pretransverse cirri; G, dorsal view of the same specimen as shown in (F), showing the macronuclear nodules, micronuclei, and dorsal kineties. Abbreviations: CC, caudal cirri; DK, dorsal kineties; EM, endoral membrane; FC, frontal cirri; LMR, left marginal row; Ma, macronucleus; Mi, micronucleus; MVR, midventral row; PM, paroral membrane; RMR, right marginal row; TC, transverse cirri. Scale bars: 50 Mm in A, B, C, F, G; 10 Mm in E.
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.