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Fig. 2 in Direction and timing of dispersal of Scirtothrips dorsalis (Thysanoptera: Thripidae) on select ornamental host plant species in south Florida
Fig. 2. Population estimates and dispersal of Scirtothrips dorsalis to 2 hosts at TREC, 19 Jul to 27 Sep 2007. (A) Mean weekly numbers of nymphs and pupae found on buttonwood foliage. (B) Mean weekly numbers of adults washed from plant terminals with data from buttonwood and schefflera pooled. (C) Mean weekly captures of adults on yellow sticky-card traps behind buttonwood and schefflera plants. Symbols represent means ± SD. An asterisk (*) indicates a significant difference from the other weeks according to 1-way ANOVAs and t-test comparisons at P ≤ 0.05. Mean weekly temperatures (T °C) and relative humidity (RH %) for the 3 mo period are shown parallel to the X-axis (FAWN 2007).
Fig. 1 in Direction and timing of dispersal of Scirtothrips dorsalis (Thysanoptera: Thripidae) on select ornamental host plant species in south Florida
Fig. 1. Experimental setups. (A) Population estimates and dispersal from rose to buttonwood and schefflera. Darkest grey represents rose, whereas the 2 lighter grey shades represent buttonwood or schefflera with the same shade of grey representing the same plant species. (B) Flight behavior during the day. Circles represent potted rose plants in 11 L containers. Small black rectangles denote locations of yellow sticky-card traps relative to each plot.
Fig. 3 in Direction and timing of dispersal of Scirtothrips dorsalis (Thysanoptera: Thripidae) on select ornamental host plant species in south Florida
Fig. 3. Population estimates and dispersal of Scirtothrips dorsalis to 2 hosts: cumulative data for the 11 wk test period. (A) Mean damage ratings on a scale of 0 to 5. (B) On-plant densities of S. dorsalis. (C) Weekly captures of adults on yellow sticky-card traps. (D) Weekly captures of adults on yellow sticky-card traps by cardinal direction of traps from plants. Symbols represent means ± SD. An asterisk (*) indicates a significant difference at P ≤ 0.05 (A–C) between host plant species according to t-tests or (D) from the other host plant pairs at other cardinal orientations based on a 1-way ANOVA followed by a Tukey–Kramer HSD test.
Text-fig. 4. A – Alasia sp., pollen ornamentation, compared with B – extant Quercus castaneifolia C.A. Mey (courtesy of Natalia Naryshkina, Institute of Biology and Soil Science, Vladivostok), with similar verrucate – scabrate elements. Scale bar 1 µm. in In Situ Pollen Of Alasia, A Supposed Staminate Inflorescence Of Trochodendroides Plant
Text-fig. 4. A – Alasia sp., pollen ornamentation, compared with B – extant Quercus castaneifolia C.A. Mey (courtesy of Natalia Naryshkina, Institute of Biology and Soil Science, Vladivostok), with similar verrucate – scabrate elements. Scale bar 1 µm.
Figure 2 in The phenology of Pulvinaria floccifera Westwood (Hemiptera: Coccomorpha: Coccidae) a new invasive pest on ornamentals outdoors in Poland
Figure 2. Life cycle of Pulvinaria floccifera Westwood on Ilex aquifolium outdoors in Poland in the years 2009 (), 2010 (), 2011 (), the period of maximum abundance (). Table. The dates of the first appearance of Pulvinaria floccifera Westwood instars in the years 2009–2011 and the number of days from hatching to each following stage.
Fig. 2 in Suitability of selected ornamental plants for growth and survival of Lissachatina fulica (Gastropoda: Achatinidae)
Fig. 2. Mean percent survival of newly hatched Lissachatina fulica afer 70 d of feeding on a single diet treatment. (A) Annual plants. (B) Perennial plants. Means topped by the same lowercase letters are not significantly different (P> 0.05; Kruskal-Wallis rank sum test and Dunn's test). Error bars indicate standard error.
Fig. 1 in Evaluation of reduced-risk insecticides to control chilli thrips (Thysanoptera: Thripidae) and conserve natural enemies on ornamental plants
Fig. 1. Mean percentage (± SEM) of Rhaphiolepsis indica foliage with Scirtothrips dorsalis feeding damage 42 days afer insecticide treatment. Different letters indicate significant differences between treatments using Tukey-Kramer HSD means comparison (P <0.05). Cyantraniliprole low (59.1 mL per 378.5 L) and cyantraniliprole high (236.6 mL per378.5 L).
Figure 2 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 2. - Neobythites bimarginatus. Pelvic-fin length and horizontal eye diameter showing negative allometric growth.
Figure 1 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 1. - Neobythites bimarginatus Fourmanoir & Rivaton, 1979. SAIAB 189024, SL 122 mm. From off Madagascar (photo M. Krag, ZMUC).
Fig. 2 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 2. Reconstruction of the skull of Spinops sternbergorum gen. et sp. nov. from the Campanian of Dinosaur Provincial Park, southern Alberta, in right lateral view. Preserved elements are stippled; missing portions are dotted and modeled after Centrosaurus apertus.
Fig. 6 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 6. Phylogenetic hypotheses for relationships within Ceratopsidae, focusing on Centrosaurinae. A. Strict reduced consensus tree using "traditional" codings for the epiparietal homologies in selected centrosaurines (see text), with Sinoceratops zhuchengensis and Rubeosaurus ovatus removed. B. Strict consensus tree using "new" codings for epiparietal homologies, following a posteriori deletion of Sinoceratops zhuchengensis and Centrosaurus brinkmani. At selected nodes, the top number indicates Bremer support and the bottom number indicates bootstrap support values above 50%.
Fig. 5 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 5. Schematized parietals of centrosaurine ceratopsids in dorsal view, showing possible homologies for the first four epiparietal loci. A. Albertaceratops nesmoi Ryan, 2007. B. Spinops sternbergorum gen. et sp. nov. C. Centrosaurus apertus Lambe, 1902. D. Styracosaurus albertensis Lambe, 1913. E. Rubeosaurus ovatus Gilmore, 1930. F. Einiosaurus procurvicornus Sampson, 1995. Numbers indicate locus positions. For A and B, the numbers on the right side of the parietal indicate numbering under the "traditional" scheme; numbers on the left side indicate numbering under the revised scheme proposed here. Locus numbering is the same in both the traditional and revised schemes for C, D, E, and F, and are thus presented only on the left side of the parietal for those taxa. Not to scale.
Fig. 4 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 4. Partial skull of the centrosaurine ceratopsid Spinops sternbergorum gen. et sp. nov. from the Campanian of Dinosaur Provincial Park, southern Alberta, NHMUK R16306; in right lateral (A), rostral (B), and dorsal (C) views.
Fig. 3 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 3. Centrosaurine ceratopsid Spinops sternbergorum gen. et sp. nov. from the Campanian of Dinosaur Provincial Park, southern Alberta. A. Partial right squamosal in lateral view, NHMUK R16309. B. Partial parietal with adherent bone fragments in dorsal view, NHMUK R16308. C. Partial parietal in dorsal (C1), rostral (C2), and left lateral (C3) views, holotype NHMUK R16307.
Fig. 1 in A new centrosaurine from the Late Cretaceous of Alberta, Canada, and the evolution of parietal ornamentation in horned dinosaurs
Fig. 1. Map showing the presumed location of the Spinops sternbergorum gen. et sp. nov. type locality within the area informally called the "Steveville badlands," Dinosaur Provincial Park, Alberta Canada. Charles Sternberg (unpublished data in NHMUK archives) indicated that the bone bed was one mile below the mouth of Berry Creek, and the estimated area that this covers is indicated by the grey semi−circle. Intense prospecting on the east side of the river has failed to relocate the quarry, and badlands on the west side are outside of the Park boundary and currently inaccessible for prospecting. The indicated southeast Park boundary does not include the margins of two major coulees in this region that are also within the Park. Note that the quarry for the holotype of Styracosaurus albertensis Lambe, 1913 (CMN 344) is in the southeast part of the Park. The inset photograph, courtesy of David Eberth, shows a typical view of the contact between the Dinosaur Park Formation (DPF) and Oldman Formation (OF) near the Steveville badlands.
FIGURE 3 in Diversity of Loricariidae (Actinopterygii: Siluriformes) assemblages in two Conservation Areas of the Middle Xingu River, Brazilian Amazon, and their suitability for sustainable ornamental fisheries
FIGURE 3 | Principal component analysis (PCA) for composition of ornamental fish species based on the method of capture (Hellinger transformation), considering the two extractive reserves.
FIGURE 4 in Diversity of Loricariidae (Actinopterygii: Siluriformes) assemblages in two Conservation Areas of the Middle Xingu River, Brazilian Amazon, and their suitability for sustainable ornamental fisheries
FIGURE 4 | Principal Component Analysis (PCA) of fish composition in the drainages of both the Xingu and Iriri River RESEXes (Hellinger transformation). Only species names that made greatest contributions to compositional differences are shown.
FIGURE 2 in Diversity of Loricariidae (Actinopterygii: Siluriformes) assemblages in two Conservation Areas of the Middle Xingu River, Brazilian Amazon, and their suitability for sustainable ornamental fisheries
FIGURE 2 | Venn diagram showing the compositions of the Loricariidae species found in both extractive reserves.
Figure 31. - Alveolar ornamentation type. A in Guide for the identification of archaeological sea sturgeon (Acipenser sturio and A. oxyrinchus) remains
Figure 31. - Alveolar ornamentation type. A: Alveolar pattern with tubercular characteristics at the edge in A. oxyrinchus (NRM 60821, 4th dorsal scute, 99 cm TL); B: Alveolar pattern in a large A. oxyrinchus (MHNNZ 19558, 6th left lateral scute, 276 cm TL); C: Lacrimale-suborbitale from Trigla lucerna (RBINS 23663; 47.5 cm SL). Note the alveolar-like ornamentation. Scale bars = 1 cm.
Fig. 2 in Effect of common ornamental plants on the survivorship and fecundity of the Aedes albopictus (Diptera: Culicidae)
Fig. 2. Survival curves of male (A, C, E) and female (B, D, F) Aedes albopictus exposed to different plant species, 10% sucrose, or water only. A and B refer to control groups; C and D refer to flowering plants; E and F refer to nonflowering plants.
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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.