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Figure 6 in Molecular characterization and protective efficacy of a new conserved hypothetical protein of Eimeria tenella
Figure 6. Localization of EtCHP18905 in infected DF-1 cells by indirect immunofluorescence. Parasites incubated with anti-rEtCHP18905, stained with FITC (green)-conjugated secondary antibodies, and counterstained with DAPI (blue). Infected DF-1 cells were collected at indicated time points post-infection. (A) Sporozoites (Spz) in PBS, pRB, posterior refractile body; (B) Spz in complete medium. Infected DF-1 cells were collected at the indicated time points post-infection (pi); (C) 2 hours pi (hpi); (D) immature schizonts (iSC) 48 hpi; (E) mature schizonts (mSC) 72 hpi; (F) merozoites (Mrz) in PBS.
Figure 6 in Further investigation of the characteristics and biological function of Eimeria tenella apical membrane antigen 1
Figure 6. KEGG pathway classification of differentially expressed proteins in DF-1 cells transiently transfected with EtAMA1.
Figure 6 in Sheltered life beneath elytra: three new species of Eutarsopolipus (Acari, Heterostigmatina, Podapolipidae) parasitizing Australian ground beetles
Figure 6. Phase-contrast micrograph of tarsus III in Eutarsopolipus pulcher n. sp. (adult female) representing modified trifurcate seta uļ and spur-like seta tcļļ.
Figures 1–6 in Morphological updates and molecular description of Heterosentis holospinus Amin, Heckmann, & Ha, 2011 (Acanthocephala, Arhythmacanthidae) in the Pacific Ocean off Vietnam
Figures 1–6. SEM of specimens of Heterosentis holospinus from Leiognathus equulus from Vietnam. (1) The anterior part of a worm showing the proboscis, the spineless anterior trunk cone, and the anterior part of the spiny trunk. (2) A longitudinal Gallium cut section of the anterior hook. Note the thickness of the hook layers and the relationship between the hook and the size and shape of the root. (3) Posterior hooks of the proboscis. (4) A general view of trunk spines and their pattern of distribution. (5) A high magnification of a typical duck-billshaped trunk spine showing a continuation of trunk micropores. (6) Micropores in a mid-section of the trunk.
Figure 6 in New species and new records of camallanid nematodes (Nematoda, Camallanidae) from marine fishes and sea snakes in New Caledonia
Figure 6. Procamallanus (Spirocamallanus) hexophtalmatis n. sp., scanning electron micrographs. (A, B) Cephalic end of female, sublateral and apical views, respectively; (C) posterior end of male, sublateral view; (D) posterior portion of male tail, lateral view (arrow indicates postanal papilla); (E) distal end of tail of first-stage larva; (F) digital appendages on tail tip of first-stage larva; (G) deirid. (a) amphid; (b) cephalic papilla of external circle; (c) cephalic papilla of middle circle; (d) cephalic papilla of internal circle; (p) phasmid.
Figure 6 in Phlebotomus (Paraphlebotomus) chabaudi and Phlebotomus riouxi: closely related species or synonyms?
Figure 6. Phylogenetic tree inferred by concatenation of the three loci under study. The phylogram was obtained by a partitioned ML analysis with a GTR (general time reversible) + G (gamma distribution of rates with four rate categories) + I (proportion of invariant sites) model using RAxML software [39]. The tree was visualized using the TreeDyn program, version 198.3 [7]. The percentages above the branches are the frequencies with which a given branch appeared in 500 bootstrap replications. Only bootstrap values higher than 50% on branches are shown. Concatenated sequences of Ph. sergenti were used as the outgroup.
Figure 6. Indopolystoma elongatum n. gen. n in Indopolystoma n. gen. (Monogenea, Polystomatidae) with the description of three new species and reassignment of eight known Polystoma species from Asian frogs (Anura, Rhacophoridae)
Figure 6. Indopolystoma elongatum n. gen. n. sp. from Zhangixalus arboreus. Hamuli and marginal hooklets from holotype and paratypes. (A–A') Holotype; (A''–A''') Paratypes; (B) Marginal hooklet C1; (B') Marginal hooklet C3; (B'') Marginal hooklet C8. Scale bar: 100 µm (A–A'''), 20 µm (B–B'').
Figure 6 in Application of the NucliSENS easyMAG system for nucleic acid extraction: optimization of DNA extraction for molecular diagnosis of parasitic and fungal diseases
Figure 6. Influence of the quantity of human cells (THP1 cells) on Leishmania quantification at various concentrations of host cells and parasites.
Figure 6 in The distribution, specimens and status of Chestnut Owlet Glaucidium (capense) castaneum and Albertine Owlet G. (c.) albertinum
Figure 6. Tail length plotted against length of folded wing for specimens of the different taxa in the African Barred Owlet Glaucidium capense complex.
Figure 6 in The taxonomic status of Crimson-crested Turaco Menelikornis (leucotis) donaldsoni
Figure 6. Left White-cheeked Turaco Menelikornis (l.) leucotis at Yergalem, south of Awasa, and right Crimsoncrested Turaco M. (l.) donaldsoni at Goro Gutu, west of Harar; here only minor differences in the size of the cheek patches and peri-ocular wattles are apparent (© Volker Sthamer)
Figure 6 in Specimens of the extinct Spectacled Cormorant Urile perspicillatus
Figure 6 (left and below). Detailed photographs of Spectacled Cormorant Urile perspicillatus skull and mandible in the collection of the Zoological Institute of the Russian Academy of Sciences, St Petersburg (ZISP 1112) (© V. Vysotsky)
Figure 6 in Fregetta lineata (Peale, 1848) is a valid extant species endemic to New Caledonia
Figure 6. Comparative measurements of New Caledonian Storm Petrel Fregetta lineata (black), White-bellied Storm Petrel F. grallaria (red) and Black-bellied Storm Petrel F. tropica (green). Data are presented as a correlation matrix for each pair of morphometric variables, with the diagonal in the matrix showing the distribution of each variable per taxon. Colour chart as in Fig. 4F.
Figure 6 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 6. The effect of narrow row spacing (<76 cm) on crop yield as explained by subgroups of the crop, tillage, weed type, weed management method, herbicide application frequency, and time. The vertical black dashed line indicates zero effect. The black dots represent mean effect sizes (log of response ratios [lnðRRÞ]) for each subgroup, and the black lines represent their respective 99% confidence intervals (CIs). The numbers in parentheses indicate the number of observations followed by the number of studies for each effect size. The effect sizes were considered significantly different when their 99% CIs did not overlap or contain zero.
Figure 6 in Recruitment biology of cleavers (GOlium spp.) populations in western Canada
Figure 6. Emergence percentage of Canadian Galium spp. populations in fall of (A) 2013 and (B) 2014. Error bars represent SE, and similar letters indicate values do not differ statistically at P = 0.05. SPG, Saskatchewan Pulse Growers.
Figure 6 in Environmental cues affecting horseweed (ConyzO cOnOdensis) growth types and their sensitivity to glyphosate
Figure 6. Biomass of upright and rosette Conyza canadensis plants of a susceptible population (S-117) in response to applications of glyphosate.
Figure 6 in Dynamics of arbuscular mycorrhizal fungi in relation to root colonization, spore density, and soil properties among different spreading stages of the exotic plant threeflower beggarweed (Desmodium triflorum) in a ZoysiO tenuifoliO lawn
Figure 6. Conceptual framework demonstrating possible mechanisms of soil arbuscular mycorrhizal fungi (AMF) during the spreading process of Desmodium triflorum in the Zoysia tenuifolia lawn. Numbers 1, 2, 3, and 4 indicate different spreading stages of the invasive plant D. triflorum. Corresponding mycorrhizal structures were shown as the four microscopic views. Light-green and medium-yellow circles indicate AM fungal spores predominantly produced by the root mycorrhizal structures of Z. tenuifolia and D. triflorum, respectively. Medium-green and dark-yellow lines indicate the life cycle of spores in Z. tenuifolia plants and in D. triflorum plants, respectively. The AM fungi might influence the spread of D. triflorum by the following steps: (1) the early stage of the lawn's development with only Z. tenuifolia growing but without D. triflorum present. This occurs at the very beginning of the lawn establishment, and the AM fungal spores that previously existed in the lawn soil first infected the fine roots of Z. tenuifolia and completed the life cycle on their own. (2) The early spreading stage of D. triflorum (level 1). The roots of the two plants come into contact with each other, inducing the external hyphae that originally grow closely on the Z. tenuifolia roots to infect the roots of D. triflorum. The difference between the mycorrhizal infections of the two host plants contributes to higher root mycorrhizal colonizations of D. triflorum compared with Z.tenuifolia. However, at this stage,D. triflorum is not as competitive as Z. tenuifolia in the lawn, although it has advantages in terms of mycorrhizal infections. Therefore, the soil AM fungal spores are still predominantly produced by the mycorrhizal structures of the AMF-infected Z. tenuifolia roots. (3) The intermediate spreading stage of D. triflorum (levels 2 and 3). Desmodium triflorum continues to spread in the lawn. The contact of the two plants becomes more frequent and further induces a much closer relationship between the AM infections of the two plants. The increased D. triflorum plants in the lawn and the advantage of D. triflorum in root mycorrhizal infections facilitate the contribution of the mycorrhizal structures of the D. triflorum roots to sporulation. Thus, in this stage, the soil AM fungal spores were produced by the mycorrhizal structures of both plants, thereby inducing insignificant correlations between the spore densities and the root colonizations of either Z. tenuifolia or D. triflorum. (4) The late spreading stage of D. triflorum (levels 4 and 5). Desmodium triflorum is dominant in the lawn.The large numbers of D. triflorum plants and the AM infection advantage of D. triflorum facilitate AMF sporulation in the soil, thereby inducing significant correlations between the spore densities and the root colonizations of D. triflorum. At the different spreading stages of D. triflorum, the soil AM fungal communities also change as a result of the changed contributions of the AMF-infected host plants to the sporulation.
Figure 6 in Shade avoidance cues reduce Beto vulgoris growth
Figure 6. Effect of reflected light from grass on sugar beet leaf number in 2015 greenhouse study, Laramie,WY.Regression equation and parameter estimates are provided in Table 2.
Figure 6 in Glufosinate enhances the activity of protoporphyrinogen oxidase inhibitors
Figure 6. Saflufenacil (Saflu) at 1 g ha−1 can overcome the lack of efficacy by glufosinate (Gluf) at 280 g ha−1 on Amaranthus palmeri under low temperature and humidity. Visual injury provided with glufosinate + saflufenacil compared with the two herbicides applied individually at high (A) and low (B) temperature and humidity.Means with the same letter do not differ according to Tukey's test (P <0.05). Error bars represent the standard deviations of the means.
Figure 6 in Pericarp-mediated chemical dormancy controls the fruit germination of the invasive hoary cress (Lepidium drobo), but not of hairy whitetop (Lepidium oppelionum)
Figure 6. The effect of treatment with abscisic acid (ABA), wash water from fresh pericarp, wash water of washed fresh pericarp, and wash water of afterripened pericarp on the germination kinetics of Lepidium drobo isolated seeds. (A) The effect of wash water from L. drobo pericarp on the germination of L. drobo fresh seeds. (B) Germination dose response of L. drobo fresh seeds incubated with different ABA concentrations applied. (C) The effect of wash water from L. drobo pericarp on the germination of L. drobo afterripened seeds. (D) Germination dose response of L. drobo afterripened seeds incubated with different ABA concentrations applied. Mean values ± SE (N = 3 × 25) of accessions KM 1296 and KM 1754 (2014 to 2015 harvest) at optimal germination assay conditions (12/12-h light regime at 25/15 C day/night for 28 d) are presented. Pericarp tissues weighing 300 mg were washed with 3 ml of distilled water using a shaker at 100 rpm for 6 h to obtain the pericarp wash water applied in the germination assays.
Figure 6 in Seedbank Persistence of Palmer Amaranth (Amoronthus polmeri) and Waterhemp (Amoronthus tuberculotus) across Diverse Geographical Regions in the United States
Figure 6. Interaction of experimental site by burial depth on percentage seed damage and loss averaged across 2014–2016 for Amoronthus polmeri and Amoronthus tuberculotus. Damaged seeds include broken, shrunk, or malformed seeds and those lost due to deterioration or futile germination, which were impossible to count. Vertical bars represent ± standard error of the mean. Supplemental information is also provided in Supplementary Tables S1 and S2, where the actual values averaged across three replications per treatment and five locations of seed material origins are shown.
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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.