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Fig. 2 in Severe attacks caused by Macrolenes dentipes (Olivier) on Feijoa, Acca sellowiana (O. Berg) Burret (Myrtaceae) in Italy (Coleoptera: Chrysomelidae)
Fig. 2 – Macrolenes dentipes (Olivier). Calabria, Borgia, 10.VI.2020. Percentage of leaf damage for each range.
Fig. 1 in Severe attacks caused by Macrolenes dentipes (Olivier) on Feijoa, Acca sellowiana (O. Berg) Burret (Myrtaceae) in Italy (Coleoptera: Chrysomelidae)
Fig. 1 – Adults of Macrolenes dentipes (Olivier) on Feijoa with damaged leaves. Calabria, Borgia, 29.V.2021.
Fig. 3 in Feeding behavior of Diaphorina citri (Hemiptera: Liviidae) and its acquisition of 'Candidatus Liberibacter asiaticus', on huanglongbing-infected Citrus reticulata leaves of several maturity stages
Fig. 3. The major EPG variables of Diaphorina citri adults feeding on citrus leaves of several maturity stages. Mean (+SE) (A) durations of pathway phase (C), xylem phase (G) and phloem phase (E1+E2) (B) durations of phloem salivation (E1), phloem ingestion (E2) and salivation before phloem ingestion (E1 before E2) (C) percentage of salivation in total phloem activities (E1/E1+E2) (D) time from start to first salivation in phloem (Time to first E1) and to the first ingestion from phloem (Time to first E2) and (E) numbers of single E1 (single salivation) and E1 followed by E2 (salivation followed by ingestion). Within the same series, means capped by the same letter are not significantly different according to Duncan's Multiple Range test (P> 0.05).
Figure 3 in Severe glomerular disease in juvenile grey snapper Lutjanus griseus L. in the Gulf of Mexico caused by the myxozoan Sphaerospora motemarini n. sp.
Figure 3. SSU rDNA-based maximum likelihood (GTR + Γ model) tree of 26 myxosporean sequences showing the phylogenetic position of Sphaerospora motemarini n. sp. amongst all other polysporoplasmid Sphaerospora spp. sequenced to date (red) and within the Sphaerospora sensu stricto clade (yellow). Members of marine (blue) and freshwater (green) myxosporean lineages were used as outgroups. Maximum likelihood bootstraps/maximum parsimony bootstraps/Bayesian posterior probabilities shown at nodes. Dashes indicate bootstrap values <50 or not present in the maximum parsimony or Bayesian tree.
Figure 2 in Severe glomerular disease in juvenile grey snapper Lutjanus griseus L. in the Gulf of Mexico caused by the myxozoan Sphaerospora motemarini n. sp.
Figure 2. Line drawing of spore of Sphaerospora motemarini n. sp. summarizing all morphological details in two dimensions; spore with bilateral symmetry, labels given only on one side: SV = spore valve, VN = nucleus of valve cell, OP = ornamental surface pits on posterior part of spore valve, PC = polar capsule containing coiled polar filament (PF), PN = nucleus of polar capsule, SP = uninucleated sporoplasms (6); bar = 5 µm.
Figure 1 in Severe glomerular disease in juvenile grey snapper Lutjanus griseus L. in the Gulf of Mexico caused by the myxozoan Sphaerospora motemarini n. sp.
Figure 1. Morphology and histopathology of Sphaerospora motemarini n. sp. in grey snapper, Lutjanus griseus. (A) Mature spore in fresh kidney smear showing thickened suture at apical part (transparent arrowhead), two prominent bulges at posterior part (black arrowheads) and valve surface ornamentation (detailed in D) at the posteriolateral part of the spore; bar = 10 µm. (B) DAPI nuclear staining showing polysporoplasmic nature of spore (4 out of 6 sporoplasms visible in plane of image); bar = 10 µm. (C) Pseudoplasmodium containing two croissant-shaped sporoplasms (only visible around left spore) and two spores; bar = 10 µm. (D) SEM showing spore surface ornamentation in the shape of pits providing an opening to a multilayered canal system; bar = 5 µm. (E) Fresh smear of kidney showing early plasmodial stages (arrowheads) in a glomerulus; bar = 20 µm. (F–H) Histological sections stained with H&E; bar = 50 µm (F). Histopathological changes showing massive enlargement of renal corpuscles, with arrows in small insert (bottom left) indicating uninfected corpuscles of normal size in an uninfected kidney; bar = 50 µm. (G) Thickening of Bowman's capsule (arrows) and proliferation of mesangial cells; bar = 50 µm. (H) Engulfment of a spore by a melanin-rich macrophage (brown color); bar = 10 µm.
Fig. 1 in Apparent effect of chronic Plasmodium infections on disease severity caused by experimental infections with Mycoplasma gallisepticum in house finches
Fig. 1. Mean severity of eye lesions ± SE (circles), and M. gallisepticum-load (log (qPCR+1)) (triangles) of birds infected through horizontal transmission with the CA2015 strain of M. gallisepticum. Birds in which Plasmodium was detected by PCR (grey symbols) developed more severe disease than birds in which Plasmodium was not found (white symbol). As there is no significant interaction between M. gallisepticum ‾strain and Plasmodium infection (Table 2) the results for the other M. gallisepticum strains are qualitatively similar and therefore not shown.
The impact of severity of acute respiratory distress syndrome following cardiac arrest on neurologic outcomes
<p>Overall survival rates at 28 days in patients with and without ARDS. ARDS = acute respiratory distress syndrome</p>
Figure 6 in Genetic divergences of South and Southeast Asian frogs: a case study of several taxa based on 16S ribosomal RNA gene data with notes on the generic name Fejervarya
Figure 6. Maximum likelihood (ML) tree of bufonid frogs based on nucleotide sequences of the mitochondrial 16S rRNA gene with Leptophryne borbonica as an outgroup. The bootstrap support (>50%) is indicated at nodes in the order of ML (500) replicates. Asterisks represent Bayesian posterior probability (BPP; * ≥95%). Specimens examined in this study are indicated by boldface type.
Figure 2 in Genetic divergences of South and Southeast Asian frogs: a case study of several taxa based on 16S ribosomal RNA gene data with notes on the generic name Fejervarya
Figure 2. Maximum likelihood (ML) tree based on nucleotide sequences of the mitochondrial 16S rRNA gene from 88 haplotypes of frogs (Table 1), with Xenopus laevis as an outgroup. Bootstrap support (>50%) is indicated at nodes in the order of ML (1000) replicates. Asterisks represent Bayesian posterior probability (BPP; * ≥95%).
Text-fig. 3. Coeloma vigil A. MILNE-EDWARDS. Nearly complete specimens from several different layers. A – layer 15; B – layer 11; C – layer 16. All specimens are deposited at KGP MH. Key: ch=chelipeds; es=eye stalks; p=pereiopods. Scale bar 10 mm. Specimens were covered with ammonium chloride prior to photography. in The Priabonian Bryozoan-Decapod Association From The Borové Formation (The Ďurkovec Quarry, Ne Slovakia) And Its Palaeoecological Implications
Text-fig. 3. Coeloma vigil A. MILNE-EDWARDS. Nearly complete specimens from several different layers. A – layer 15; B – layer 11; C – layer 16. All specimens are deposited at KGP MH. Key: ch=chelipeds; es=eye stalks; p=pereiopods. Scale bar 10 mm. Specimens were covered with ammonium chloride prior to photography.
Figure 1 in Little Fire Ant, Wasmannia auropunctata (Roger) (Hymenoptera: Formicidae), Established at Several Locations on Guam
Figure 1. Map collection sites (after Burdick 2006) of W. auropunctata on Guam: (a) Primo Northern Wasteland, Yigo (N 13.5411, E 13.5411); (b) Nimitz Hill, Piti (N 13.4612, E 144.7080); (c) Pigua, Merizo (N 13.2648, E 144.6719);(d) Santa Rita (N 13.3919, E 144.6671); (e) Going to Veteran's Park, Umatac (N 13.3037, E 144.6742); (f) Matgue River, Piti (N 13.4685, E 144.7078); (g) Nimitz Hill, Piti (N 13.4641, E 144.7039).
Fig. 1 in Severe coenurosis caused by larvae of Taenia serialis in an olive baboon (Papio anubis) in Benin
Fig. 1. Clinical presentation of the baboon with the clear presence of swellings in various areas of the body: ventral abdominal and thoracic parts, inner part of forearms, intermandibular region (arrow heads) and dorsal region also.
Figure 5 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 5. BEAST chronogram of divergence of the representatives of the genus Cricotopus. Specimens collected and sequenced in this study are demonstrated in bold. Time to most recent common ancestor (tmrca) was estimated for the lettered nodes (in red) which correspond with those in Table 4. The time scale is in millions of years before present.
Figure 4. A neighbour-net phylogenetic network constructed using 106 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 4. A neighbour-net phylogenetic network constructed using 106 COI sequences of the genus Cricotopus and two COI sequences Orthocladius sp. (outgroup). For the clarity of the network, bootstrap support values of the nodes are not demonstrated.
Figure 3 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 3. Bayesian tree based on the analysis of COI sequences. Node-associated values (in red) correspond to ML bootstrap support (BS) and BI posterior probabilities (PP), respectively. Full support (100%/1.00) is marked with a bold circle.
Figure 2 in Evolutionary relationships among several species from the genus Cricotopus (Diptera: Chironomidae): What about Turkish representatives of this genus?
Figure 2. Saturation plot for transitions (blue crosses) and transversions (green triangles). The x axis shows the genetic distance based on the GTR model, while the y axis shows the proportion of transitions and transversions. The lines show the trends of the variance of transitions and transversions with increasing genetic distance.
Fig. 3 in Toxicity for control of Frankliniella schultzei and Selenothrips rubrocinctus (Thysanoptera: Thripidae) of several common synthetic insecticides
Fig. 3. The bioassays to evaluate the toxicity of selected insecticides on common blossom thrips, Frankliniella schultzei, and red-banded thrips, Selenothrips rubrocinctus, were conducted in 90 mL plastic cups. Each cup had 10 thrips and a 3 cm long piece of insecticide-treated bean.
Fig. 1 in Toxicity for control of Frankliniella schultzei and Selenothrips rubrocinctus (Thysanoptera: Thripidae) of several common synthetic insecticides
Fig. 1. Adult Frankliniella schultzei. Photograph by Ittipon Bannakan, Insect Taxonomy Group, the Entomology and Zoology Division, Plant Protection Research and Development office, Department of Agriculture, Bangkok, Thailand.
Fig. 2. Several G. truncatula within a in A proposed ectochory of Galba truncatula snails between wallow sites enhances transmission of Fascioloides magna at gemenc, in Hungary
Fig. 2. Several G. truncatula within a shrinking puddle. The amphibious snails are distributed more or less evenly on the wettest parts of mud but not in the water. A footprint of red deer is on the left. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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.