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Fig. 2. Type II in Effect of temperature on functional response of Aphidius gifuensis (Hymenoptera: Braconidae) parasitizing Myzus persicae (Hemiptera: Aphididae)
Fig. 2. Type II functional response curves fitted by Roger's random parasitoid equation (RRPE) of Aphidius gifuensis against Myzus persicae at various temperatures.
Fig. 1. Type II in Effect of temperature on functional response of Aphidius gifuensis (Hymenoptera: Braconidae) parasitizing Myzus persicae (Hemiptera: Aphididae)
Fig. 1. Type II functional response curves fitted by Holling's disc equation (HDE) of Aphidius gifuensis against Myzus persicae at various temperatures.
Fig. 1 in Biology of Telenomus pachycoris (Hymenoptera: Scelionidae), a parasitoid of eggs of Pachycoris torridus (Hemiptera: Scutelleridae): the effects of egg age, exposure time, and temperature
Fig. 1. Number of generations of Telenomus pachycoris reared in Pachycoris torridus eggs at different constant temperatures with 70 ± 10% RH and a photoperiod of 12:12 h L:D.
Fig. 1 in First report of economic injury to tomato due to Zeugodacus tau (Diptera: Tephritidae): relative abundance and effects of cultivar and season on injury
Fig. 1. Seasonal pattern of Zeugodacus tau male adults (mean ± SE) captured by Cue-lure-based traps in tomato in (a) season 1, and (b) season 2.
Fig. 1 in Timing of irradiation and male mating history effects on female remating in Anastrepha ludens (Diptera: Tephritidae)
Fig. 1. Interaction between age of pupal irradiation (24, 48, or 72 h before emergence) and male previous sexual experience (virgin, once mated, or twice mated) of the GSS strain of A. ludens (Tapachula-7) males on wild female likelihood to remate (N = 945).
Fig. 1 in Effect of temperature on the population growth of Tirathaba rufivena (Lepidoptera: Pyralidae) on Areca catechu (Arecaceae)
Fig. 1. Survival rates for immature stages and the entire development period (egg to adult) of Tirathaba rufivena at 5 constant temperatures. Each value represents the mean of 3 replicates for each temperature, and bars indicate the standard error.
Fig. 2 in Effect of temperature on the population growth of Tirathaba rufivena (Lepidoptera: Pyralidae) on Areca catechu (Arecaceae)
Fig. 2. Mean numbers of eggs deposited per Tirathaba rufivena female at 5 constant temperatures. Each value represents the mean of 3 replicates for each temperature, and bars indicate the standard error.
Fig. 2 in What drives population-level effects of parasites? Meta-analysis meets life-history
Fig. 2. Funnel plot of effect size (Hedges' g) by standard error (SE). The white circles represent studies included in the meta-analysis. The black circles represent missing imputed studies. The white diamond represents overall effect size as calculated in the meta-analysis, and the black diamond represents the corrected effect size.
Fig. 1 in What drives population-level effects of parasites? Meta-analysis meets life-history
Fig. 1. Forest plot of effect sizes (rectangles) and confidence intervals (bars) for each study and the effect averaged across all studies (diamond).
Fig. 3. A in What drives population-level effects of parasites? Meta-analysis meets life-history
Fig. 3. A meta-regression (random effects model) of effect size against host average lifespan using the complete dataset (n = 60). The slope of this regression is significant (p = 0.05).
Fig. 1 in Co-invaders: The effects of alien parasites on native hosts
Fig. 1. Schematic diagram of processes involved in species invasions and coinvasions. (a) Free-living aliens. The light blue oval shape represents a new area, outside the natural range of the alien species, shown in red. Arrows indicate movement of alien species through the phases of introduction, establishment and invasion of the habitat of the native species, shown in blue. Vertical bars represent barriers to be overcome in each phase. (b) Parasitic aliens. The alien host species (in red) contains an alien parasite species. The alien parasite goes through the processes of introduction, establishment and spread with its original host and then switches to a native host species (in blue) to become a co-invader. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 2 in Co-invaders: The effects of alien parasites on native hosts
Fig. 2. (a) Relative proportions of taxa represented in 98 examples of co-introduced parasites: prokaryotes (viruses and bacteria); protozoans; helminths (platyhelminths, nematodes and acanthocephalans); arthropods (crustaceans, arachnids); and a miscellaneous group including fungi, myxozoans, annelids, molluscs and pentasomids. (b) Relative proportions of alien hosts represented in 98 examples of cointroductions: molluscs; arthropods; fishes; mammals; and other vertebrates (amphibians, reptiles and birds). (c) Number of co-introduced parasite species with direct and indirect life cycles which have switched (black bars) or not switched (white bars) from alien to native host species.
Fig. 6 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 6. SSU rDNA maximum likelihood phylogenetic tree of 16 Kudoa spp. Kudoa islandica is robustly and consistently placed with other Kudoa taxa in all analyses, but is not well supported in the clade it is placed in. Numbers at the nodes represent bootstrap support from 1000 samplings, nodes with a support of <50 are considered not supported (ns).
Fig. 4 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 4. Line drawings of Kudoa islandica n. sp. in apical view (A) and lateral view (B). Scanning electron microscope images of K. islandica n. sp. (C–E). Mature spore in lateral view showing extruded polar filaments (arrow) (C). Single spore in apical view (D) showing the sutures of the four valves (broad arrows), the four apical projections (thin arrow) and cytoplasmic projections (arrowhead). Single spore in posterior view (E) showing the suture of the four valves (broad arrows), Scale bars: (A) and (B) = 2 µm; (C), (D) and (E) = 1 µm.
Fig. 3 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 3. Fresh mature spores of Kudoa islandica n. sp. as seen in fresh squash preparations from muscular tissue of Atlantic wolffish, Anarhichas lupus. Note the protruding polar filament of one of the spores (arrow). Nomarski differential interference contrast. Scale bar = 10 µm.
Fig. 5 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 5. (A) and (B) Muscle section from lumpfish, Cyclopterus lumpus, fixed 24 h post mortem. (A) Ruptured Kudoa plasmodia with subsequent liberation of mature spores causing focal necrosis of the muscle fibre enveloping the plasmodium. (B) Higher magnification showing liberated spores (arrows) and a focal necrosis in the vicinity of the spores (asterisk). (C) Muscle section of an uninfected fish at approx. 48 h p.m. (D) Section of muscle of a heavily infected fish at approximately 48 h p.m. showing extensive myoliquefaction (asterisk). (E) A close up of the affected area showing numerous Kudoa spores (arrowhead) and the associated liquefactive necrosis. Scale bars: (A) = 50 µm, (B) = 10 µm, (C) and (D) = 200 µm, (E) = 10 µm. Abbreviations: MF = Muscle fibres, AC = Adipocytes.
Fig. 2 in Negative effects of Kudoa islandica n. sp. (Myxosporea: Kudoidae) on aquaculture and wild fisheries in Iceland
Fig. 2. (A) Stained histological section of a lumpfish muscle showing a considerable portion of the muscle fibres substituted with Kudoa islandica n. sp. plasmodia. (B) A single infection. (C) A double infection. (D) Multiple infection; numerous plasmodia developing inside a single muscle fibre, separated from each other and the muscle tissue with a thin membrane (arrows). (E) Plasmodial membranes separating two plasmodia (arrows). Inside each plasmodium are numerous mature Kudoa spores. Scale bars: (A) = 300 µm (B) and (C) = 25 µm; (D) = 150 µm; (E) = 5 µm.
Fig. 1 in Effect of pH on the Early Development of the Biofouling Ascidian .
Fig. 1. Average number of individual Ciona robusta found in 2 mL subsample within each replicate flask (a) varied across pH and time (3–58 hpf). To enable comparison between treatments that had different initial concentration, larval count was normalized against the average of the triplicate flask of the given pH at 3 hpf. In other words, the average between the three replicates at 3 hpf for a given pH = 1. This survivorship estimate (b), indicated by the relative density across four pHs (pH 8.0, pH 7.6, pH 7.2, and pH 6.8) from fertilization to meta-metamorphosis (adhesion period at 21 hpf), did not vary with time or pH (ANCOVA, Table 2). Each dot represents a single replicate flask. The dotted regression lines were not significant but illustrate the general trends (Table 3).
Fig. 3 in Effect of pH on the Early Development of the Biofouling Ascidian .
Fig. 3. The breakpoint pH, represented by the dotted line, varied throughout ontogeny. The breakpoint was identified by piecewise regression. Only five representative time points were presented (see Table 4 for the full regression statistics for all stages). The scale bars of the insets were 100 µm.
Fig. 2 in Effect of pH on the Early Development of the Biofouling Ascidian .
Fig. 2. Ocean acidification led to developmental delay in Ciona robusta. The mean and standard error for the proportion of embryo/larvae at a given stage relative to the total larval count at a particular time point were plotted. Note that 100% represents a different relative larval density for each bar (see Figure 1 for larval density).
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.