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Figure 1. a–f in Parasitoids reared from galls of Stefaniola sp. (Diptera, Cecidomyiidae) on Haloxylon spp. in China, with redescription of Mesopolobus quadrimaculatus Dzhanokmen (Chalcidoidea, Pteromalidae)
Figure 1. a–f: Mesopolobus quadrimaculatus Dzhanokmen: a–e (♀), f (♂). a: Body, dorsal view; b: head, frontal view; c: head and mesosoma, dorsal view; d: scutellum and propodeum, dorsal view; e: fore wing; f: head, frontal view, and antennae.
Fig. 2 in Analyzing the mass-rearing system of the California red scale parasitoid Aphytis melinus (Hymenoptera: Aphelinidae)
Fig. 2. Production of Aphytis melinus over the period in which the pilot system was working, from 18 March 2010 to 20 Jun 2011: (a) Total production per day, when different cages were in production at the same time and collection was every 2 to 3 days; (b) Total production per cage. Each bar in (b) represents the production of an individual cage, and is displayed as the date when parasitoid emergence began.
Fig. 1 in Analyzing the mass-rearing system of the California red scale parasitoid Aphytis melinus (Hymenoptera: Aphelinidae)
Fig. 1. Parasitoid (Aphytis melinus) production (as percentage of the total production given as mean ± SE) in the production cages: (a) daily emergence; (b) cumulative emergence.
Fig. 1 in The effects of laboratory rearing diet on recruitment behavior of Wasmannia auropunctata (Hymenoptera: Formicidaea)
Fig. 1. Mean ± SE difference in recruitment rates of laboratory raised Wasmannia auropunctata to non-toxic baits: Hawaii Ant Lab gel bait, 50% gelled sucrose solution, and tuna between pre- and post-treatment measurements of the multi-choice laboratory experiment (n = 5 colonies). Bars in each group with different letters above have statistically different means (P <0.05). Colonies were exposed to their respective dietary treatment (buffet plus crickets: n=5, vegetable oil wick plus crickets: n=5, 25% sucrose solution plus crickets: n=5, and pureed tuna plus crickets: n=5) for 49 d. Means represented in this chart are based on raw data for visualization and are not the reported marginal means.
Fig. 2 in The effects of laboratory rearing diet on recruitment behavior of Wasmannia auropunctata (Hymenoptera: Formicidaea)
Fig. 2. Recruitment rates (mean number of ants ± SE) of wild Wasmannia auropunctata to the Hawaii Ant Lab gel bait, 50% gelled sucrose solution, and tuna for multi-choice (n = 6 per treatment) and no-choice (n = 6 per treatment) field experiments. Bars within clusters with different letters above have statistically different means (P <0.05). Means represented in this chart are based on raw data for visualization and not proportional results from the Poisson distributed generalized linear mixed model as reported.
Fig. 2 in Laboratory rearing of Bagrada hilaris (Hemiptera: Pentatomidae) under quarantine conditions in Florida, USA
Fig. 2. Mean number of eggs oviposited by 10 Bagrada hilaris females on dental wicks, cotton balls, or Kimwipes in no-choice and choice tests. There was a significant effect of substrate type on the number of eggs oviposited in both the no-choice (F = 7.981; df = 2; P <0.001) and choice (F = 28.61; df = 2; P <0.001) tests.
Fig. 1 in Laboratory rearing of Bagrada hilaris (Hemiptera: Pentatomidae) under quarantine conditions in Florida, USA
Fig. 1. Large cages for no-choice and choice tests for evaluating the preference of Bagrada hilaris for 3 artificial oviposition substrates: dental wicks, cotton balls, or Kimwipes.
Fig. 4 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)
Fig. 4. Monthly water temperatures (circles) and pH (triangles) recorded from the shoreline of Lake Oku between 2008/2009 and 2013. Error bars represent SEM.
Fig. 1 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)
Fig. 1. Male (top) and female (bottom) adults of Xenopus longipes in the collection at ZSL London Zoo (ZIMS ID 7441).
Fig. 3. Aquarium for X. longipes, set within a in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)
Fig. 3. Aquarium for X. longipes, set within a custom built, centrally filtered system (inset photograph) at ZSL London Zoo. Life support system and sump not shown – see text for details.
Fig. 2 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)
Fig. 2. Keratinized nuptial pads on the inside surfaces of the front limbs of male (A and C) and cloaca of a female X. longipes (B); note the cloacal papillae, which are absent in male frogs.
Fig. 5 in Breeding and rearing the Critically Endangered Lake Oku Clawed Frog (Xenopus longipes Loumont and Kobel 1991)
Fig. 5. Gosner stage progression of the most rapidly developing X. longipes tadpole. Hatching to metamorphosis took 193 days, but smaller tadpoles had only reached stage 35 by this point.
Fig. 5 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 5. Micrograph of the brain on infected jaguar. Schizonts inside macrophages contain numerous round to oval 1–2 μm diameter basophilic organisms (merozoites). HE.
Fig. 4 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 4. Micrograph of the pancreas on infected jaguar. The macrophages are enlarged up to twice normal size and contained cytoplasmic schizonts. Note eccentric and pyknotic nuclei of macrophages. HE.
Fig. 3 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 3. Micrograph of the pancreas on infected jaguar. The central blood vessel is partially obstructed by macrophages containing high numbers of C. felis schizonts. HE.
Fig. 2 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 2. Gross findings of Cytauxzoon felis fatal infection in a jaguar. The spleen is severely enlarged.
Fig. 1 in Fatal infection caused by Cytauxzoon felis in a captive-reared jaguar (Panthera onca)
Fig. 1. Gross findings of Cytauxzoon felis fatal infection in a jaguar. Moderate icterus in the ocular mucosa. The enophthalmos indicates severe dehydration.
Fig. 2 in A sustainable mass rearing method for western flower thrips, Frankliniella occidentalis (Thysanoptera: Thripidae)
Fig. 2. Diagram of life cycle, rearing procedures, and label coding for Frankliniella occidentalis. (A) Frankliniella occidentalis male (lef) and female (right) adults; (B) egg-infested cotyledon; (C) nymph-infested cotyledon; (D) pupae under filter paper in rearing container; cots = cotyledons.
Fig. 1 in A sustainable mass rearing method for western flower thrips, Frankliniella occidentalis (Thysanoptera: Thripidae)
Fig. 1. (A) Shirofumi soybean sprout with cotyledons ready to harvest (circled). (B) Metal tray housing immature stages of Frankliniella occidentalis in insect rearing containers with secondary standard Petri dish lids on top of ventilated mesh lids. Records of dates maintained and life stages present in containers are kept on each colony lid.
Fig. 2 in Applications of molecular diagnostics for quality control in rearing of Spodoptera frugiperda (Lepidoptera: Noctuidae) larvae for experimental use
Fig. 2. Relative abundance of diversity of viruses found in the metagenomic analysis of dead and healthy larvae of Spodoptera frugiperda.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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