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Figure 1 in Egg production and life history of Alona guttata Sars, 1862 (Cladocera, Chydoridae): implications for colonization of temporary ponds
Figure 1. Reproduction aspects and life cycle parameters of Alona guttata for 18 individuals grown under laboratory conditions. (Fed with R. subcapitata, controlled temperature of 22 ± 2 °C and photoperiod of 16 h light/8 h dark.)
Fig. 2 in Egg parasitoids of stink bugs (Hemiptera: Coreidae and Pentatomidae) on soybean and cowpea in Brazil
Fig. 2. Map of the known occurrence of the stink bug parasitoids Trissolcus basalis, Tr. urichi, Tr. teretis, Tr. bodkini, Telenomus podisi, Phanuropsis semiflaviventris, Neorileya flavipes, Ooencyrtus anasae, and Anastatus sp. in Brazil.
Fig. 1 in Egg parasitoids of stink bugs (Hemiptera: Coreidae and Pentatomidae) on soybean and cowpea in Brazil
Fig. 1. Female, lateral view. (1) Trissolcus urichi, (2) Trissolcus teretis, (3) Telenomus podisi, (4) Trissolcus bodkini, (5) Phanuropsis semiflaviventris, (6) Neorileya flavipes, (7) Anastatus sp., (8) Ooencyrtus anasae.
Fig. 1 in Comparison of the eggs size between two subspecies of the Kotschy's Gecko Mediodactylus kotschyi (Steindachner, 1870) (Reptilia: Gekkonidae) in Bulgaria
Fig. 1. Cluster analysis of the egg volume sizes of three subspecies of M. kotschyi from the current study and comparison with literary data.
Рис. 3. Teratocephalon hexahamus gen. n., sp. n.: A — трофико-сенсорный отΑеΛ теΛа; B — трофико-генитаΛьный отΑеΛ теΛа; C, D — переΑний конец теΛа. a — анус, am — амфиΑы, v — вуΛьва, cc — гоΛовная капсуΛа, ve — «жеΛуΑочек», pu — заΑняя матка, nr — нервное коΛьцо, rc — прямая кишка, au — переΑняя матка, r — ренетта, ep — экскреторная пора, o — яичник, e — яйцо Fig. 3. Teratocephalon hexahamus gen. n., sp. n.: A — trophic-sensory part of the body; B — trophic-reproductive part of the body; C, D — anterior end of the body. a — anus; am — amphids; v — vulva; cc — cephalic capsule; ve — "ventricle"; pu — posterior uterus; nr — nerve ring; pu — anterior uterus; r — renetta; rc — rectum; ep — excretory pore; o — ovary; e — egg in Recent data on soil nematodes of the families Teratocephalidae and Metateratocephalidae from Primorsky Region, Russia
Рис. 3. Teratocephalon hexahamus gen. n., sp. n.: A — трофико-сенсорный отΑеΛ теΛа; B — трофико-генитаΛьный отΑеΛ теΛа; C, D — переΑний конец теΛа. a — анус, am — амфиΑы, v — вуΛьва, cc — гоΛовная капсуΛа, ve — «жеΛуΑочек», pu — заΑняя матка, nr — нервное коΛьцо, rc — прямая кишка, au — переΑняя матка, r — ренетта, ep — экскреторная пора, o — яичник, e — яйцо Fig. 3. Teratocephalon hexahamus gen. n., sp. n.: A — trophic-sensory part of the body; B — trophic-reproductive part of the body; C, D — anterior end of the body. a — anus; am — amphids; v — vulva; cc — cephalic capsule; ve — "ventricle"; pu — posterior uterus; nr — nerve ring; pu — anterior uterus; r — renetta; rc — rectum; ep — excretory pore; o — ovary; e — egg
Рис. 2. Euteratocephalus montanus sp. n.: A — трофико-сенсорый и трофико-генитаΛьный отΑеΛы теΛа; B — хвост; C — трофико-генитаΛьный отΑеΛ теΛа; D — фрагмент теΛа с боковым поΛем; E, F — переΑний конец теΛа. am — амфиΑы, lf — боковое поΛе, v — вуΛьва, va — вагина, g — гемизониΑ, cc — гоΛовная капсуΛа, ve — «жеΛуΑочек», pr — преректум,r — ренетта, f — фазмиΑа,ep — экскреторная пора, o — яичник, e — яйцо Fig. 2. Euteratocephalus montanus sp. n.: A — trophic-sensory and trophic-reproductive parts of the body; B — tail; C — trophic-reproductive part of the body; D — fragment of the body with a side field; E, F — anterior end of the body. am — amphid, lf — lateral field; v — vulva; va — vagina; g — gemizonid; cc — cephalic capsule; ve — "ventricle"; pr — prerectum; r — renetta; f — phasmids, ep — excretory pore; o — ovary; e — egg in Recent data on soil nematodes of the families Teratocephalidae and Metateratocephalidae from Primorsky Region, Russia
Рис. 2. Euteratocephalus montanus sp. n.: A — трофико-сенсорый и трофико-генитаΛьный отΑеΛы теΛа; B — хвост; C — трофико-генитаΛьный отΑеΛ теΛа; D — фрагмент теΛа с боковым поΛем; E, F — переΑний конец теΛа. am — амфиΑы, lf — боковое поΛе, v — вуΛьва, va — вагина, g — гемизониΑ, cc — гоΛовная капсуΛа, ve — «жеΛуΑочек», pr — преректум,r — ренетта, f — фазмиΑа,ep — экскреторная пора, o — яичник, e — яйцо Fig. 2. Euteratocephalus montanus sp. n.: A — trophic-sensory and trophic-reproductive parts of the body; B — tail; C — trophic-reproductive part of the body; D — fragment of the body with a side field; E, F — anterior end of the body. am — amphid, lf — lateral field; v — vulva; va — vagina; g — gemizonid; cc — cephalic capsule; ve — "ventricle"; pr — prerectum; r — renetta; f — phasmids, ep — excretory pore; o — ovary; e — egg
Рис. 2. Фотографии Geomonhystera longisoma sp. nov., гоΛотип самца (a, c, d, g, h) и паратип самки (b, e, f, i): a, b — общий виΑ; с — переΑний конец теΛа; d, e — гоΛова; f — теΛо в обΛасти вуΛьвы и ануса; g — теΛо в обΛасти кΛоаки; h, i — хвост. Обозначения: an — анус; c.g. — карΑиаΛьные жеΛезы; cl — кΛоака; eg — яйцо; f.a. — фовея амфиΑ; gub — руΛек; in — среΑняя кишка; ols — внешние губные щетинки; ph — фаринкс; spic — спикуΛа; t — хвост. Масштаб: a, b — 100 мкм; с, f, i — 50 мкм; h — 20 мкм; d, e, g — 10 мкм Fig. 2. Light micrographs of Geomonhystera longisoma sp. nov., male holotype (a, c, d, g, h) and female paratype (b, e, f, i): a, b — general view; с — anterior body end; d, e — head; f — vulva and anus region; g — cloaca region; h, i — tail. Abbreviations: an — anus; c.g. — cardial glands; cl — cloaca; eg — egg; f.a. — fovea of amphid; gub — gubernaculum, ols — outer labial setae; in — intestine; ph — pharynx; spic — spicula; t — tail. Scale bars: a, b — 100 µm; с, f, i — 50 µm; h — 20 µm; d, e, g — 10 µm in Geomonhystera longisoma sp. nov. and Mongolotheristus tsalolichini sp. nov. (Nematoda, Monhysterida) from Mekong River mouth, Vietnam
Рис. 2. Фотографии Geomonhystera longisoma sp. nov., гоΛотип самца (a, c, d, g, h) и паратип самки (b, e, f, i): a, b — общий виΑ; с — переΑний конец теΛа; d, e — гоΛова; f — теΛо в обΛасти вуΛьвы и ануса; g — теΛо в обΛасти кΛоаки; h, i — хвост. Обозначения: an — анус; c.g. — карΑиаΛьные жеΛезы; cl — кΛоака; eg — яйцо; f.a. — фовея амфиΑ; gub — руΛек; in — среΑняя кишка; ols — внешние губные щетинки; ph — фаринкс; spic — спикуΛа; t — хвост. Масштаб: a, b — 100 мкм; с, f, i — 50 мкм; h — 20 мкм; d, e, g — 10 мкм Fig. 2. Light micrographs of Geomonhystera longisoma sp. nov., male holotype (a, c, d, g, h) and female paratype (b, e, f, i): a, b — general view; с — anterior body end; d, e — head; f — vulva and anus region; g — cloaca region; h, i — tail. Abbreviations: an — anus; c.g. — cardial glands; cl — cloaca; eg — egg; f.a. — fovea of amphid; gub — gubernaculum, ols — outer labial setae; in — intestine; ph — pharynx; spic — spicula; t — tail. Scale bars: a, b — 100 µm; с, f, i — 50 µm; h — 20 µm; d, e, g — 10 µm
Fig. 3 in Effect of humidity on fecundity and egg incubation of Frankliniella bispinosa and Frankliniella occidentalis (Thysanoptera: Thripidae)
Fig. 3. Mean daily fecundity (± SE) of Frankliniella bispinosa and F. occidentalis for data pooled across time intervals in laboratory experiments at constant 23 °C and 4 relative humidity levels. Means with the same letter are not significantly different according to ANOVA and subsequent Tukey's HSD test (α = 0.05).
Fig. 2 in Effect of humidity on fecundity and egg incubation of Frankliniella bispinosa and Frankliniella occidentalis (Thysanoptera: Thripidae)
Fig. 2. Mean fecundity (± SE) per female of Frankliniella occidentalis at 12 h intervals in laboratory experiments at constant 23 °C and 4 relative humidity levels.
Fig. 1 in Effect of humidity on fecundity and egg incubation of Frankliniella bispinosa and Frankliniella occidentalis (Thysanoptera: Thripidae)
Fig. 1. Mean fecundity (± SE) per female of Frankliniella bispinosa at 12 h intervals in laboratory experiments at constant 23 °C and 4 relative humidity levels.
Fig. 4 in Effect of humidity on fecundity and egg incubation of Frankliniella bispinosa and Frankliniella occidentalis (Thysanoptera: Thripidae)
Fig. 4. Mean time of egg hatch (± SE) for Frankliniella bispinosa and F. occidentalis in laboratory experiments at constant 23 °C and 4 relative humidity levels. Means with the same letter are not significantly different according to ANOVA and subsequent Tukey's HSD test (α = 0.05).
Fig. 2 in Monitoring the establishment and flight phenology of parasitoids of emerald ash borer (Coleoptera: Buprestidae) in Michigan by using sentinel eggs and larvae
Fig. 2. Percentage of parasitism by Tetrastichus planipennisi of emerald ash borer larvae in larval sentinel logs (pooled by sample date, i.e., the date that larval sentinel logs were collected) in Nancy Moore and Burchfield Parks, Michigan, in (A) 2011, (C) 2012, and (E) 2013, and by Atanycolus spp. in (B) 2011, (D) 2012, and (F) 2013. The secondary Y-axis is growing degree day base 10 °C (GDD10) using the Baskerville–Emin method.
Fig. 1 in Monitoring the establishment and flight phenology of parasitoids of emerald ash borer (Coleoptera: Buprestidae) in Michigan by using sentinel eggs and larvae
Fig. 1. Percentage of parasitism by Oobius agrili of emerald ash borer eggs on all egg sentinel logs (pooled by sample date, i.e., the date that egg sentinel logs were collected) in Central Park, Michigan, in (A) 2011 and (C) 2012, and on individual egg sentinel logs pooled over all sample dates in (B) 2011 and (D) 2012. The secondary Y-axis is growing degree day base 10 °C (GDD10) using the Baskerville–Emin method.
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 Establishment in the field of Cleruchoides noackae (Hymenoptera: Mymaridae), an exotic egg parasitoid of Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae)
Fig. 1. Total number of Cleruchoides noackae (Hymenoptera: Mymaridae) adults emerged from Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae) eggs per d that were parasitized in the laboratory (23 ± 2 °C, 60 ± 10% RH, and 12:12 h L:D photoperiod) and from eggs of this pest collected in the field.
Fig. 3 in A standardised faecal collection protocol for intestinal helminth egg counts in Asian elephants, Elephas maximus
Fig. 3. Pairwise comparisons of faecal egg counts (in EPG) for samples taken from different faecal boluses produced in one defecation event of (a) first and middle boluses, (b) first and last boluses, (c) middle and last boluses, all with 95% confidence intervals. For each of (a‾c) 40 samples collected from 20 elephants. Data collected for one elephant not shown, with one extreme data point removed in each of a‾c, to allow for better presentation of plots.
Fig. 2 in A standardised faecal collection protocol for intestinal helminth egg counts in Asian elephants, Elephas maximus
Fig. 2. Regression of the faecal egg counts (in EPG) for samples taken of the centre and edge of a single faecal bolus with 95% confidence intervals, 474 samples collected from 119 elephants.
Fig. 1 in A standardised faecal collection protocol for intestinal helminth egg counts in Asian elephants, Elephas maximus
Fig. 1. Averaged helminth egg counts for every elephant host sampled for each experiment; investigating egg distribution within (a) an individual bolus (centre and edge samples), 474 samples from 119 elephants and (b) multiple boluses (centre and edge samples from different boluses), 120 samples from 20 elephants, (c) when determining optimal sampling time, 94 samples from 47 elephants, and (d) if storage methods had any impact on egg recovery during faecal egg counts (FEC), 132 samples from 33 elephants. Helminth eggs were always aggregated within host elephants, with few hosts having substantial parasite burdens (in excess of 200 EPG) and the majority having none or insubstantial levels of infection.
Fig. 4 in A standardised faecal collection protocol for intestinal helminth egg counts in Asian elephants, Elephas maximus
Fig. 4. Faecal egg counts (in EPG) were significantly decreased in samples which had been stored in 10% formalin or 10% formol saline in comparison to subsamples collected at the same time but analysed as fresh, without storage in fixative solution. This figure is based on 132 samples collected from 33 elephants, with data lying between the first and third quartiles as represented by the top and bottom horizontal lines of the boxplot. The data range is shown by the vertical black lines, with the median of each dataset represented by the middle horizontal line within each boxplot and with any outliers shown as points.
Fig. 3 in Peroral Echinococcus multilocularis egg inoculation in Myodes glareolus, Mesocricetus auratus and Mus musculus (CD-1 IGS and C57BL/6j)
Fig. 3. Number of metacestodes of varying sizes in individual species at 6 wpi (M. glareolus at 8 wpi) after receiving 100 viable E. multilocularis eggs. A <1 mm, B 1 - Ý2 mm, C> 2 - Ý3 mm, D> 3 - Ý4 mm, E 4 - Ý5 mm, F> 5 mm. Data from current study and (Woolsey et al., 2015a; Woolsey et al., 2015b).
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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.