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Figure 4 in Impact of a large dam on reproduction of a non-migratory teleost species, Acestrorhynchus lacustris (Characiformes: Acestrorhynchidae)
Figure 4. Testis in different maturation stages and respective transversal sections stained by HE. (A) early maturation, (B) advanced maturation/mature, (C) partially spent; Z= spermatozoa; C2= secondary spermatocytes T= spermatids; ST= seminiferous tubules. Scale bars represent A= 100 µm, B= 200 µm and C= 500 µm.
Figure 3 in Impact of a large dam on reproduction of a non-migratory teleost species, Acestrorhynchus lacustris (Characiformes: Acestrorhynchidae)
Figure 3. Ovaries in different maturation stages and the respective transversal sections stained by HE.(A) resting, (B) initial maturation, (C) advanced maturation/mature, (D) partially spawned, (E) totally spawned ovaries, (F) post-ovulatory follicle, (G) yellow body. O1= early perinucleolar follicles; O2= late perinucleolar follicles; O3= pre-vitellogenic follicles; O4= vitellogenic follicles; POF= post-ovulatory follicle; YB= yellow body. Scales bars represent 100 µm.
Figure 2 in Impact of a large dam on reproduction of a non-migratory teleost species, Acestrorhynchus lacustris (Characiformes: Acestrorhynchidae)
Figure 2. Frequency (%) and size classes of vitelogenic follicles (µm) of A. lacustris from fully grown ovaries of A. lacustris. Different bar colours indicate statistically significant differences between the diameter classes (p<0.05).
Figure 1 in Impact of a large dam on reproduction of a non-migratory teleost species, Acestrorhynchus lacustris (Characiformes: Acestrorhynchidae)
Figure 1. Sampling sections of the São Francisco River, downstream from Três Marias Dam. Section 1: immediately downstream the Dam; Section 2: immediately after the confluence with Abaeté River. UTM coordinates.
Figure 2 in Reproductive diseases in captive Agoutis (Dasyprocta leporina)
Figure 2. Necropsy of Adult Agouti with offspring in the right uterine horn and enlarged bladder (Source: Jones et al.,2020).
Fig. 7 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 7. The correlation between the concentration of 20-hydroxyecdysone used for treatment and the mean number of eggs deposited on the treated seedlings. R represents the correlation coefficient; the symbol ** next to the coefficient indicates that the correlation between X and Y was significant at P <0.01.
Fig. 6 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 6. The morphological changes in diamondback moth larvae and a pupae caused by ingestion of exogenous dietary 20-hydroxyecdysone. a, Exosmosis of ecdysial fluid and an additional molt (15 ×); b, failure to shed the head capsule (30 ×); c, failure to shed the exuvium (20×); d, bulging of the hindgut (10 ×); and e, deformed pupa (10 ×).
Fig. 4 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 4. The correlation between the concentration of 20-hydroxyecdysone in diet and mean weight gain in 4th instars of diamondback moth. W0–24 h, W0–48 h, and W24–48 h represent mean weight gain at 24 h, at 48 h, and from 24 h to 48 h afer treatment, respectively. R represents the coefficient; the symbols * and ** next to the coefficient indicate that the correlation between X and Y was significant at P <0.05 and P <0.01, respectively.
Fig. 5 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 5. The correlation between the concentration of 20-hydroxyecdysone in diet and mean weight of diamondback moth pupae. P1, P2, P3, and P4 represent mean weight of pupae developed from the treated 1st, 2nd, 3rd, and 4th instars, respectively. R represents the coefficient; the symbol ** next to the coefficient indicates that the correlation between X and Y was significant at P <0.01.
Fig. 1 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 1. The arrangement of 20-hydroxyecdysone-treated radish seedlings in a cage. Digit 0 represents the control; digits 1–4 represent the radish seedlings treated with 0.050, 0.100, 0.200, and 0.400 mg/mL of 20E solutions in water, respectively.
Fig. 2 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 2. The correlation between the concentration of 20-hydroxyecdysone in diet and mean food consumption by diamondback moth larvae for each instar. C1, C2, C3, and C4 represent mean food consumption of 1st, 2nd, 3rd, and 4th instars, respectively. R represents the coefficient; the symbols * and ** next to the coefficient indicate that the correlation between X and Y was significant at P <0.05 and P <0.01, respectively.
Fig. 3 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 3. The correlation between the concentration of 20-hydroxyecdysone in diet and mean duration of each instar of diamondback moth larvae. D1, D2, D3, and D4 represent mean duration of 1st, 2nd, 3rd, and 4th instars, respectively. R represents the coefficient; the symbol ** next to the coefficient indicates that the correlation between X and Y was significant at P <0.01.
Fig. 8 in The effects of exogenous 20-hydroxyecdysone on the feeding, development, and reproduction of Plutella xylostella (Lepidoptera: Plutellidae)
Fig. 8. The longevity of adults fed on diet with exogenous dietary 20-hydroxy- ecdysone. The different lowercase letters above bars indicate statistically significant differences between mean longevity of adults fed on diet with different concentrations of 20-hydroxyecdysone (Tukey test, α = 0.05).
Fig. 1B in Reproduction of Tetrastichus howardi (Hymenoptera: Eulophidae) in Diatraea saccharalis (Lepidoptera: Crambidae) pupae at different temperatures
Fig. 1B). The maximum longevity of T. howardi was 50 d at 16 °C and the minimum was 2 d at 31 °C. The longevity of this parasitoid was 21 d at 25 °C. Tetrastichus howardi females began to oviposit on the same day they had contact with the host pupae. Parasitoid progeny production was greater when parasitism occurred during the 1st day of exposure to host pupae at all temperatures. About 90% of the offspring was pro-
Fig. 1 in Development and reproduction of Mallada basalis (Neuroptera: Chrysopidae) on artificial diets
Fig. 1. Developmental parameters of Mallada basalis fed during the immature stages of the F1 generation on the 3 artificial diets at 26 ± 1 °C. F1 egg hatch and pupation rates differed significantly among the 3 diet treatments and both parameters were significantly the greatest in the AD1 treatment and unacceptably small in the AD2 treatment. F1 adult emergence rates among the 3 diets did not differ significantly (P> 0.05). The F1 generation produced no eggs in the AD2 treatment. The hatch rate from F2 eggs in the AD1 treatment was significantly greater than in the AD3 treatment.
Fig. 1 - A in Short Communications First record of the presence and reproduction of the two-tailed pasha Charaxes jasius (Linnaeus 1767) (Lepidoptera: Nymphalidae) in northeastern Italy
Fig. 1 - A male observed in the xerothermic oasis of Monte Ceva on 7 September 2021. / Un maschio osservato nell'oasi xerotermica del Monte Ceva il 7 Settembre 2021.
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. 1. Teratocephalus lirellus Andrassy, 1969: A — трофико-сенсорный отΑеΛ теΛа; B — поΛовая система; C — фрагмент теΛа с боковым поΛем; D — хвост; E — фрагмент поΛовой системы и среΑней кишки; F, G — переΑний конец теΛа. am — амфиΑы, lf — боковое поΛе, v — вуΛьва, cc — гоΛовная капсуΛа, pu — заΑняя матка, au — переΑняя матка, r — ренетта, ep — экскреторная пора, o — яичник Fig. 1. Teratocephalus lirellus Andrassy, 1969: A — trophic-sensory part of the body; B — reproductive system; C — fragment of the body with a lateral field; D — tail; E — fragment reproductive system and intestine; F, H — anterior end of the body. am — amphid; lf — lateral field; v — vulva; cc — cephalic capsule; pu — posterior uterus; au — anterior uterus; r — renetta; ep — excretory pore; o — ovary in Recent data on soil nematodes of the families Teratocephalidae and Metateratocephalidae from Primorsky Region, Russia
Рис. 1. Teratocephalus lirellus Andrassy, 1969: A — трофико-сенсорный отΑеΛ теΛа; B — поΛовая система; C — фрагмент теΛа с боковым поΛем; D — хвост; E — фрагмент поΛовой системы и среΑней кишки; F, G — переΑний конец теΛа. am — амфиΑы, lf — боковое поΛе, v — вуΛьва, cc — гоΛовная капсуΛа, pu — заΑняя матка, au — переΑняя матка, r — ренетта, ep — экскреторная пора, o — яичник Fig. 1. Teratocephalus lirellus Andrassy, 1969: A — trophic-sensory part of the body; B — reproductive system; C — fragment of the body with a lateral field; D — tail; E — fragment reproductive system and intestine; F, H — anterior end of the body. am — amphid; lf — lateral field; v — vulva; cc — cephalic capsule; pu — posterior uterus; au — anterior uterus; r — renetta; ep — excretory pore; o — ovary
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
Fig. 4. Survival curves with 95 in Effect of temperature on growth, reproductive activity, and survival of the invasive bromeliad-eating weevil Metamasius callizona (Coleoptera: Curculionidae)
Fig. 4. Survival curves with 95% confidence intervals for Metamasius callizona adults at 3 temperatures. Numbers of individuals at time zero were: 16 °C, n = 54; 25 °C, n = 47; and 35 °C, n = 74.
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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.