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Figure 3 in The nest, eggs and nestling development of Fork-tailed Woodnymph Thalurania furcata boliviana
Figure 3. Mass gain of Fork-tailed Woodnymph Thalurania furcata boliviana nestlings in Acre, Brazil, over the development period (measurements taken every two days between 14 January and 1 February 2016).
Figure 7 in Sex ratio, oocyte development and spawning season of Mediterranean moray eel (Muraena helena) from the northern coast of Tunisia
Figure 7. – Section of gonad, illustrating the spawning capable reproductive phase of ovary (CA = cortical alveolar oocyte; Vtg3 = tertiary vitellogenic oocyte).
Figure 5 in Sex ratio, oocyte development and spawning season of Mediterranean moray eel (Muraena helena) from the northern coast of Tunisia
Figure 5. – Section of gonad, illustrating the immature phase of ovary (PG = primary growth oocyte; OW = ovarian wall).
Figure 2 in Sex ratio, oocyte development and spawning season of Mediterranean moray eel (Muraena helena) from the northern coast of Tunisia
Figure 2. Seasonal variation of the gonadosomatic index (GSI), hepatosomatic index (HSI) and relative condition factor (CF) of Muraena helena from the northern coast of Tunisia. Bars are mean values (± 2 standard errors).
Figure 2. Passion fruit species under different irrigation intervals. A. Passiflora gibertii with a 4 in Development and physiological aspects of three species of passion fruit submitted to water stress
Figure 2. Passion fruit species under different irrigation intervals. A. Passiflora gibertii with a 4-day interval; B. P. gibertii with a 8-day interval; C. P. gibertii with a 12-day interval; D. P. foetida with a 4-day interval; E. P. foetida with a 8-day interval; F. P. foetida with a 12-day interval; G. P. edulis with a 4-day interval; H. P. edulis with a 8-day interval; I. P. edulis with a 12-day interval. Bar = 30 cm.
FIGURE 1 in Development of microsatellite loci and population genetics in the bumblebee catfish species Pseudopimelodus atricaudus and Pseudopimelodus magnus (Siluriformes: Pseudopimelodidae)
FIGURE 1 | Sampling sites of Pseudopimelodus magnus and P. atricaudus in the middle and lower sectors of the Cauca River.
Fig. 5 in Early development and allometric growth in Nannacara anomala Regan, 1905 (Perciformes: Cichlidae) under laboratory conditions
Fig. 5. Allometric growth equations between measured body proportions and total length during Nannacara anomala development. BD, body depth; ED, eye diameter; HD, head depth; HL, head length; MH, musculature height; TAL, tail length; TD, tail depth; TL, total length and TRL, trunk length. The dashed line represents the inflection point of growth.
Fig. 4 in Early development and allometric growth in Nannacara anomala Regan, 1905 (Perciformes: Cichlidae) under laboratory conditions
Fig. 4. Changes in total length (TL) from hatching to 18 days post hatch (DPH). Standard deviation (SD) represented by whiskers.
Fig. 2 in Early development and allometric growth in Nannacara anomala Regan, 1905 (Perciformes: Cichlidae) under laboratory conditions
Fig. 2. Larval development of Nannacara annomala: (a) 0 DPH, days post hatch; (b) 1 DPH; (c) 2 DPH; (d) 3 DPH; (e) 5 DPH; (f) 7 DPH; (g) 10 DPH; (h) 15 DPH; (i) 18 DPH. Scale bars = 1 mm. ag, adhesive glands; ba, branchial arches; ffv, finfold vessels; no, notochord; pfb, pelvic-fin bud; rp, rays primordia; sb, swim bladder.
Fig. 1 in Early development and allometric growth in Nannacara anomala Regan, 1905 (Perciformes: Cichlidae) under laboratory conditions
Fig. 1. Morphometric characters measured in Nannacara annomala. BD, body depth; ED, eye diameter; HD, head depth; HL, head length; MH, musculature height; TAL, tail length; TD, tail depth; TL, total length and TRL, trunk length.
Fig. 1 in Effect of water temperature and prey concentrations on initial development of Lophiosilurus alexandri Steindachner, 1876 (Siluriformes: Pseudopimelodidae), a freshwater fish
Fig. 1. Total length of Lophiosilurus alexandri after 15 days of exogenous feeding. The graph "A" and "B" showed the best temperature for the prey concentration P 700 and P 1,300, respectively.
Fig. 2 in Effect of water temperature and prey concentrations on initial development of Lophiosilurus alexandri Steindachner, 1876 (Siluriformes: Pseudopimelodidae), a freshwater fish
Fig. 2. Mean body weight of Lophiosilurus alexandri after 15 days of exogenous feeding. Different letters represent significant differences (P<0.05) among temperatures (a, b, c and d) and prey concentrations (x and y).
Figure 1 in Effect of a short-cycle apple tree cultivar on oriental fruit moth (Lepidoptera: Tortricidae) development and larval behavior
Figure 1. Average number of Grapholita molesta males captured monthly by pheromone-bait traps in 'Eva' and 'Gala' apple orchards during seven years in Porto Amazonas, Paraná, Brazil.
Figure 1 in Oncideres saga (Dalman, 1823) (Coleoptera: Cerambycidae) girdling and developing in Plathymenia reticulata Benth. (Fabaceae)
Figure 1. Plathymenia reticulata Benth. (Fabaceae) trunk girdled by Oncideres saga (Dalman, 1823) (Coleoptera: Cerambycidae) (a); and the rest of the tree, with the development of two lateral sprouts (I and II) one week (b); thirteen months after the girdling (c).
Figure 4 in Differential gene expression pattern and plasma sex steroids during testicular development in Genyatremus luteus (Perciforme: Haemulidae) (Bloch, 1790)
Figure 4. Principal component analysis (PCA) used to classify the influence of lhr and er gene expression, plasma steroids (11-KT, 17- OHP and E2), ichthyological parameters and GSI on male G. luteus individuals. Legend: LHR = LH receptor; ER = estrogen receptor; KT = 11-ketotestosterone; E2 = 17β-estradiol; OHP = 17-α-hydroxyprogesterone; TW = total weight; TL = total length; GW = gonad weight; GSI = gonadosomatic index.
Figure 1 in Differential gene expression pattern and plasma sex steroids during testicular development in Genyatremus luteus (Perciforme: Haemulidae) (Bloch, 1790)
Figure 1. Photomicrographs of germ cell and testes development stages of Genyatremus luteus. Stages were determined as (A) Immature, (B) Maturing, (C) Mature. Abbreviations are as follows: SPG, spermatogonia; SPC, spermatocyte; SPZ, spermatozoa. All panels were at 60x magnification.
Figure 2 in Differential gene expression pattern and plasma sex steroids during testicular development in Genyatremus luteus (Perciforme: Haemulidae) (Bloch, 1790)
Figure 2. Steroid concentrations in the blood plasma of male Genyatremus luteus individuals during their reproductive cycle. (A) 11-ketotestosterone. (B) 17 α-hidroxy progesterone. (C) 17β-estradiol. Data are represented as mean ± SEM. abc: indicates statistically significant difference (p<0.05).
Figure 3. B in Notes on the biological development of the darkling beetle Blaps nefrauensis nefrauensis Seidlitz, 1893 (Coleoptera: Tenebrionidae)
Figure 3. B. nefrauensis life cycle: (a) Eggs and newly hatched larva (1st instar). (b) 2nd instar larva beside eggs. (c) Larvae in the last instar. (d) Prepupa. (e) Pupa. (f) Adults. (g) Newly moulted 2ndand 4th instar larvae. (h) Moulted 2nd and 6th instar larva began to yellowish. (i) Newly moulted larva beside its old yellow cuticle. (j) Newly moulted larva compared with larva in the 8th instar. Diagram representation of the life cycle of B. nefrauensis (k).
Figure 5 in Notes on the biological development of the darkling beetle Blaps nefrauensis nefrauensis Seidlitz, 1893 (Coleoptera: Tenebrionidae)
Figure 5. Light microscopy of some structure of the newly hatched egg larva of B. nefrauensis: (a) Ligula (ventral view). (b) Lacinia teeth (ventral view). (c) Ligula, and Labial and Maxillary palpi (dorsal view). (d) Ocelli (lateral view). (e) Nerves across ligula. (f) Nerve across third antennomere. Light microscopy on the antennal protection in the embryo of B. nefrauensis (g) Larva just before egg hatching. (h) Cylindrical membrane covering apically the antennae.
Figure 4 in Notes on the biological development of the darkling beetle Blaps nefrauensis nefrauensis Seidlitz, 1893 (Coleoptera: Tenebrionidae)
Figure 4. Newly egg hatched larva: (a) First instar larva compared with egg, scale = 1 mm. (b) First instar larva compared with 8th instar larva. (c) Head (dorsal view). (d) Head (ventral view). (e-g) Pygopods and urogomphi in first instar larva
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.