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18,621 results for “development;”
Figure 1. Upogebia yokoyai Makarov, 1938 in The larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 (Decapoda: Gebiidea: Upogebiidae) reared under laboratory conditions
Figure 1. Upogebia yokoyai Makarov, 1938, first zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla; (H) first maxilliped; (I) second maxilliped; (J) third maxilliped; (K) pereiopods; (L) telson, dorsal view.
Figure 2. Upogebia yokoyai Makarov, 1938 in The larval development of the mud shrimp Upogebia yokoyai Makarov, 1938 (Decapoda: Gebiidea: Upogebiidae) reared under laboratory conditions
Figure 2. Upogebia yokoyai Makarov, 1938, second zoea. (A) Complete larva, dorsal view; (B) same, lateral view; (C) antennule; (D) antenna; (E) mandibles; (F) maxillule; (G) maxilla; (H) first maxilliped; (I), second maxilliped; (J), third maxilliped; (K–O), pereiopods 1–5; (P) telson, dorsal view.
Figure 2 in Reproductive behaviour and development dynamics of Odontophrynus cordobae (Anura, Cycloramphidae)
Figure 2. Courtship behaviour of Odontophrynus cordobae: (a) caller male at calling site; (b, c) submerged female approaching male and moving under his body; (d) female entirely located below the male and in physical contact with him; (e) male amplexing the female. Illustrations: L. Zavala Gallo.
Figure 1 in Reproductive behaviour and development dynamics of Odontophrynus cordobae (Anura, Cycloramphidae)
Figure 1. Release call of Odontophrynus cordobae: (a, c) oscillogram and sonogram of three calls; (b) detail of call; (d) detail of pulses.
Figure 2 in Mating behaviour, nympho-imaginal development and description of a new Mesabolivar species (Araneae: Pholcidae) from the Brazilian dry forest
Figure 2. Diagram of the sexual repertoire displayed by the Mesobolivar delclaroi sp. nov. spider. The behaviours are divided into four steps: Step I, Courtship; Step II, Pre-copulation – note in the arrow the early introduction of the copulatory bulb into the female's genitalia; Step III, Copulation, (a) lateral view, (b) ventral view – note the arrows indicating the pedipalp bristles rubbing the abdominal region of the female; Step IV, Post-copulation.
Figure 1 in Mating behaviour, nympho-imaginal development and description of a new Mesabolivar species (Araneae: Pholcidae) from the Brazilian dry forest
Figure 1. Mesabolivar delclaroi sp. nov. (A, B) Male chelicerae, (A) frontal, (B) lateral; (C) male left palp, retrolateral; (D–F) procursus tip, (D) prolateral, (E) dorsal, (F) retrolateral; (G) bulb, prolateral; (H–J) epigynum, (H) ventral, (I) lateral, (J) dorsal. Scale bar 0.5 mm.
Effects of functional depletion of doublesex on male develop-ment in the sawfly, Athalia rosae
<p><strong>Movie S3. </strong>Copulation behavior observed between a wild-type male and a diploid male obtained via complete RNAi. A single wild-type naïve male was introduced into a vial with a diploid male obtained via complete RNAi. The wild-type male successfully copulated with the <em>Ardsx</em> knockdown diploid male obtained by complete RNAi. Video recording started immediately after introducing the naïve wild-type male.</p>
Figure 8 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 8. Pictures of the preserved DNA voucher tadpole of Gephyromantis sp. aff. blanci (ZSM 649/2008). (A) Dorsal view; (B) lateral view; (C) oral disc. Note that anterior limbs have been partly removed as tissue sample for DNA barcoding.
Figure 7 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 7. Larval development of Gephyromantis sp. aff. blanci from Ranomafana. Drawings were made on the basis of photographs of living specimens and are not to scale. Time is given as days after collection of the clutch; the actual time since egg deposition is unknown. Note in the photographs in ventral view that the larvae in comparatively early stages appear to have a developed mouth with jaws (no tadpole-like oral disc).
Figure 5 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 5. Drawings of the preserved DNA voucher tadpole of Gephyromantis tschenki (ZSM 142/2007 – ZCMV 4335). (A) Dorsal view; (B) lateral view; (C) oral disc.
Figure 6 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 6. Drawings of the preserved DNA voucher tadpole of Gephyromantis ventrimaculatus (ZSM 852/2007 – ZCMV 4927). (A) Dorsal view; (B) lateral view; (C) oral disc.
Effects of functional depletion of doublesex on male develop-ment in the sawfly, Athalia rosae
<p><strong>Movie S2. </strong>Mating behavior displayed by diploid males in whom <em>Ardsx</em> expression was knocked down over an entire lifespan. Two wild-type virgin females were introduced in a vial with two diploid males obtained via complete RNAi. One of the<em> Ardsx</em> knockdown males vigorously displayed mating behavior but failed to copulate with the virgin female due to the lack of male external genitalia. Video recording started immediately after introducing the virgin wild-type female.</p>
Figure 4 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 4. Drawings of the preserved DNA voucher tadpole of Gephyromantis sculpturatus (ZSM 16/2008 – ZCMV 4833). (A) Dorsal view; (B) lateral view; (C) oral disc.
Figure 3 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 3. Colouration in life of tadpoles of three species of Gephyromantis in dorsal, lateral and ventral views. (A) G. sculpturatus (ZSM 16/2008 – ZCMV 4833); (B) G. tschenki (ZSM 142/2007 – ZCMV 4335); (C) G. ventrimaculatus (ZSM 852/2007 – ZCMV 4927). The scale bars represent 1 mm.
Figure 2 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 2. Drawings of the preserved DNA voucher tadpole of Gephyromantis granulatus (ZSM 298/2008 – Tad 2004/75). (A) Dorsal view; (B) lateral view; (C) oral disc.
Figure 1 in Nidicolous tadpoles rather than direct development in Malagasy frogs of the genus Gephyromantis
Figure 1. Photographs of the oral disc of the preserved voucher specimens of tadpoles described in this paper (stained with methylene blue). (A) Gephyromantis granulatus (ZSM 298/2008 – Tad 2004-75); (B) G. sculpturatus (ZSM 16/2008 – ZCMV 4833); (C) G. tschenki (ZSM 142/2007 – ZCMV 4335); (D) G. ventrimaculatus (ZSM 852/2007 – ZCMV 4927); (E) G. ambohitra (ZSM 756/2004 – FGMV 2003-1946); (F) G. asper (ZSM 1912/2007 – ZCMV 3401); (G) G. azzurae (ZSM 1922/2007 – T 2007-511); (H) G. corvus ZSM 0674/2008 – T 001); (I) G. pseudoasper (ZSM 707/2004 – FGMV 2003-1919). The scale bars represent 1 mm.
Figure 2 in Development rates, larval survivorship and wing length of Culex pipiens (Diptera: Culicidae) at constant temperatures
Figure 2. Temperature-dependent rate of development in male (A) and female (B) Culex pipiens from larva I until adult emergence: observed data (open circles) fitted to the Briére model (dotted line) and degree-day model (solid line).
Figure 1 in Development rates, larval survivorship and wing length of Culex pipiens (Diptera: Culicidae) at constant temperatures
Figure 1. Median (Q1–Q3) developmental time (days) of males (M) and females (F) of Culex pipiens at five constant temperatures: (A) from larva I until adult emergence; (B) for larvae IV only. Within each temperature and life stage, medians followed by different letters are significantly different (P <0.05, Mann–Whitney U -test). Numbers of individuals that emerged as male or female are indicated in parentheses.
Figure 6 in Early juvenile development of Mediterranean Liocarcinus depurator (Crustacea: Decapoda: Brachyura: Portunidae)
Figure 6. Liocarcinus depurator (Linnaeus, 1758). First crab: (A) left cheliped; (B) right cheliped; (C) pereiopod 4; (D) pereiopod 5. Measures (length and weight) in Table 1 indicated in pereiopod 5. Scale bar: 0.3 mm.
Figure 4 in Early juvenile development of Mediterranean Liocarcinus depurator (Crustacea: Decapoda: Brachyura: Portunidae)
Figure 4. Liocarcinus depurator (Linnaeus, 1758). First maxilliped. (A) first crab; (B) second crab, endopod; (C) third crab, endopod; (D) fifth crab, endopod. Second maxilliped. (E) first crab. Scale bars: 0.3 mm.
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.