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Fig. 1 in Impacts of azadirachtin and chlorantraniliprole on the developmental stages of pirate bug predators (Hemiptera: Anthocoridae) of the tomato pinworm Tuta absoluta (Lepidoptera: Gelechiidae)
Fig. 1. Longevity (days ± SE) of nymphs of Amphiareus constrictus exposed to azadirachtin and chlorantraniliprole via three routes of exposure (ingestion, residue contact and direct spray). *Comparison between two bars is statistically significant (t-test, P <0.05).
Fig. 4 in Impacts of azadirachtin and chlorantraniliprole on the developmental stages of pirate bug predators (Hemiptera: Anthocoridae) of the tomato pinworm Tuta absoluta (Lepidoptera: Gelechiidae)
Fig. 4. Proportion of nymphs of Blaptostethus pallescens that reached the adult stage afer early exposure to azadirachtin and chlorantraniliprole via three routes of exposure (ingestion, residue contact and direct spray). *Comparison between two bars is statistically significant (survival analysis/log rank test, P <0.05).
Figs. 9-15.- L I in The preimaginal stages of Carabus (Archicarabus) steuartii Deyrolle, 1852 (Coleoptera: Carabidae)
Figs. 9-15.- L I of C. steuarti. The small numbers and letters represent the diferent chetae and pores, according to the text.
Fig. 21 in The preimaginal stages of Carabus (Archicarabus) steuartii Deyrolle, 1852 (Coleoptera: Carabidae)
Fig. 21.- Head of a L I, only a few hours after hatching. The sclerotized dark egg busters are clearly visible. In the same day, the entire larva will become black-coloured.
Fig. 19.- One cleared L I in The preimaginal stages of Carabus (Archicarabus) steuartii Deyrolle, 1852 (Coleoptera: Carabidae)
Fig. 19.- One cleared L I of C. steuarti, showing the chetotaxy and the shape of the abdominal lobes.
Рис. 1–8. Barsine pulchra (Butler, 1877): 1–2 — самцы; 3 — самка; 4 — генитаΛии самца; 5 — кокон; 6 — кукоΛка; 7–8 — гусеница. Масштабная Λинейка — 5 мм Figs. 1-8. Barsine pulchra (Butler, 1877): 1–2 — male; 3 — female; 4 — male genitalia; 5 — cocoon; 6 — pupa; 7–8 — larva. Scale bar — 5 mm in The first data on preimaginal stages of Barsine pulchra (Butler, 1877) (Erebidae: Arctiinae)
Рис. 1–8. Barsine pulchra (Butler, 1877): 1–2 — самцы; 3 — самка; 4 — генитаΛии самца; 5 — кокон; 6 — кукоΛка; 7–8 — гусеница. Масштабная Λинейка — 5 мм Figs. 1-8. Barsine pulchra (Butler, 1877): 1–2 — male; 3 — female; 4 — male genitalia; 5 — cocoon; 6 — pupa; 7–8 — larva. Scale bar — 5 mm
Рис. 11. Àинамика отΛовов взросΛых (a) и моΛоΔых (b) птиц на разΛичных стаΔиях посΛебрачной и постювенаΛьной Λиньки в окрестностях пос. Гайворон в 2004–2005 гг. Fig. 11. Dynamics of catching of adult birds (a) and juvenile birds (b) at different stages of postbreeding and postjuvenile molting in the vicinity of the Gaivoron village in 2004–2005 in in the Ussuri region
Рис. 11. Àинамика отΛовов взросΛых (a) и моΛоΔых (b) птиц на разΛичных стаΔиях посΛебрачной и постювенаΛьной Λиньки в окрестностях пос. Гайворон в 2004–2005 гг. Fig. 11. Dynamics of catching of adult birds (a) and juvenile birds (b) at different stages of postbreeding and postjuvenile molting in the vicinity of the Gaivoron village in 2004–2005
Fig. 2 in Morphological and morphometric differentiation of dorsal-spined first stage larvae of lungworms (Nematoda: Protostrongylidae) infecting muskoxen (Ovibos moschatus) in the central Canadian Arctic
Fig. 2. Laboratory guide for the differentiation of L1 of U. pallikuukensis and V. eleguneniensis. The guide is based on key morphological features supported by morphometric data of heat killed L1. These features were characteristic of each of the species as visible under 400 × magnification.
Fig. 1 in Morphological and morphometric differentiation of dorsal-spined first stage larvae of lungworms (Nematoda: Protostrongylidae) infecting muskoxen (Ovibos moschatus) in the central Canadian Arctic
Fig. 1. Morphology of first stage larva (L1) of Umingmakstrongylus pallikuukensis. Photomicrograph of U. pallikuukensis L1 taken at 400 × magnification in differential interference contrast indicating the location of relevant important anatomical structures.
Fig. 3 in Morphological and morphometric differentiation of dorsal-spined first stage larvae of lungworms (Nematoda: Protostrongylidae) infecting muskoxen (Ovibos moschatus) in the central Canadian Arctic
Fig. 3. Morphology of Cystocaulus ocreatus first stage larva (L1). Photomicrograph of C. ocreatus L1 collected from Uzbekistan (US National Parasite Collection No. 95144) taken at 400 × magnification in differential interference contrast showing ventral post-anal cuticular striations and overall elongated structure of the tail spike similar to U. pallikuukensis.
Fig. 14 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 14. Phyllosoma larva of?Chelarctus sp-1, stage VII. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.
Fig. 11 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 11. Phyllosoma larva of Chelarctus crosnieri sub sp., stage V. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E, ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.
Fig. 5 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 5. Phyllosoma larva of Chelarctus virgosus, stage VI. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E, ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.
Fig. 4 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 4. Phyllosoma larva of Chelarctus virgosus, stage V. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.
Fig. 2 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 2. Neighbor-joining phylogenetic tree drawn using the Kimura-2-parameter distances for each of the partial COI sequences between the subfamily Scyllarinae species. Scyllarides brasiliensis was used as the outgroup. Closed squares indicate the phyllosoma specimens analyzed in this study. Bootstrap values of> 50% (from 1000 replicates) are shown at each node.
Fig. 1 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 1. Survey area and collection locations for the phyllosoma larvae sampled by the three research vessels: RV Shunyo-maru (SHU), Koyo-maru (KY), and RV Hakuho-maru (KH). Closed red circles indicate the sampling stations where Scyllarinae phyllosomas were collected. The specimens analyzed in this study were collected from the large circle stations. See table 1 for specimen ID.
Fig. 13 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 13. Phyllosoma larva of?Chelarctus sp-1, stage VI. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E, ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.
Fig. 3 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 3. Neighbor-joining phylogenetic tree drawn using the Kimura-2-parameter distances for each of the partial 16S rDNA sequences for species belonging to the subfamily Scyllarinae. Scyllarides brasiliensis was used as the outgroup. Closed squares indicate the phyllosoma specimens analyzed in this study. Bootstrap values of> 50% (from 1000 replicates) are shown at each node.
Fig. 7 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 7. Phyllosoma larva of Chelarctus virgosus, stage VIII. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.
Fig. 12 in Molecular Identification of Mid to Final Stage Slipper Lobster Phyllosoma Larvae of the Genus (Crustacea: Decapoda: Scyllaridae) Collected in the Pacific with Descriptions of Their Larval Morphology.
Fig. 12. Phyllosoma larva of?Chelarctus sp-1, stage V. A, ventral view; B, ventral view of eye, antennule and antenna; C, 2nd maxillule, 1st and 2nd maxilliped; D, distal end of 2nd maxilliped; E, ventral view of 1st maxillule; F, ventral view of 5th pereiopod and abdomen; G, dorsal view of 5th pereiopod and abdomen.
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.