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FIGURE 23 in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 23. Cladochaeta grimaldii, nov. sp., holotype, male terminalia. A, C. Terminal oblique view. B, D. Lateral view.
FIGURE 16 in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 16. Cladochaeta chauliodactyla nov. sp., holotype, male terminalia. A, D. Terminal view. B, E. Terminal oblique view. C, F. Lateral view.
FIGURE 25 in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 25. Cladochaeta atlantica nov. sp., paratype, male terminalia. A. Terminal view. B. Lateral view. C. Lateral view of the complex of aedeagus and paraphyses.
FIGURE 11. Cladochaeta arthrostyla A. Head, dorsal view. B. Head, lateral view. C. Head, frontal view. D. Thorax, lateral view. E. Thorax, dorsal view. F in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 11. Cladochaeta arthrostyla A. Head, dorsal view. B. Head, lateral view. C. Head, frontal view. D. Thorax, lateral view. E. Thorax, dorsal view. F. Abdomen, dorsal view. Scale bars: 0.1mm.
FIGURE 5 in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 5. Cladochaeta balbiae nov. sp., holotype, male terminalia. A, D. Terminal view. B, E. Terminal oblique view. C, F. Lateral view.
FIGURE 15 in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 15. Cladochaeta chauliodactyla nov. sp., holotype. A. Head, dorsal view. B. Head, lateral view. C. Head, frontal view. D. Thorax, lateral view. E. Thorax, dorsal view. F. Dorsal view of Abdomen. Scale bars: 0.1mm.
FIGURE 4 in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 4. Cladochaeta balbiae nov. sp., holotype. A. Head, dorsal view. B. Head, lateral view. C. Head, frontal view. D. Thorax, lateral view. E. Thorax, dorsal view. F. Abdomen, dorsal view. Scale bars: 0.1mm.
FIGURE 9. Cladochaeta bomplandi. A. Head, dorsal view. B. Head, lateral view. C. Head, frontal view. D. Thorax, lateral view. E in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 9. Cladochaeta bomplandi. A. Head, dorsal view. B. Head, lateral view. C. Head, frontal view. D. Thorax, lateral view. E. Thorax, dorsal view. Scale bars: 0.1mm.
FIGURE 8 in Going beyond the tip of the Drosophilidae iceberg: New Cladochaeta Coquillett, 1900 (Diptera: Drosophilidae) from Brazil
FIGURE 8. Cladochaeta paraitinga nov. sp., holotype, male terminalia. A, B. Lateral view. C. Terminal view. D. Lateral view of phallus.
Accompanying simulated data for "Go multivariate: recommendations on multilevel hidden Markov models with categorical data of varying complexity"
<p>The multilevel hidden Markov model (MHMM) is a promising vehicle to investigate latent dynamics over time in social and behavioral processes. By including continuous individual random effects, the model accommodates variability between individuals, providing individual-specific trajectories and facilitating the study of individual differences. However, the performance of the MHMM has not been sufficiently explored. Currently, there are no practical guidelines on the sample size needed to obtain reliable estimates related to categorical data characteristics We performed an extensive simulation to assess the effect of the number of dependent variables (1-4), the number of individuals (5-90), and the number of observations per individual (100-1600) on the estimation performance of group-level parameters and between-individual variability on a Bayesian MHMM with categorical data of various levels of complexity. We found that using multivariate data generally alleviates the sample size needed and improves the stability of the results. Regarding the estimation of group-level parameters, the number of individuals and observations largely compensate for each other. Meanwhile, only the former drives the estimation of between-individual variability. We conclude with guidelines on the sample size necessary based on the complexity of the data and the study objectives of the practitioners.</p> <p>This repository contains data generated for the manuscript: "Go multivariate: recommendations on multilevel hidden Markov models with categorical data of varying complexity". It comprehends: (1) model outputs (maximum a posteriori estimates) for each repetition (n=100) of each scenario (n=324) of the main simulation, (2) complete model outputs (including estimates for 4000 MCMC iterations) for two chains of each repetition (n=3) of each scenario (n=324). Please note that the empirical data used in the manuscript is not available as part of this repository. A subsample of the data used in the empirical example are openly available as an example data set in the R package <a href="https://cran.r-project.org/web/packages/mHMMbayes/index.html">mHMMbayes on CRAN</a>. The full data set is available on request from the authors.</p>
Experimental results for the Power on the go problem
<p>There are 8 .xlsx files in total: 4 for single drop and 4 for double drop. These include the results for both the uniform and normal distributions generated by the MILP solver, and the results of the All and Hybrid heuristic.</p>
Figure 14 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 14. Summary of the main structures related with apneustic respiratory system. A–C, Berosus decolor Knisch, 1924, light microscope photograph: A, habitus, first-instar larva, dorsal view; B; terminal spiracle, third-instar larva, dorsal view; C; detail of the abdominal spiracular trachea and tracheal gill, dorsal view. D, Berosus pallipes Brullé, 1841, abdominal spiracle, third-instar larva, dorsal view. E–H, Berosus sp., third-instar larva, SEM micrograph: E, spiracular chamber, ventral view; F; first abdominal segment bearing tracheal gill, dorsal view; G, detail of tracheal gill surface; H, abdominal spiracle. I, J, Hemiosus bruchi Knisch, 1924, third-instar larva, SEM micrograph: I, last abdominal segments, dorsal view; J, abdominal spiracle. K, Hemiosus multimaculatus (Jensen-Haarup, 1910), spiracular chamber, third-instar larva, ventral view.
Figure 15 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 15. Phylogeny of the Hydrophiloidea with mapped evolution of tracheal system (A) and mouthparts (B, C). Two alternative ancestral state reconstructions of mouthparts, considering mouthparts of the Pelthydrus-group as: B, piercingsucking; C, chewing (only tribe Laccobiini shown). D, number of species of aquatic genera of Hydrophilidae with known larvae. Colors of branches/bars/pie-charts indicate functional morphology of mouthparts (red = piercing-sucking, blue = chewing, green = filter-feeding) and development of the tracheal system (grey = open; orange = closed).
Figure 12 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 12. Schematic drawing of the piercing-sucking feeding mechanism: 1, sucking channel; 2, epistomal-mandibular coupling system; 3, flexible area.
Figure 13 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 13. Summary of the main structures related with metapneustic respiratory system. A, Tropisternus latus (Brullé, 1837), spiracular chamber, first-instar larva, light microscope photograph, dorsal view. B, Helochares ventricosus Bruch, 1915, spiracular chamber, first-instar larva, light microscope photograph, dorsal view. C, Tropisternus latus (Brullé, 1837), spiracular chamber, first-instar larva, light microscope photograph, dorsal view. D, Helochares ventricosus Bruch, 1915, abdominal spiracle, first-instar larva, light microscope photograph, dorsal view. E–H, Tropisternus setiger Germar, 1824, SEM micrograph: E, spiracular chamber, third-instar larva, ventral view; F, detail of the terminal spiracle with dust filter, third-instar larva, ventral view; G, abdominal spiracle, first-instar larva, dorsal view; H, detail of the closed abdominal spiracles, first-instar larva, dorsal view. I, J, Oocyclus iguazu (Oliva 1996) third-instar larva, SEM micrograph: I, spiracular chamber, dorsal view; J, biforous abdominal spiracle, dorsal view. K, Laccobius kunashiricus Shatrovskiy, 1984, spiracular chamber, third-instar larva, SEM micrograph, dorsal view.
Figure 11 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 11. Summary of the main structures related with piercing-sucking feeding mechanism, SEM micrograph. A, B, Berosus sp., third-instar larva: A, lobular-mandibular coupling system, dorsal view; B, detail of lobular-mandibular coupling system, ventral view. C, Laccobius (Microlaccobius) sp., third-instar larva, left epistomal lobe, dorsal view.
Figure 10 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 10. Frame sequences of videos showing feeding behavior. A, Tropisternus latus Brullé, 1837, note that the larvae raise the head out of water while feeding. B, Hydrophilus (Dibolocelus) palpalis Brullé, 1837. C, Hemiosus dejeanii (Solier, 1849). D, Oocyclus magnifica Hebauer & Wang, 1998. See also Supporting Information, Videos S1–S4.
Figure 5 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 5. Labroclypeal region of larvae with chewing feeding system, SEM micrograph, dorsal view. A, Tropisternus acaragua Bachmann, 1969, first-instar larva. B, Hydrochara caraboides (Linnaeus, 1758), first-instar larva. C, Hydrophilus (Dibolocelus) palpalis Brullé, 1837, second-instar larva. D, Derallus paranensis Oliva, 1981, first instar larva. E, Helochares ventricosus Bruch, 1915, first-instar larva. F, Hydroglobus puncticolle Bruch, 1915, third-instar larva. G, Dactylosternum cacti (LeConte, 1855), third-instar larva. H, Cercyon quisquilius (Linnaeus, 1761), third-instar larva, white arrow indicates labroclypeal notch. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
Figure 1 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 1. Head capsule of larvae with chewing (A–C) and piercing-sucking (D–I) feeding system, SEM micrograph, dorsal view. A, Hydrophilus (Dibolocelus) palpalis Brullé, 1837, second-instar larva. B, Tropisternus setiger Germar, 1824, firstinstar larva. C, Derallus paranensis Oliva, 1981, first instar larva. D, Berosus sp., third-instar larva. E, Hemiosus bruchi Knisch, 1924, third-instar larva. F, Oocyclus iguazu (Oliva 1996), third-instar larva. G, Laccobius kunashiricus Shatrovskiy, 1984, third-instar larva. H, Hybogralius hartmeyeri (Régimbart, 1908), third-instar larva, light microscope photograph. I, Epimetopus mendeli Fikáček et al. 2011, first-instar larva.
Figure 6 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 6. Labroclypeal region of Hemiosus larvae. A, B, Hemiosus bruchi Knisch, 1924, third-instar larva, SEM micrograph, dorsal view: A, labroclypeus; B, left epistomal lobe. C–E, Hemiosus multimaculatus (Jensen-Haarup, 1910), third-instar larva, dorsal view: C, left epistomal lobe, SEM micrograph; D, detail of gFR2 serrated setae, SEM micrograph; E, left epistomal lobe, light microscope photograph. Abbreviations: EpLb, epistomal lobe; NS, nasale. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
ScienceDex guides
Understand access before you commit
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.