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Supplementary material 1 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665
: Explanation note: Fig. S1. Effects of water extracts of desert locust frass after feeding on various plants on the numbers of egg pods laid when adult female desert locusts were presented with extracts mixed with sand.
Supplementary material 3 from: Tanaka S, Kotaki T, Nishide Y, Ben-Hamouda A, Abdellaoui K, Ebbe MAB, Ely SO (2019) Effects of water extracts of feces from three locust species and various plants on oviposition and embryonic development in the desert locust Schistocerca gregaria. Journal of Orthoptera Research 28(2): 195-204. https://doi.org/10.3897/jor.28.34665
: Explanation note: Fig. S3. Effects of water extracts of rescue grass-fed desert locust frass on antennal lengths of embryos (A, mean ± SD; n = 6–10).
Self-organized transport model of spark discharge development and its application to the process of lightning initiation in a thundercloud
<p>This video visualizes results obtained by a small-scale transport model of electrical discharge formation in a thundercloud. The model discharge tree is a dynamic graph, nodes and edges of which are capacitive and conductive elements, respectively, electrical parameters of which vary with time. In the framework of the used approach, a heated well-conducting lightning leader channel is formed by combining the currents of tens of thousands of streamers, each of which initially has a negligible conductivity and a temperature, which does not differ from the ambient value. The model leader has electrical characteristics, which are intermediate between the laboratory long spark and the developed lightning channel, which is expected for an “immature” lightning leader.</p>
Fig. 3 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)
Fig. 3 Flight and jumping muscles of Auchenorrhyncha, lateral (left) and posterior (right) views. A, B, Ricania japonica (Fulgoromorpha: Fulgoroidea: Ricaniidae); C, D, Cicadella viridis (Cicadomorpha: Membracoidea: Cicadellidae); E, F, Aphrophora pectoralis (Cercopoidea: Aphrophoridae); G, H, Graptopsaltria nigrofuscata (Cicadidae: Cicadoidea). See Fig. 2 for terminology, colors, and abbreviations. The right side of posterior images shows muscles (colored shadows) and muscle attachment regions (black dots). The border of mesophragma is highlighted by green line
Fig. 5 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)
Fig. 5 Metathoracic endoskeletons and attachment regions of IIIpcm5, lateral view. See Fig. 2 for terminology and abbreviations. a Ricania japonica (Fulgoromorpha: Fulgoroidea: Ricaniidae). b Cicadella viridis (Cicadomorpha: Membracoidea: Cicadellidae). IIIpcm5 is indicated by gray shadow. Dotted areas indicate muscle attachment regions
Fig. 4 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)
Fig. 4 Enlarged view of left metatrocanteral tendons and attachments point of muscles. a Ricania japonica (Fulgoromorpha: Fulgoroidea: Ricaniidae). b Cicadella viridis (Cicadomorpha: Membracoidea: Cicadellidae). c Aphrophora pectoralis (Cercopoidea: Aphrophoridae). d Graptopsaltria nigrofuscata (Cicadoidea: Cicadidae). See Fig. 2 for
Fig. 6 in Morphological dissection of behavior: thoracic musculature clarifies independent development of jumping mechanisms between sister groups, planthoppers and leafhoppers (Insecta: Hemiptera: Auchenorrhyncha)
Fig. 6 Most parsimonious reconstruction of character states scored in this study (Appendix) onto the phylogeny of Auchenorrhyncha estimated by Misof et al. (2014), Cryan and Urban (2012), and Urban and Cryan (2007). Out-groups are omitted. Character and character state changes reconstructed on the branches are indicated by black (gain) and white bars (reversal). For some characters (e.g., Character 5), an
Fig. 6 in Direct development in African squeaker frogs (Anura: Arthroleptidae: Arthroleptis) reveals a mosaic of derived and plesiomorphic characters
Fig. 6 Different discrete developmental events subsumed within TS 4 in Arthroleptis. a Early TS 4 of A. wahlbergii, left: close-up of head region, right: lateral view with head facing left. b Mid-TS 4 of A. wahlbergii, left: close-up of head region; right: lateral view, arrow indicates somites. c Late TS 4 of A. xenodactyloides, left: close-up of head region, forelimb buds clearly defined, right: lateral view, arrow indicates somites. Scale bars = 1 mm
Fig. 1 in Direct development in African squeaker frogs (Anura: Arthroleptidae: Arthroleptis) reveals a mosaic of derived and plesiomorphic characters
Fig. 1 Habitat (a) and clutch (b) of Arthroleptis xenodactyloides at Luhota Forest, Mufindi, Southern Udzungwas, Tanzania. c Clutch of A. wahlbergii at Entumeni Forest, KwaZulu-Natal, South Africa. Clutches were photographed in situ after the removal of covering leaves and soil
Fig. 3 in Lack of well-maintained natural history collections and taxonomists in megadiverse developing countries hampers global biodiversity exploration
Fig. 3 Correlation between the number of taxonomists and biodiversity collections in the 17 biologically megadiverse developing countries (see legend of Fig. 1 for details). Shown are the correlations between species
Fig. 2 in Lack of well-maintained natural history collections and taxonomists in megadiverse developing countries hampers global biodiversity exploration
Fig. 2 Locations of holotype deposition of 1427 newly described animal species from the 17 biologically megadiverse countries. Data including all taxa from amphipods to mammals were gathered by surveying all
Fig. 1 a –d Marine benthic organisms used for bio-optical measurements. a Boneccia viridis, b Isodictya pacmata, c Hymedesmia paupertas, d in Development of hyperspectral imaging as a bio-optical taxonomic tool for pigmented marine organisms
Fig. 1 a –d Marine benthic organisms used for bio-optical measurements. a Boneccia viridis, b Isodictya pacmata, c Hymedesmia paupertas, d Hymedesmia sp.
Fig. 10 in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 10 Diagram (a) and schematic representations (b, c) of shoot system in Pinguicula moranensis based on fig. 2c in Grob et al. (2007). Abbreviations as in Fig. 2 of the present article. b Our preferred interpretation. c Our understanding of the interpretation adopted by Grob et al. (2007)
Fig. 6 Pinguicula alpina, late flower development. a Stage with ring-shaped gynoecium primordium. b-e Flowers with calyx aestivation visible. f in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 6 Pinguicula alpina, late flower development. a Stage with ring-shaped gynoecium primordium. b-e Flowers with calyx aestivation visible. f Flower with lower lip sepals removed to show young spur of corolla. Abbreviations: g, gynoecium; pl, lower lip petals; pu, upper lip petals; s, spur, sl, lower lip sepals; su, upper lip sepals; st, stamen. Scale bars 0100 μm (a), 200 μm (b), 300 μm (e), 500 μm (c, d), 1,000 μm (f)
Fig. 1 in Inflorescence morphology and flower development in Pinguicula alpina and P. vulgaris (Lentibulariaceae: Lamiales): monosymmetric flowers are always lateral and occurrence of early sympetaly
Fig. 1 Shoots of Pinguicula alpina with different chiralities. Frontal view of shoot apices (a, c) and their diagrams (b, d). In a and b (collected 1 September 2006), eight leaves (a-h) form an anticlockwise spiral. In c and d (collected 1 September 2006), ten leaves (a-j) form a clockwise spiral. 1, 2, 3 are flowers that are formed on a shoot of preceding order. Scale bars 0500 μm. In figs. 1, 2, 3, 4, leaves and flowers of the main axis are numbered starting from the first wellvisible leaf or flower. So, in fig. 1, a number of foliage leaves preceded flowers on the main axis
Fig. 12 H. itoi, nauplius 7 in Naupliar development of Facetotecta (Crustacea: Thecostraca) and the nature of the first nauplius instar in the Crustacea - pro et contra the Hexanauplia concept
Fig. 12 H. itoi, nauplius 7, ventral side (SEM) a General view, exuvium (rupture of naupliar cuticle for y-cypris release indicated by arrowheads). b Central part with legs and labrum (endopod segments numbered in Roman, exopod segments numbered in Arabic, pores of labrum indicated by asterisks). c Posterior part. d Posteriormost end. e Armament of antenna and mandible. f Putative rudiments of frontal filaments. g Tip of labrum. Abbreviations: a1 - antennules; a2 - antennae; ba - basis; co - coxa; dap - dorsal anal plate; dcs - dorsocaudal spine; ff? - putative rudiments of frontal filaments; fs - furcal spines; lb - labrum; md - mandible; vlr – ventrolateral cuticular ridges; vmr – ventromedial cuticular ridges. Scale bars in μm
Fig. 11 H. itoi, nauplius 7 in Naupliar development of Facetotecta (Crustacea: Thecostraca) and the nature of the first nauplius instar in the Crustacea - pro et contra the Hexanauplia concept
Fig. 11 H. itoi, nauplius 7, dorsal side (SEM) a General view. b Moulting into y-cypris stage. c Head shield, left side (setae in pores indicated by arrowheads, pores without setae indicated by asterisks). d, e Posterior part of faciotrunk. f Dorsolateral view showing inner side of exuvium with 'ghost sling' of y-cypris (head shield removed). g Surface of 'ghost sling' showing delicate reticulated curicular membrane. Abbreviations: a1 - antennules; a2 - antennae; cy - y-cypris larva; dco - papilla of dorsocaudal organ; dcs - dorsocaudal spine; fs - furcal spines; gs - 'ghost sling' of y-cypris; md - mandible; n7ex - exuvium of nauplius 7; oe - cuticle of oesophagus. Scale bars in μm
Fig. 9 H. itoi, nauplius 5 in Naupliar development of Facetotecta (Crustacea: Thecostraca) and the nature of the first nauplius instar in the Crustacea - pro et contra the Hexanauplia concept
Fig. 9 H. itoi, nauplius 5, ventral side (SEM) a General view. b Left antenna and mandible (endopod segments numbered in Roman, exopod segments numbered in Arabic). c Right antennule. d Labrum (pores of labrum indicated by asterisks). e Posterior part (pores indicated by asterisks). Abbreviations: a1 - antennules; a2 - antennae; ba - basis; co - coxa; dcs - dorsocaudal spine; ff? - putative rudiments of frontal filaments; fs - furcal spines; lb - labrum; md - mandible; rmx1 - rudiments of maxillules; ob – oban; vlr – ventrolateral cuticular ridges; vmr – ventromedial cuticular ridges. Scale bars in μm
Fig. 8 H. itoi, nauplius 5 in Naupliar development of Facetotecta (Crustacea: Thecostraca) and the nature of the first nauplius instar in the Crustacea - pro et contra the Hexanauplia concept
Fig. 8 H. itoi, nauplius 5, dorsal side (SEM) a General view. b Anterior half (setae in pores indicated by arrowheads, pores without setae indicated by asterisks). c Middle-posterior part of head shield, right side (pores without setae indicated by asterisks). d Posterior part of head shield (setae in pores indicated by arrowheads, pores without setae indicated by asterisks). e Posterior part of faciotrunk. Abbreviations: bm - boundary of moult of faciotrunk; dco - papilla of dorsocaudal organ; dcs - dorsocaudal spine. Scale bars in μm
Fig. 6 H. itoi, nauplius 3 in Naupliar development of Facetotecta (Crustacea: Thecostraca) and the nature of the first nauplius instar in the Crustacea - pro et contra the Hexanauplia concept
Fig. 6 H. itoi, nauplius 3, ventral side (SEM) a General view. b Central area with labrum and naupliar legs (pores indicated by asterisk, segments of exopods numbered in Arabic, segments of endopods numbered in Roman). c Area around slit-like mouth opening (pores indicated by asterisks). d Posterior part (pore indicated by asterisk). e Anal region. Abbreviations: a1 - antennules; a2 - antennae; an - anus; ba - basis; co - coxa; dap - dorsal anal plate; dcs - dorsocaudal spine; ff? - putative rudiments of frontal filaments; fs - furcal spines; lb - labrum; md - mandible; mo - mouth opening; vlr – ventrolateral cuticular ridges; vmr – ventromedial cuticular ridges. Scale bars in μm
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.