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Fig. 4. Tetraophthalmus episcopalis Fig. 5. Amechana nobilis Fig. 6 in To The Knowledge Of Long-Horned Beetles (Coleoptera: Cerambycidae) Of The Oriental Region. Part 2.
Fig. 4. Tetraophthalmus episcopalis Fig. 5. Amechana nobilis Fig. 6. Granulorsidis (Chevrolat, 1852) Thomson, 1864 flavidosignatus Aurivillius, 1927
Fig. 10. Acronia roseolata Fig. 11. Acronia superba Fig. 12. Acronia teterevi Breuning, 1947 in To The Knowledge Of Long-Horned Beetles (Coleoptera: Cerambycidae) Of The Oriental Region. Part 1
Fig. 10. Acronia roseolata Fig. 11. Acronia superba Fig. 12. Acronia teterevi Breuning, 1947 (Breuning, 1947) Barševskis, 2016
Fig. 4. Clytellus philippinus Fig. 5. Aliboron bukidnoni Fig. 6. Gemylus albovittatus Miroshnikov & Tichy 2015 Vives, 2005 Breuning, 1960 in To The Knowledge Of Long-Horned Beetles (Coleoptera: Cerambycidae) Of The Oriental Region. Part 1
Fig. 4. Clytellus philippinus Fig. 5. Aliboron bukidnoni Fig. 6. Gemylus albovittatus Miroshnikov & Tichy 2015 Vives, 2005 Breuning, 1960
Fig. 1. Allodissus sulcatipennis Fig. 2. Hyphus lourensi Fig. 3. Clytellus benguetanus Schwarzer, 1926 Vives, 2009 Schultze, 1920 in To The Knowledge Of Long-Horned Beetles (Coleoptera: Cerambycidae) Of The Oriental Region. Part 1
Fig. 1. Allodissus sulcatipennis Fig. 2. Hyphus lourensi Fig. 3. Clytellus benguetanus Schwarzer, 1926 Vives, 2009 Schultze, 1920
Рис. 3. Спектры многоΛетней цикΛичности в разΛичных попуΛяциях Λесного Λемминга (а — ЗапаΔная ФинΛянΔия, б — Восточная ФинΛянΔия, в — АΛтай, оз. ТеΛецкое) in Long-Term Variability In Forest Lemming Population Numbers ( Liljeborg, 1844): Cyclicity
Рис. 3. Спектры многоΛетней цикΛичности в разΛичных попуΛяциях Λесного Λемминга (а — ЗапаΔная ФинΛянΔия, б — Восточная ФинΛянΔия, в — АΛтай, оз. ТеΛецкое)
Fig. 1 in Long-Term Variability In Forest Lemming Population Numbers ( Liljeborg, 1844): Cyclicity
Fig. 1. Assessment of the population dynamics of forest lemming by animal remains (Eskelinen et al. 2004)
Рис. 5. Спектр ритмов в многоΛетнем хоΔе чисΛенности Λесного Λемминга в заповеΔнике «Кивач», КареΛия (а), и в Баргузинском заповеΔнике (б) Fig. 5. The spectrum of rhythms in the long-term course of the number of forest lemming in the Kivach Reserve, Karelia (a) and in the Barguzinsky reserve (b) in Long-Term Variability In Forest Lemming Population Numbers ( Liljeborg, 1844): Cyclicity
Рис. 5. Спектр ритмов в многоΛетнем хоΔе чисΛенности Λесного Λемминга в заповеΔнике «Кивач», КареΛия (а), и в Баргузинском заповеΔнике (б) Fig. 5. The spectrum of rhythms in the long-term course of the number of forest lemming in the Kivach Reserve, Karelia (a) and in the Barguzinsky reserve (b)
Рис. 4. Спектр ритмов в многоΛетнем хоΔе чисΛенности Λесного Λемминга на КоΛьском поΛуострове (а) и в Баргузинском заповеΔнике (б) in Long-Term Variability In Forest Lemming Population Numbers ( Liljeborg, 1844): Cyclicity
Рис. 4. Спектр ритмов в многоΛетнем хоΔе чисΛенности Λесного Λемминга на КоΛьском поΛуострове (а) и в Баргузинском заповеΔнике (б)
Рис. 2. Хронограммы Δинамики попуΛяций Λесного Λемминга (а — ЗапаΔная ФинΛянΔия, б — Восточная ФинΛянΔия, в — АΛтай) in Long-Term Variability In Forest Lemming Population Numbers ( Liljeborg, 1844): Cyclicity
Рис. 2. Хронограммы Δинамики попуΛяций Λесного Λемминга (а — ЗапаΔная ФинΛянΔия, б — Восточная ФинΛянΔия, в — АΛтай)
Data and code from: Long-term climate impacts of large stratospheric water vapor perturbations
<p>The amount of water vapor injected into the stratosphere after the eruption of Hunga Tonga-Hunga Ha'apai (HTHH) was unprecedented, and it is therefore unclear what it might mean for surface climate. We use chemistry climate model simulations to assess the long-term surface impacts of stratospheric water vapor (SWV) anomalies similar to those caused by HTHH, but neglect the relatively minor aerosol loading from the eruption. The simulations show that the SWV anomalies lead to strong and persistent warming of Northern Hemisphere landmasses in boreal winter, and austral winter cooling over Australia, years after eruption, demonstrating that large SWV forcing can have surface impacts on a decadal timescale. We also emphasize that the surface response to SWV anomalies is more complex than simple warming due to greenhouse forcing and is influenced by factors such as regional circulation patterns and cloud feedbacks. Further research is needed to fully understand the multi-year effects of SWV anomalies and their relationship with climate phenomena like El Nino Southern Oscillation.</p>
Figure 2. – Maximum Likelihood phylogenetic tree inferred with the 13 in The complete mitochondrial genome of Thymallus thymallus (Linnaeus, 1758) (Actinopterygii, Salmonidae) obtained by long range PCRs and double multiplexing
Figure 2. – Maximum Likelihood phylogenetic tree inferred with the 13 protein coding genes. The values of bootstrap are represent- ed beside the nodes.
FIGURE 3. A in A long snout enchodontid fish (Aulopiformes: Enchodontidae) from the Early Cretaceous deposits at the El Chango quarry, Chiapas, southeastern Mexico: A multi-approach study
FIGURE 3. A) Lateral view of Vegrandichthys coitecus gen. et sp. nov., IHNFG 5927 holotype transferred in plastic resin from Early Cenomanian deposits of the El Chango quarry, Chiapas, Mexico. B) Artistic reconstruction of Vegrandichthys coitecus gen. et sp. nov.
FIGURE 27 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 27. Different plots of the data of the analysed long-nosed antlion larvae. A. Range of PC1 and PC2 for specimens from different time slices. For Cretaceous specimens, the grey bars provide the sample-size-corrected ranges. B. Scatter plot of head capsule width w(h) vs. capsule length l(h) (without labrum). C. PC1 and PC2 plotted against head capsule length (without labrum). Note the low degree of correlation as well as low coefficient of determination: PC1: R2=0.039, PC2: R2=0.027.
FIGURE 28 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 28. Comparison of different heads of lacewing larvae with labrum. A. Psychopsidae (MacLeod 1964, his fig. 66). B. Nevrorthidae (Beutel et al. 2010, their fig. 2). C. Myrmeleontidae (Acanthaclisis occitanica; Badano 2012, image on p. 90; re-figured in Badano et al. 2017, their fig. 7C). D. Coniopterygidae (MacLeod 1964, his fig. 62). E. Dilaridae (MacLeod 1964, his fig. 33). F. Berothidae (MacLeod 1964, his fig. 36).
FIGURE 23. Specimen 49 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 23. Specimen 49 (PED 0125); Burmese amber. A. Lateral view. B. Dorsal view. C. Lateral view, other side. D. Close-up of labrum (arrow) in dorsal view. E. Close-up of eyes in lateral view. F. Close-up of empodium (arrow) of a walking appendage. Abbreviations: at = antenna; hc = head capsule; lp = labial palp; sy = stylet; th = thorax.
FIGURE 21. Specimen 45 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 21. Specimen 45 (PED 0045); Burmese amber. A. Dorsal view. B. Dorsal view, colour marked. C. Ventral view. D. Close-up of labrum (arrow) in dorsal view. E. Close-up of labial palp. Abbreviations: at = antenna; hc = head capsule; lp = labial palp; sy = stylet; th = thorax.
FIGURE 20 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 20. Specimens in Burmese amber, continued. A–D. Specimen 43 (PED 0153). A. Dorsal view. B. Dorsal view, colour marked. C. Close-up of labrum (arrow) in dorsal view. D. Close-up of empodium (arrow) of second walking appendage. E–F. Specimen 44 (BUB 3179). E. Dorsal view. F. Dorsal view, colour marked. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; lp = labial palp; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet.
FIGURE 24 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 24. Specimens in Burmese amber, continued. A–C. Specimen 50 (PED 0039). A–C. Dorsal view. A. Ring light. B. Colour marked. C. Cross-polarised light. D. Specimen 51 (PED 0109). Abbreviations: at = antenna; hc = head capsule; sy = stylet; th = thorax.
FIGURE 17. Specimen 39 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 17. Specimen 39 (PED 0060); Burmese amber. A. Dorsal view. B. Dorsal view, colour marked. C. Ventral view. D. Close-up of antenna; arrow points to spine-like seta. E. Close-up of labrum (arrow) in dorsal view. F. Close-up of syn-inclusion, insect larva in lateral view. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet.
FIGURE 15. Specimen 37 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 15. Specimen 37 (PED 0205); Burmese amber. A. Ventral view. B. Dorsal view, colour marked. C. Dorsal view. D. Close-up of antenna; arrow points to spine-like seta. E. Close-up of labrum (arrow) in dorsal view. F. Close-up of empodium (arrow) of second walking appendage. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet; ta = tarsus; ti = tibia.
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.