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FIGURE 14. Specimen 36 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 14. Specimen 36 (PED 0137); 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 empodium (arrow) of second walking appendage. Abbreviations: ad = abdomen; at = antenna; cl = claw; hc = head capsule; lp = labial palp; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet.
FIGURE 26 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 26. Scatterplot of PC1 and PC2 surrounded by all analysed heads. Numbers in the ellipses correspond to the numbers of the heads. Extant specimens as grey ellipses, Eocene specimens as white ellipses, Cretaceous specimens as black ellipses. The heads grouped together in circles cluster relatively closely together and possibly form relatively discrete types.
FIGURE 22 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 22. Specimens in Burmese amber, continued. A–C Specimen 46 (PED 0133). A. Ventral view. B. Dorsal view, colour marked; arrow points to labrum. C. Dorsal view. D–F. Specimen 47 (PED 0128). D. Ventral view. E. Dorsal view, colour marked; arrow points to labrum. F. Dorsal view. G–H. Specimen 48 (BUB 3386). G. Dorsal view. H. Dorsal view, slightly different angle; arrow points to labrum. Abbreviations: at = antenna; hc = head capsule; lp = labial palp; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet.
FIGURE 7. Specimen 16 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 7. Specimen 16 (IGR.ARC-205.2); Charentese amber. A. Ventral view. B. Dorsal view. C. Dorsal view, colour marked. D. Close-up of labrum (arrow) in ventral view. E. Close-up of antenna in dorsal view; arrow points to spine-like seta. F. Close-up of empodium (arrow) of first walking appendage. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet.
FIGURE 3 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 3. Fossils of long-nosed antlion larvae, i.e., larvae of silky lacewings (Psychopsidae), continued. Drawings partly simplified. A. Specimen 15, from Weitschat and Wichard (1998, 2002). B. Specimen 17, from Scheven (2004). C. Specimen 18, from Engel and Grimaldi (2008). D. Specimen 19, from Gröhn (2015). E. Specimen 20, from Zhang (2017). F. Specimen 21, from Badano et al. (2018). G. Specimen 22, from Makarkin (2018). H. Specimen 23, from Makarkin (2018).
FIGURE 6 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 6. Specimens in Baltic amber, continued. A. Specimen 26 (Gröhn 7507), ventral view, strongly verlumt. B. Specimen 27; image from Jonas Damzen. C. Specimen 28. D. Specimen 29. E. Specimen 30. C–E. Images by Marius Veta.
FIGURE 1 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 1. All known extant long-nosed antlion larvae, i.e., larvae of silky lacewings (Psychopsidae). Drawings partly simplified. A. Specimen 1, from Froggatt (1907). B–E. All from Tillyard (1918). B1. Specimen 2. B2. Specimen 2 in the same scale as the other specimens from Tillyard (1918). C. Specimen 3. D. Specimen 4. E. Specimen 5. F. Specimen 6, from Withycombe (1925). G. Specimen 7, from Macleod (1964). H. Specimen 8, from New (1989). I. Specimen 9, from New (1991). J. Specimen 10, from Aspöck and Aspöck (1999). K. Specimen 11, from Badano et al. (2017). L. Specimen 12, from Bakkes et al. (2017).
FIGURE 9. Specimen 31 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 9. Specimen 31 (BUB 3356); Burmese amber. A. Dorsal view. B. Dorsal view, colour marked. C. Close-up of labrum (arrow) in ventral view. D. Ventral view. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; lp = labial palp; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet.
FIGURE 8. Specimen 16 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 8. Specimen 16 (IGR.ARC-205.2), continued. A–B. Composite fluorescence images in dorsal view, note the surface details. A. Blue light (GFP). B. Green light (TRITC). C. Composite bright-field image.
FIGURE 10. Specimen 32 in The decline of silky lacewings and morphological diversity of long-nosed antlion larvae through time
FIGURE 10. Specimen 32 (PED 0055); 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 empodium (arrow) of third walking appendage. F. Close-up of abdomen. Abbreviations: ad = abdomen; at = antenna; hc = head capsule; lp = labial palp; ms = mesothorax; mt = metathorax; pt = prothorax; sy = stylet.
Figure 7 in Long - term variations in macrobenthos diversity at the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 7. Shannon (H′) & evenness (J) indices for T. stroemi - A. stepanovi communities at the Bosporus outlet area (depth 70 - 98 m – 1958, depth 96 - 152 m - 2010*) - (A); & M. phaseolina (depth 83-113м -1960, depths 116-117 м - 2010*)-(B) communities at the Bosporus outlet area.
Figure 2 in Long - term variations in macrobenthos diversity at the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 2. Dependence of the abundance and species richness of the benthos in the Bosporus outlet area on water depth and on the dissolved-oxygen concentration measured just above the sediment: RV 'Maria S. Merian' 15/1, April-May 2010.
Figure 1 in Long - term variations in macrobenthos diversity at the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 1. Macrobenthos sampling stations in the Istanbul Strait"s (Bosporus) outlet area of the Black Sea (RV 'Maria S. Merian' 15/1, April-May 2010) – (a), July 1958 and June 1960 RV "Academic Kovalevsky" cruises in the Bosporus area – (b).
Figure 6 in Long - term variations in macrobenthos diversity at the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 6. Simpson (D) & Berger-Parker (B\P) indices for T. stroemi – A, stepanovi *) - (A); & M. phaseolina (depth 83-113м -1960, depths 116-117 м - 2010*)-(B) communities at the Bosporus outlet area.
Figure 4 in Long - term variations in macrobenthos diversity at the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 4. Plots of log-normal model for T. stroemi – A. stepanovi (depth 70 - 98 m – 1958, depth 96 - 152 m - 2010*) - (a); M. phaseolina communities (depth 83-113м -1960, depths 116-117 м - 2010*)-(b): (y axis) - cumulative % of species against (x axis) - individuals per species in geometric classes.
Figure 8 in Long - term variations in macrobenthos diversity at the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 8. Menhinick (DMn) & Margalef (DMG) indices for T. stroemi – A. stepanovi (depth 70 - 98 m – 1958, depth 96 - 152 m - 2010*) *) - (A); & M. phaseolina (depth 83-113м -1960, depths 116-117 м - 2010*)-(B) communities at the Bosporus outlet area.
Figure 5 in Long - term variations in macrobenthos diversity at the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 5. Structure of density for T. stroemi – A. stepanovi (depth 70 - 98 m – 1958, depth 96 - 152 m - 2010*) - (a); & M. phaseolina communities (depth 83-113м -1960, depths 116-117 м - 2010*)-(b).
Density dependence maintains long-term stability despite increased isolation and inbreeding in the Florida Scrub-Jay
<p>Isolation caused by anthropogenic habitat fragmentation can destabilize populations. Populations relying on the inflow of immigrants can face reduced fitness due to inbreeding depression as fewer new individuals arrive. Empirical studies of the demographic consequences of isolation are critical to understanding how populations persist through changing conditions. We used a 34-year demographic and environmental dataset from a population of cooperatively-breeding Florida Scrub-Jays (<em>Aphelocoma coerulescens</em>) to create mechanistic models linking environmental and demographic factors to population growth rates. We found that the population has not declined despite both declining immigration and increasing inbreeding, owing to a coinciding response in breeder survival. We find evidence of density-dependent immigration, breeder survival, and fecundity, indicating that interactions between vital rates and local density play a role in buffering the population against change. Our study elucidates the impacts of isolation on demography and how long-term stability is maintained via demographic responses.</p>
Figure 5 in Hydrogen peroxide is involved in drought stress long-distance signaling controlling early stomatal closure in tomato plants
Figure 5. Growth analysis of shoots and roots of tomato BS II0020 grown under irrigated or drought conditions. (A) fresh weight; (b) dry weight; (c) foliar area; (d) height. Control plants received full irrigation throughout the experiment. The values are the means of each treatment (n= 4), followed by the standard error. The letters over the bars represent the differences in the means between biochemical treatments within each condition, and the asterisks the differences of the same biochemical treatment between the conditions, calculated by Scott-knott test at 5% probability.
Figure 4 in Hydrogen peroxide is involved in drought stress long-distance signaling controlling early stomatal closure in tomato plants
Figure 4. Open stomata (a) and water loss by detached leaves (b) of tomato BS II0020. The values are the means of each treatment (n= 4), followed by the standard error. The letters over the bars represent the differences in the means among biochemical treatments within each condition, and the asterisks the differences of the same biochemical treatment between the conditions, calculated by Scott-knott test at 5% probability.
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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.