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Maintenance of a narrow hybrid zone between native and introduced red foxes (Vulpes vulpes) despite conspecificity and high dispersal capabilities
<p>Human-facilitated introductions of nonnative populations can lead to secondary contact between previously allopatric lineages, resulting in either homogenization of the lineages or stable hybrid zones that are maintained by pre-zygotic (e.g., behavioral) or post-zygotic (e.g., reduced hybrid fitness) reproductive barriers. We investigated patterns of gene flow between the native Sacramento Valley red fox (<em>Vulpes vulpes patwin</em>) and an introduced conspecific population of captive-bred (fur-farm) origin in California's Central Valley. Considering their recent divergence (i.e., ~50 kya), we hypothesized that pre-zygotic mechanisms primarily impede gene flow, rather than post-zygotic barriers. Additionally, some genes originating in nonnative foxes may confer higher fitness in the currently human-dominated landscape resulting in selective introgression into the native population. Genetic analysis of 682 red foxes (255 native, 427 nonnative) at both mitochondrial (cytB + Dloop) and nuclear loci (~19,000 SNPs) revealed significantly narrower cline widths than expected under a simulated model of unrestricted gene flow, consistent with the existence of pre- or post-zygotic reproductive barriers. We identified several loci with reduced introgression linked to behavioral divergence in captive bred foxes, which supports pre-zygotic mechanisms as a putative driver of the narrow hybrid zone. Additionally, several loci with elevated gene flow from the nonnative into the native population, were near genes associated with adaptation to human dominated landscapes. Overall, this study contributes to our understanding of hybrid zone dynamics in vertebrates, particularly in the context of species introductions and landscape changes, underscoring the importance of considering multiple mechanisms that may be at play in maintaining lineages at both the species and subspecies level.</p>
Figure 3 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 3. The overall effect of narrow row spacing (<76 cm) on weed density, weed biomass,weed control,weed seed production,and crop yield.The vertical black dashed line indicates zero effect. The black dots represent mean effect sizes (log of response ratios [lnðRRÞ]), and the black lines represent their respective 95% confidence intervals (CIs). The numbers in parentheses indicate the number of observations followed by the number of studies for each effect size. The effect sizes were considered significantly different when their 95% CIs did not overlap or contain zero.
Figure 6 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 6. The effect of narrow row spacing (<76 cm) on crop yield as explained by subgroups of the crop, tillage, weed type, weed management method, herbicide application frequency, and time. The vertical black dashed line indicates zero effect. The black dots represent mean effect sizes (log of response ratios [lnðRRÞ]) for each subgroup, and the black lines represent their respective 99% confidence intervals (CIs). The numbers in parentheses indicate the number of observations followed by the number of studies for each effect size. The effect sizes were considered significantly different when their 99% CIs did not overlap or contain zero.
Figure 2. A in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 2. A map of the states in the midwestern and eastern United States showing experimental sites for the 35 corn and soybean narrow row spacing studies included in the meta-analysis.
Figure 5 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 5. The individual effect sizes (natural log of response ratios [lnðRRÞ]) of (A) weed density, (B) weed biomass,(C) weed control, (D) weed seed production, and (E) crop yield as a function of crop row spacing. The green and red dots represent individual effect sizes for corn and soybean, respectively. The horizontal black dashed line represents zero effect,while the vertical black line represents 76-cm row spacing (control).The black bold line shows the relationship between individual effect sizes and crop row spacing,which is given as R (Pearson's correlation) with a P-value. The gray-shaded area represents 95% confidence intervals (CIs) of the linear relationship.
Figure 8 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 8. Sensitivity analysis showing the variation in overall effect sizes (log of response ratios [ln(RR)]) (mean ± 95% confidence intervals [CIs]) of narrow row spacing effects on (A) weed density, (B) weed biomass, (C) weed control, (D) weed seed production, and (E) crop yield when any specific study was excluded from the analysis. The vertical red solid and dashed lines represent the mean ± 95% CIs, respectively, of overall effect sizes with all the studies included in the analysis.
Figure 1 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 1. PRISMA (Preferred Reporting Items for Systematic Reviews and MetaAnalyses; Page et al. 2021) flow diagram showing the stepwise procedure used for selecting 35 studies for meta-analysis.
Figure 4 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 4. The effect of narrow row spacing (<76 cm) on (A) weed density, (B) weed biomass, (C) weed control, and (D) weed seed production as explained by the subgroups of crop,tillage,weed type,weed management method, herbicide application frequency, and time. The vertical black dashed line indicates zero effect.The black dots represent mean effect sizes (log of response ratios [lnðRRÞ]) for each subgroup, and the black lines represent their respective 99% confidence intervals (CIs). The numbers in parentheses indicate the number of observations followed by the number of studies for each effect size. The effect sizes were considered significantly different when their 99% CIs did not overlap or contain zero.
Figure 7 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis
Figure 7. Density plots show the distribution of individual effect sizes (log of response ratios [ln(RR)]) of weed density,biomass,control, weed seed production, and crop yield.
Toward liquid cell quantum sensing: Ytterbium complexes with ultra-narrow absorption
<p>The energetic disorder induced by fluctuating liquid environments acts in opposition to the precise control required for coherence-based sensing. Overcoming fluctuations requires a protected quantum subspace that only weakly interacts with the local environment. We reported a ytterbium complex that exhibited an ultra-narrow absorption linewidth in solution at room temperature with a full-width at half-maximum of 0.625 meV. Using spectral hole-burning, we measured an even narrower linewidth of 410 peV at 77 K. Narrow linewidths allowed low-field magnetic circular dichroism at room temperature, used to sense Earth-scale magnetic fields. These results demonstrated that ligand protection in lanthanide complexes could significantly diminish electronic state fluctuations. We termed this system an 'atom-like molecular sensor' (ALMS) and proposed approaches to improve its performance.</p>
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main
Dataset for "Tidal control of the flow through long, narrow straits: a modeling study for the Seto Inland Sea"
<p>This dataset contains simulated results used to draw figures in the following paper.</p> <p>Kurogi, M. & Hasumi, H. Tidal control of the flow through long, narrow straits: a modeling study for the Seto Inland Sea, Sci. Rep. 9, 11077 (2019).</p> <p>==== List of data</p> <p> dep_T.nc: Depth of tracer point<br> dep_V.nc: Depth of velocity point<br> ssh.nc: Sea Surface Height for TIDE (hourly snapshots of July 2012)<br> ubt_TIDE.nc: Eastward barotropic velocity for TIDE (monthly mean)<br> vbt_TIDE.nc: Northward barotropic velocity for TIDE (monthly mean)<br> ubt_NTIDE.nc: Eastward barotropic velocity for NTIDE (monthly mean)<br> vbt_NTIDE.nc: Northward barotropic velocity for NTIDE (monthly mean)<br> ubt_NTIDE_DV0.nc: Eastward barotropic velocity for NTIDE_DV0 (monthly mean)<br> vbt_NTIDE_DV0.nc: Northward barotropic velocity for NTIDE_DV0 (monthly mean)<br> ubt_NTIDE_D.nc: Eastward barotropic velocity for NTIDE_D (monthly mean)<br> vbt_NTIDE_D.nc: Northward barotropic velocity for NTIDE_D (monthly mean)<br> ubt_NTIDE_DV.nc: Eastward barotropic velocity for NTIDE_DV (monthly mean)<br> vbt_NTIDE_DV.nc: Northward barotropic velocity for NTIDE_DV (monthly mean)<br> ubt_NTIDE_DVA.nc: Eastward barotropic velocity for NTIDE_DVA (monthly mean)<br> vbt_NTIDE_DVA.nc: Northward barotropic velocity for NTIDE_DVA (monthly mean)<br> ubt_inout.nc: Eastward barotropic velocity for the inflow-outflow model (monthly mean)<br> vbt_inout.nc: Northward barotropic velocity for the inflow-outflow model (monthly mean)<br> amv_TIDE.nc: Vertical average of vertical viscosity for TIDE (monthly mean)<br> ahv_TIDE.nc: Vertical average of vertical diffusivity for TIDE (monthly mean)<br> amv_NTIDE.nc: Vertical average of vertical viscosity for NTIDE (monthly mean)<br> ahv_NTIDE.nc: Vertical average of vertical diffusivity for NTIDE (monthly mean)<br> ke.nc: Vertical average of kinetic energy per unit mass for TIDE (monthly mean)<br> ke_bt.nc: Vertical average of barotropic kinetic energy per unit mass for TIDE (monthly mean)</p> <p> </p>
Text-fig. 9. Revultex impression of a siliceous concretion NM L 31967. A – an assemblage of three specimens of Barrandicella cf. tarda (PERNER, 1903); a – indeterminate early shell (? Barrandicella sp.), b – Mytoconula sp., ×...... B – Mytoconula sp., obligue left lateral view of an early shell just after landing on the Barrandicella surface, with a narrow flat rim of initial teleoconch shell, probably pressed down by sediment, ×......; C – the same, obligue left lateral view, ×......; D – the same, oblique right posterolateral view showing increments in the early shell, ×....... Dobrotivá F., PrahaŠárka. in Patelliconus Horný, 1961 And Mytoconula Gen. N. (Mollusca, Tergomya) From The Ordovician Of Perunica
Text-fig. 9. Revultex impression of a siliceous concretion NM L 31967. A – an assemblage of three specimens of Barrandicella cf. tarda (PERNER, 1903); a – indeterminate early shell (? Barrandicella sp.), b – Mytoconula sp., ×...... B – Mytoconula sp., obligue left lateral view of an early shell just after landing on the Barrandicella surface, with a narrow flat rim of initial teleoconch shell, probably pressed down by sediment, ×......; C – the same, obligue left lateral view, ×......; D – the same, oblique right posterolateral view showing increments in the early shell, ×....... Dobrotivá F., PrahaŠárka.
Figure 20. Presumed Rufousbacked Robin Turdus rufopalliatus graysoni with mainly narrow throat streaks, a in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?
Figure 20. Presumed Rufousbacked Robin Turdus rufopalliatus graysoni with mainly narrow throat streaks, a strong salmon wash on the breast, and wing-coverts and back colours close to those of non-graysoni T. rufopalliatus, Isla María Cleofas, November 2015 (Javier Cruz Nieto)
Reproduction package for the article "Accretion disc cooling and narrow absorption lines in the tidal disruption event AT 2019dsg"
<p>This is the reproduction package for the MNRAS Article "Accretion disc cooling and narrow absorption lines in the tidal disruption event AT 2019dsg" by Cannizzaro et al (2021). It contains the reduced optical data, the scripts used for the emission lines fitting and the code used to perform the host galaxy subtraction.</p>
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i).
Text-fig. 46. Scanning electron microscope (SEM) images of monocolpate pollen of Teebacia hughesii gen. et sp. nov. pollen from a stamen fragment; Torres Vedras locality, Portugal. a) Holotype; stamen fragment showing elongated pollen sacs that yielded the pollen in this Text-figure (d, e); b) Detail of detached reticulum showing inner surface of muri and scattered columellae; note the finely granular covering of the muri and columellae; c, d) Detail of reticulum showing the outer surface of muri with supratectal ornamentation of narrow ridges; note orbicules attached to the reticulum (d); e, f) Pollen grains showing loose, beaded, reticulum with long columellae; note continuous muri bordering the apertures and densely spaced minute orbicules lining the inner surface of the anther wall (e, arrowheads). Specimens, TV44-S136666 (holotype; a, d, e), TV44-S149207 (b, c, f). Scale bars 300 Μm (a), 6 Μm (e, f), 3 Μm (b), 1.5 Μm (c), 1.2 Μm (d). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 46. Scanning electron microscope (SEM) images of monocolpate pollen of Teebacia hughesii gen. et sp. nov. pollen from a stamen fragment; Torres Vedras locality, Portugal. a) Holotype; stamen fragment showing elongated pollen sacs that yielded the pollen in this Text-figure (d, e); b) Detail of detached reticulum showing inner surface of muri and scattered columellae; note the finely granular covering of the muri and columellae; c, d) Detail of reticulum showing the outer surface of muri with supratectal ornamentation of narrow ridges; note orbicules attached to the reticulum (d); e, f) Pollen grains showing loose, beaded, reticulum with long columellae; note continuous muri bordering the apertures and densely spaced minute orbicules lining the inner surface of the anther wall (e, arrowheads). Specimens, TV44-S136666 (holotype; a, d, e), TV44-S149207 (b, c, f). Scale bars 300 Μm (a), 6 Μm (e, f), 3 Μm (b), 1.5 Μm (c), 1.2 Μm (d).
Text-fig. 42. Scanning electron microscope (SEM) images of monocolpate pollen of Piercipollis sp. 1 (a–c) from an isolated anther and Piercipollis sp. 2 (d–f) from a coprolite (not shown); Torres Vedras locality, Portugal. a) Narrow elongate anther that yielded the pollen in (b) and (c); b) Distal view of pollen grain showing well-developed reticulum that is only loosely attached to the foot layer; note the smooth foot layer (arrowhead) of a grain from which the reticulum has become detached; c) Reticulum showing the smooth muri and long columellae that are mostly detached from the foot layer; d–f) Pollen grains in distal (d, e), and lateral views (f) showing the very long colpus and the well-developed reticulum only loosely attached to the smooth surface of the foot layer; note the main body of the grains (foot layer) does not fill out the whole space of the reticulum (f). Specimens, TV44-S148218 (a–c), TV142-S170216 (d–f). Scale bars 300 Μm (a), 6 Μm (b, d–f), 3 Μm (c). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 42. Scanning electron microscope (SEM) images of monocolpate pollen of Piercipollis sp. 1 (a–c) from an isolated anther and Piercipollis sp. 2 (d–f) from a coprolite (not shown); Torres Vedras locality, Portugal. a) Narrow elongate anther that yielded the pollen in (b) and (c); b) Distal view of pollen grain showing well-developed reticulum that is only loosely attached to the foot layer; note the smooth foot layer (arrowhead) of a grain from which the reticulum has become detached; c) Reticulum showing the smooth muri and long columellae that are mostly detached from the foot layer; d–f) Pollen grains in distal (d, e), and lateral views (f) showing the very long colpus and the well-developed reticulum only loosely attached to the smooth surface of the foot layer; note the main body of the grains (foot layer) does not fill out the whole space of the reticulum (f). Specimens, TV44-S148218 (a–c), TV142-S170216 (d–f). Scale bars 300 Μm (a), 6 Μm (b, d–f), 3 Μm (c).
Text-fig. 39. Scanning electron microscope (SEM) images of monocolpate pollen of Eckhartia intermedia sp. nov. from a pollen clump, probably fragment of a stamen (a–e) and anthers and pollen of Eckhartia sp. (f–k); Torres Vedras locality, Portugal. a) Pollen clump that yielded the pollen in (b–e); b–d) Pollen grains viewed from distal (d) and proximal surfaces (b, c) showing the long colpus and well-developed reticulum with large and small luminae; e) Reticulum showing smooth muri supported by short columellae firmly attached to the smooth surface of the foot layer; note the occasional small luminae; f, g) Fragments of narrow elongate anthers with same kind of pollen as in (i); h) Inner surface of anther wall showing small spherical orbicules; in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 39. Scanning electron microscope (SEM) images of monocolpate pollen of Eckhartia intermedia sp. nov. from a pollen clump, probably fragment of a stamen (a–e) and anthers and pollen of Eckhartia sp. (f–k); Torres Vedras locality, Portugal. a) Pollen clump that yielded the pollen in (b–e); b–d) Pollen grains viewed from distal (d) and proximal surfaces (b, c) showing the long colpus and well-developed reticulum with large and small luminae; e) Reticulum showing smooth muri supported by short columellae firmly attached to the smooth surface of the foot layer; note the occasional small luminae; f, g) Fragments of narrow elongate anthers with same kind of pollen as in (i); h) Inner surface of anther wall showing small spherical orbicules;
Text-fig. 28. Scanning electron microscope (SEM) images of monocolpate pollen of Goczania inaequalis sp. nov.; Torres Vedras locality, Portugal. a) Holotype; stamen fragment that yielded the pollen in (b–f, k); b) Group of pollen grains showing distal and proximal surfaces and inner surface of anther wall with densely spaced orbicules; c) Inner surface of anther wall showing small, spherical orbicules with microechinate sculpturing; d, e, j–l) Pollen grains in distal and equatorial view (k) showing the long colpus with an irregular margin flanked by narrow bands of poorly differentiated microechinate; note that colpus is aligned perpendicular to the longest axes in elliptical grains and that the pollen wall is almost psilate around the equator and in the distal in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 28. Scanning electron microscope (SEM) images of monocolpate pollen of Goczania inaequalis sp. nov.; Torres Vedras locality, Portugal. a) Holotype; stamen fragment that yielded the pollen in (b–f, k); b) Group of pollen grains showing distal and proximal surfaces and inner surface of anther wall with densely spaced orbicules; c) Inner surface of anther wall showing small, spherical orbicules with microechinate sculpturing; d, e, j–l) Pollen grains in distal and equatorial view (k) showing the long colpus with an irregular margin flanked by narrow bands of poorly differentiated microechinate; note that colpus is aligned perpendicular to the longest axes in elliptical grains and that the pollen wall is almost psilate around the equator and in the distal
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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
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