The precise annotation and accurate identification of neural structures are prerequisites for studying mammalian brain function. The orientation of neurons and neural circuits is usually determined by mapping brain images to coarse axial-sampling planar reference atlases. However, individual differences at the cellular level likely lead to position errors and an inability to orient neural projections at single-cell resolution. Here, we present a high-throughput precision imaging method that can acquire a co-localized brain-wide data set of both fluorescent-labelled neurons and counterstained cell bodies at a voxel size of 0.32 × 0.32 × 2.0 μm in 3 days for a single mouse brain. We acquire mouse whole-brain imaging data sets of multiple types of neurons and projections with anatomical annotation at single-neuron resolution. The results show that the simultaneous acquisition of labelled neural structures and cytoarchitecture reference in the same brain greatly facilitates precise tracing of long-range projections and accurate locating of nuclei.

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By measuring the temperature-dependent tunneling spectroscopy of a set of flat-top Pb islands from 3.2 to 15 K, the limiting size of a nine-monolayer-thick Pb island with superconductivity above 3.2 K was determined to be ∼ 30 nm(2), in good agreement with the Anderson criterion. Further analysis indicates that the zero-temperature energy gap decreases significantly faster than the transition temperature when the Pb island size approaches this limit. This leads to a decrease of 2Δ(0)/k(B)T(C) from 4.5 to 3.3, thus showing that the Pb island superconductors undergo a change from strong to weak electron-phonon coupling.

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