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. 2017 Aug 17;7:8571. doi: 10.1038/s41598-017-08936-5

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Histological reconstruction of the recorded regions and functional maps of MK1 and MK2. (a,b) 3-D reconstruction (dorsal view) of the left hemisphere of MK1 (a) and MK2 (b), with superimposed number and class of neurons recorded from each site. (a1,b1) 3-D reconstruction (rostro-lateral view) of the same hemispheres of MK1 (a1) and MK2 (b1). (a2–b2) Examples of coronal sections at high magnification (photomicrograph of Nissl-stained section), showing where electrode tracks were identified. Dashed black lines in (a,b) and dashed black boxes in (a1–b1), labeled “c” and “d” indicate the position from which each coronal section was taken. SA, superior arcuate sulcus; IA, inferior arcuate sulcus; P, principalis sulcus; VPFC, ventral prefrontal cortex; OFC, orbitofrontal cortex.