This is a population average over 1,065 young adults. Individual
anatomy varies. Tractography can invent connections and miss real ones
(Yeh 2022). These are not axons. A millimetre total under an action is
the sum of each bundle's own median streamline path length, not one
anatomical path. Path length is not the Euclidean span of the named
structure (the anterior commissure is the extreme case).
What this atlas file does not contain. The
ingested release hcp1065_avg_tracts_trk.zip (SHA-256
344aad43…779c67) has 87 named .trk.gz files.
That HCP1065 zip has no spinothalamic tract, no forceps minor, no medial
forebrain bundle, no trigeminothalamic tract, and no mammillothalamic tract.
The corpus callosum is one file. Pain sketches therefore start at
thalamus or trigeminal root. Mood sketches use uncinate, cingulum,
anterior thalamic radiation, and fornix. Anterior thalamic radiation
is not the slMFB (Bracht 2015; Denier 2020).
Sensory versus affective pain. Superior
thalamic radiation is used here as a discriminative body-map stand-in.
The HCP1065 file also carries motor thalamocortical fibres (VL/VA to
M1), so the label is incomplete. Affective unpleasantness is sketched
with anterior thalamic radiation, cingulum, and uncinate. Face pain is
drawn crossed (left trigeminal file to right superior thalamic
radiation) because second-order trigeminal nociception decussates; the
crossing itself is not in the atlas.
Three MNI templates. Streamlines are Yeh 2022
ICBM 2009a. The glass cortex is HCP S1200 fs_LR, MNI152NLin6Asym. The
cerebellum remainder is MNI152NLin2009cAsym. The TrackVis affine maps
file millimetres to RAS millimetres. It does not convert one template
into another. Laterality checks cannot detect a several-millimetre
template offset.
Uncinate stems. HCP1065 ships a whole uncinate
per hemisphere. Bhatia 2018 found FA reductions in subgenual and polar
stems, not the lateral stem. This page cannot isolate those stems.
S1, S2, and limbic cortex. Those tints are
Glasser HCP-MMP1 parcels already on the surface, not new anatomy.
S1 is 3a, 3b, 1, and 2: a strip, not a homunculus. S2 is opercular
OP1, OP2-3, and OP4. Limbic cortex is named cingulate, orbital,
entorhinal, parahippocampal, and hippocampal surface parcels. It is
not one organ. Amygdala and accumbens are not on this cortical map.
Pain-map cortex. The default cortical tint is
Glasser MMP1 parcels grouped to match a teaching figure: S1, S2, M1,
SMA, TPJ, ACC, PFC, and insula. Those are parcel stand-ins, not
Brodmann drawings and not a homunculus.
Ghost nuclei. Thalamus, caudate, putamen,
accumbens, amygdala, hippocampus, and brainstem are HCP Atlas_ROIs
(Open Access Data Use Terms). PAG and locus coeruleus are Harvard AAN
atlas v2.0 (CC0). Rostral ventral medulla is not in either atlas and
is not drawn. Thalamus and accumbens mesh edits are specified on
/modeling, not applied here.
Cervical cord columns. The second scene is
AMU7T occupancy meshes (MIT) of Lévy/Hausman parcels in straightened
PAM50-space millimetres, shown as a filled C5 cross-section (extruded
2 mm). That disk is not a GPU clip of a hollow C1–C7 surface.
The spinal lemniscus parcel does not isolate the spinothalamic tract
and is not 7 T tractography. It is not an HCP1065 file. HCP1065 still
has no spinothalamic tract. Thoracic, lumbar, and brainstem / Sp5c are
labelled Book hatched schematics on the same picker (not PAM50, not
Navigator). The third canvas defaults to the Book cervical circuit
(Rexed/Todd). C5 anatomy remains a selectable Atlas view: AMU7T occupancy
of the cervical dorsal horn, with Lissauer as the licensed stand-in for
fine DRG afferents after they enter and Book DRG/rootlets (no licensed
DRG volume; PAM50_rootlets is not used). Cord sketches have no pulse:
occupancy meshes have no atlas median path length.
Data were provided in part by the Human Connectome Project, WU-Minn
Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil;
1U54MH091657) funded by the 16 NIH Institutes and Centers that support
the NIH Blueprint for Neuroscience Research; and by the McDonnell Center
for Systems Neuroscience at Washington University.