Evidence map›Paper›PMID 38991613›Full record

ArticleCurrent biology : CB2024

A prominent vertical occipital white matter fasciculus unique to primate brains.

Hiromasa Takemura, Takaaki Kaneko, Chet C Sherwood, G Allan Johnson, Markus Axer, Erin E Hecht, Frank Q Ye, David A Leopold

Abstract read
In one paragraph

Article in Current biology : CB, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hiromasa TakemuraDivision of Sensory and Cognitive Brain Mapping, Department of System Neuroscience, National Institute for Physiological Sciences, 38 Nishigonaka Myodaiji, Okazaki-shi, Aichi 444-8585, Japan; The Graduate Institute for Advanced Studies, SOKENDAI, Shonan Village, Hayama-cho, Kanagawa 240-0193, Japan; Center for Information and Neural Networks (CiNet), Advanced ICT Research Institute, National Institute of Information and Communications Technology, 1-4 Yamadaoka, Suita-shi, Osaka 565-0871, Japan. Electronic address: htakemur@nips.ac.jp.
Takaaki KanekoCenter for the Evolutionary Origins of Human Behavior, Kyoto University, 41-2 Kanrin, Inuyama-shi, Aichi 484-8506, Japan; Division of Behavioral Development, Department of System Neuroscience, National Institute for Physiological Sciences, 38 Nishigonaka Myodaiji, Okazaki-shi, Aichi, Japan.
Chet C SherwoodDepartment of Anthropology, The George Washington University, 800 22nd St. NW, Washington, DC 20052, USA.
G Allan JohnsonDepartment of Radiology, Duke Center for In Vivo Microscopy, Duke Medical Center, 311 Research Drive, Durham, NC 27710, USA; Department of Biomedical Engineering, Duke University, 101 Science Dive., Durham, NC 27705, USA.
Markus AxerInstitute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Jülich 52425, Germany; Department of Physics, School of Mathematics and Natural Sciences, University of Wuppertal, Gaußstraße 20 42119, Wuppertal, Germany.
Erin E HechtDepartment of Human Evolutionary Biology, Harvard University, 11 Divinity Avenue, Cambridge, MA 02138, USA.
Frank Q YeNeurophysiology Imaging Facility, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke, National Eye Institute, National Institutes of Health, Bethesda, MD 20814, USA.
David A LeopoldNeurophysiology Imaging Facility, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke, National Eye Institute, National Institutes of Health, Bethesda, MD 20814, USA; Systems Neurodevelopment Laboratory, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20814, USA. Electronic address: leopoldd@mail.nih.gov.

Funding

The Pathophysiology and Treatment Of Children With Severe Mood DysregulationZIAMH002786 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LEIBENLUFT, ELLEN · 2009 to 2023
$34.0M
Neurophysiology Imaging Facility Core: Functional and Structural MRIZICMH002899 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LEOPOLD, DAVID A · 2009 to 2025
$29.1M
Neurophysiology of Visual PerceptionZIAMH002838 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LEOPOLD, DAVID A · 2009 to 2025
$14.0M
The Neural Underpinnings of Functional MRI NetworksZIAMH002896 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LEOPOLD, DAVID A · 2009 to 2025
$13.6M
Intramural NIH HHS ZIA MH002786Intramural NIH HHS ZIA MH002896Intramural NIH HHS ZIC MH002899
6 · The paper itself

Abstract

Vision in humans and other primates enlists parallel processing streams in the dorsal and ventral visual cortex, known to support spatial and object processing, respectively. These streams are bridged, however, by a prominent white matter tract, the vertical occipital fasciculus (VOF), identified in both classical neuroanatomy and recent diffusion-weighted magnetic resonance imaging (dMRI) studies. Understanding the evolution of the VOF may shed light on its origin, function, and role in visually guided behaviors. To this end, we acquired high-resolution dMRI data from the brains of select mammalian species, including anthropoid and strepsirrhine primates, a tree shrew, rodents, and carnivores. In each species, we attempted to delineate the VOF after first locating the optic radiations in the occipital white matter. In all primate species examined, the optic radiation was flanked laterally by a prominent and coherent white matter fasciculus recognizable as the VOF. By contrast, the equivalent analysis applied to four non-primate species from the same superorder as primates (tree shrew, ground squirrel, paca, and rat) failed to reveal white matter tracts in the equivalent location. Clear evidence for a VOF was also absent in two larger carnivore species (ferret and fox). Although we cannot rule out the existence of minor or differently organized homologous fiber pathways in the non-primate species, the results suggest that the VOF has greatly expanded, or possibly emerged, in the primate lineage. This adaptation likely facilitated the evolution of unique visually guided behaviors in primates, with direct impacts on manual object manipulation, social interactions, and arboreal locomotion.

Indexed as

PrimatesVisual CortexWhite MatterAnimalsBiological EvolutionCarnivoraDiffusion Magnetic Resonance ImagingOccipital LobeRodentiaSpecies SpecificityVisual Pathwayscomparative studydiffusion MRIvertical occipital fasciculusvisual systemwhite matter

Identifiers

PMID38991613
PMCPMC11338705

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.