Mammalian brain development and our grandmothering life history
Among mammals, including humans, adult brain size and the relative size of brain components depend precisely on the duration of a highly regular process of neural development. Much wider variation is seen in rates of body growth and the state of neural maturation at life history events like birth an...
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Veröffentlicht in: | Physiology & behavior 2018-09, Vol.193 (Pt A), p.55-68 |
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description | Among mammals, including humans, adult brain size and the relative size of brain components depend precisely on the duration of a highly regular process of neural development. Much wider variation is seen in rates of body growth and the state of neural maturation at life history events like birth and weaning. Large brains result from slow maturation, which in humans is accompanied by weaning early with respect to both neural maturation and longevity. The grandmother hypothesis proposes this distinctive combination of life history features evolved as ancestral populations began to depend on foods that just weaned juveniles couldn't handle. Here we trace possible reciprocal connections between brain development and life history, highlighting the resulting extended neural plasticity in a wider cognitive ecology of allomaternal care that distinguishes human ontogeny with consequences for other peculiarities of our lineage.
•Order and rate of neural maturation are stable in eutherian mammals, including humans.•Developmental duration, brain size, and longevity are all closely correlated.•But human infants are weaned notably early with respect to neural development.•The grandmother hypotheses links the evolution of human longevity to earlier weaning.•Grandmothering puts infants into unique social ecology at early neural development. |
doi_str_mv | 10.1016/j.physbeh.2018.01.013 |
format | Article |
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•Order and rate of neural maturation are stable in eutherian mammals, including humans.•Developmental duration, brain size, and longevity are all closely correlated.•But human infants are weaned notably early with respect to neural development.•The grandmother hypotheses links the evolution of human longevity to earlier weaning.•Grandmothering puts infants into unique social ecology at early neural development.</description><identifier>ISSN: 0031-9384</identifier><identifier>EISSN: 1873-507X</identifier><identifier>DOI: 10.1016/j.physbeh.2018.01.013</identifier><identifier>PMID: 29730032</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Allometries ; Animals ; Biological Evolution ; Brain - growth & development ; Brain growth ; Evo-devo ; Human evolution ; Humans ; Mammals - growth & development ; Maternal Behavior ; Neuromaturation ; Primate brain evolution</subject><ispartof>Physiology & behavior, 2018-09, Vol.193 (Pt A), p.55-68</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-48726bd9efc5caa8c6961cf222a22a8185f391804b0f42de6a075b2de03539073</citedby><cites>FETCH-LOGICAL-c365t-48726bd9efc5caa8c6961cf222a22a8185f391804b0f42de6a075b2de03539073</cites><orcidid>0000-0002-0558-4856</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.physbeh.2018.01.013$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29730032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hawkes, Kristen</creatorcontrib><creatorcontrib>Finlay, Barbara L.</creatorcontrib><title>Mammalian brain development and our grandmothering life history</title><title>Physiology & behavior</title><addtitle>Physiol Behav</addtitle><description>Among mammals, including humans, adult brain size and the relative size of brain components depend precisely on the duration of a highly regular process of neural development. Much wider variation is seen in rates of body growth and the state of neural maturation at life history events like birth and weaning. Large brains result from slow maturation, which in humans is accompanied by weaning early with respect to both neural maturation and longevity. The grandmother hypothesis proposes this distinctive combination of life history features evolved as ancestral populations began to depend on foods that just weaned juveniles couldn't handle. Here we trace possible reciprocal connections between brain development and life history, highlighting the resulting extended neural plasticity in a wider cognitive ecology of allomaternal care that distinguishes human ontogeny with consequences for other peculiarities of our lineage.
•Order and rate of neural maturation are stable in eutherian mammals, including humans.•Developmental duration, brain size, and longevity are all closely correlated.•But human infants are weaned notably early with respect to neural development.•The grandmother hypotheses links the evolution of human longevity to earlier weaning.•Grandmothering puts infants into unique social ecology at early neural development.</description><subject>Allometries</subject><subject>Animals</subject><subject>Biological Evolution</subject><subject>Brain - growth & development</subject><subject>Brain growth</subject><subject>Evo-devo</subject><subject>Human evolution</subject><subject>Humans</subject><subject>Mammals - growth & development</subject><subject>Maternal Behavior</subject><subject>Neuromaturation</subject><subject>Primate brain evolution</subject><issn>0031-9384</issn><issn>1873-507X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EoqXwCaAs2ST4kYe9qhDiJRWxAYmd5TiTxlUSBzup1L_HVQtbRleauzgzo7kIXROcEEzyu00yNDtfQpNQTHiCSRA7QXPCCxZnuPg6RXOMGYkF4-kMXXi_waFYys7RjIqCBU_naPmmuk61RvVR6ZTpowq20Nqhg36MVF9FdnLR2gXX2bEBZ_p11Joaosb40brdJTqrVevh6tgX6PPp8ePhJV69P78-3K9izfJsjFNe0LysBNQ600pxnYuc6JpSqoI44VnNBOE4LXGd0gpyhYusDAazjAlcsAW6PewdnP2ewI-yM15D26oe7OQlDWCBRSr2aHZAtbPeO6jl4Eyn3E4SLPfZyY08Zif32UlMgliYuzmemMoOqr-p37ACsDwAEB7dGnDSawO9hso40KOsrPnnxA9BqIJX</recordid><startdate>20180901</startdate><enddate>20180901</enddate><creator>Hawkes, Kristen</creator><creator>Finlay, Barbara L.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0558-4856</orcidid></search><sort><creationdate>20180901</creationdate><title>Mammalian brain development and our grandmothering life history</title><author>Hawkes, Kristen ; Finlay, Barbara L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-48726bd9efc5caa8c6961cf222a22a8185f391804b0f42de6a075b2de03539073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Allometries</topic><topic>Animals</topic><topic>Biological Evolution</topic><topic>Brain - growth & development</topic><topic>Brain growth</topic><topic>Evo-devo</topic><topic>Human evolution</topic><topic>Humans</topic><topic>Mammals - growth & development</topic><topic>Maternal Behavior</topic><topic>Neuromaturation</topic><topic>Primate brain evolution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hawkes, Kristen</creatorcontrib><creatorcontrib>Finlay, Barbara L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Physiology & behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hawkes, Kristen</au><au>Finlay, Barbara L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mammalian brain development and our grandmothering life history</atitle><jtitle>Physiology & behavior</jtitle><addtitle>Physiol Behav</addtitle><date>2018-09-01</date><risdate>2018</risdate><volume>193</volume><issue>Pt A</issue><spage>55</spage><epage>68</epage><pages>55-68</pages><issn>0031-9384</issn><eissn>1873-507X</eissn><abstract>Among mammals, including humans, adult brain size and the relative size of brain components depend precisely on the duration of a highly regular process of neural development. Much wider variation is seen in rates of body growth and the state of neural maturation at life history events like birth and weaning. Large brains result from slow maturation, which in humans is accompanied by weaning early with respect to both neural maturation and longevity. The grandmother hypothesis proposes this distinctive combination of life history features evolved as ancestral populations began to depend on foods that just weaned juveniles couldn't handle. Here we trace possible reciprocal connections between brain development and life history, highlighting the resulting extended neural plasticity in a wider cognitive ecology of allomaternal care that distinguishes human ontogeny with consequences for other peculiarities of our lineage.
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subjects | Allometries Animals Biological Evolution Brain - growth & development Brain growth Evo-devo Human evolution Humans Mammals - growth & development Maternal Behavior Neuromaturation Primate brain evolution |
title | Mammalian brain development and our grandmothering life history |
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