000910717 001__ 910717
000910717 005__ 20221116131014.0
000910717 0247_ $$2WOS$$aWOS:000772245500002
000910717 037__ $$aFZJ-2022-04087
000910717 1001_ $$0P:(DE-HGF)0$$aAbdullah, I.$$b0
000910717 1112_ $$a91st Annual Meeting of the American Associatin of Biological Anthropologists$$cDenver$$d2022-03-23 - 2022-04-01$$wUSA
000910717 245__ $$aComparison of Temporal Cortex Cytoarchitectural Variability Across Primates
000910717 260__ $$c2022
000910717 3367_ $$0PUB:(DE-HGF)1$$2PUB:(DE-HGF)$$aAbstract$$babstract$$mabstract$$s1668589466_11092
000910717 3367_ $$033$$2EndNote$$aConference Paper
000910717 3367_ $$2BibTeX$$aINPROCEEDINGS
000910717 3367_ $$2DRIVER$$aconferenceObject
000910717 3367_ $$2DataCite$$aOutput Types/Conference Abstract
000910717 3367_ $$2ORCID$$aOTHER
000910717 520__ $$aPrimates with larger brains tend to possess a greater number of distinct cortical areas, but there are limited data from systematic quantita-tive analysis of cytoarchitectural variation across the cortex of different species. The current study aimed to determine if brain size covaries with cellular distributions across the cortical surface. Greater cytoarchitectural differentiation might indicate increased modularity of cortical func-tion. Our preliminary sample included coronal histological sections of the temporal lobe from Indri indri, Lagothrix lagotricha, Saguinus midas, and Saimiri sciureus. The temporal lobe contains cortical areas that function in higher-order audi-tory processing and visual object recognition. The cortex was sampled from c200 equidis-tantly-located sites in each brain from sections representing the entire rostrocaudal axis of the temporal lobe. From each site, characteristics of cellular distributions were quantiܪed using image analysis procedures to obtain data on vertical changes from the top of layer II to bottom of layer VI in: 1) the proportion of cell proܪles versus neuropil space (grey level) and 2) the size distri-bution and density of cell proܪles. Results showed that the coefܪcient of variation in cortical grey level increased with brain size (rho"0.95, P"0.05). Variation in cell proܪle sizes tended to decrease, but not signiܪcantly (rho"-0.80, P"0.20). We found no consistent rostrocaudal gradient of variation in these aspects of cytoarchitecture across temporal lobe sections in the sample. Further analyses will incorporate a greater range of primates. These studies will contribute to our understanding of developmental mechanisms in shaping primate cortical structure.Same-sex sexual behavior in wild woolly monkeys (Lagothrix lagotricha poeppigii)LAURA A. ABONDANO1, KELSEY M. ELLIS2 and ANTHONY DI FIORE1,31Department of Anthropology, University of Texas at Austin, 2Department of Anthropology, Miami University, 3Tiputini Biodiversity Station, College of Biological and Environmental Sciences, Universidad San Francisco de QuitoStudies of sexual behaviors and reproductive strat-egies have often focused on interactions between different-sex dyads, potentially underestimating the frequency of same-sex sexual behavior (SSSB) among animal species. However, SSSB is ubiquitous across the animal kingdom, and, among primates, there are a variety of species that commonly display SSSB (e.g., bonobos, macaques, capuchins). Here, we present novel data on same-sex mounting behavior, one type of SSSB, in wild woolly monkeys (Lagothrix lagotricha poeppigii) living in a pristine tropical rainforest in the Ecuadorian Amazon. Between 2014 and 2018, we recorded data on sexual behaviors among adult and subadult individuals in four neighboring social groups. Of 279 observed cases of mounting, ܪve (1.8%) were among same-sex dyads (four female-female and one male-male). Interestingly, all ܪve cases involved at least one subadult individual, suggesting that in woolly monkeys SSSB may be used as an exper-imental or learning strategy for subadults prior to reaching sexual maturity as adults. However, further investigations are needed to better under-stand the function of SSSB in woolly monkeys. With this study, we hope to grow the compara-tive data set to better understand the function of non-conceptive sexual behaviors, including SSSB, among animals including primates.
000910717 536__ $$0G:(DE-HGF)POF4-5251$$a5251 - Multilevel Brain Organization and Variability (POF4-525)$$cPOF4-525$$fPOF IV$$x0
000910717 588__ $$aDataset connected to Web of Science, Web of Science, , Journals: juser.fz-juelich.dejuser.fz-juelich.de
000910717 7001_ $$0P:(DE-HGF)0$$aDecasien, A.$$b1
000910717 7001_ $$0P:(DE-HGF)0$$aTaylor, C.$$b2
000910717 7001_ $$0P:(DE-HGF)0$$aMcniff, G.$$b3
000910717 7001_ $$0P:(DE-HGF)0$$aLongtin, A.$$b4
000910717 7001_ $$0P:(DE-HGF)0$$aBarone, C.$$b5
000910717 7001_ $$0P:(DE-HGF)0$$aSnyder, A$$b6
000910717 7001_ $$0P:(DE-HGF)0$$aLoganathan, A.$$b7
000910717 7001_ $$0P:(DE-HGF)0$$aWahed, Z.$$b8
000910717 7001_ $$0P:(DE-HGF)0$$aPipa, Z.$$b9
000910717 7001_ $$0P:(DE-Juel1)191360$$aHerold, Christina$$b10$$ufzj
000910717 7001_ $$0P:(DE-Juel1)131631$$aAmunts, Katrin$$b11$$ufzj
000910717 7001_ $$0P:(DE-HGF)0$$aSherwood, C.$$b12
000910717 909CO $$ooai:juser.fz-juelich.de:910717$$pVDB
000910717 9101_ $$0I:(DE-588b)5008462-8$$6P:(DE-Juel1)191360$$aForschungszentrum Jülich$$b10$$kFZJ
000910717 9101_ $$0I:(DE-588b)5008462-8$$6P:(DE-Juel1)131631$$aForschungszentrum Jülich$$b11$$kFZJ
000910717 9131_ $$0G:(DE-HGF)POF4-525$$1G:(DE-HGF)POF4-520$$2G:(DE-HGF)POF4-500$$3G:(DE-HGF)POF4$$4G:(DE-HGF)POF$$9G:(DE-HGF)POF4-5251$$aDE-HGF$$bKey Technologies$$lNatural, Artificial and Cognitive Information Processing$$vDecoding Brain Organization and Dysfunction$$x0
000910717 9141_ $$y2022
000910717 9201_ $$0I:(DE-Juel1)INM-1-20090406$$kINM-1$$lStrukturelle und funktionelle Organisation des Gehirns$$x0
000910717 980__ $$aabstract
000910717 980__ $$aVDB
000910717 980__ $$aI:(DE-Juel1)INM-1-20090406
000910717 980__ $$aUNRESTRICTED