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Journal articles on the topic 'Papio'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 March 2023

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1

Grainger, J., S. Dufau, M. Montant, J. C. Ziegler, and J. Fagot. "Orthographic Processing in Baboons (Papio papio)." Science 336, no. 6078 (April 12, 2012): 245–48. http://dx.doi.org/10.1126/science.1218152.

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2

Wada, Juhn A., and Hirohito Tsuchimochi. "Cingulate Kindling in Senegalese Baboons, Papio papio." Epilepsia 36, no. 11 (November 1995): 1142–51. http://dx.doi.org/10.1111/j.1528-1157.1995.tb00474.x.

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3

Neff, Ellen P. "Papio genomes." Lab Animal 48, no. 4 (March 20, 2019): 112. http://dx.doi.org/10.1038/s41684-019-0277-y.

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4

Bains, W. "Comment on "Orthographic Processing in Baboons (Papio papio)"." Science 337, no. 6099 (September 6, 2012): 1173. http://dx.doi.org/10.1126/science.1224508.

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5

Naquet, Robert, and Anne Valin. "Myoclonia in Papio papio: Are they all “Epileptic” ?" Neural Plasticity 7, no. 1-2 (2000): 43–48. http://dx.doi.org/10.1155/np.2000.43.

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6

Barbet, Isabelle, and Joël Fagot. "Processing of contour closure by baboons (Papio papio)." Journal of Experimental Psychology: Animal Behavior Processes 37, no. 4 (2011): 407–19. http://dx.doi.org/10.1037/a0025365.

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7

EBBERT, M. A., W. C. McGREW, and L. F. MARCHANT. "Differences between chimpanzee and baboon gastrointestinal parasite communities." Parasitology 142, no. 7 (March 3, 2015): 958–67. http://dx.doi.org/10.1017/s0031182015000104.

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SUMMARYCross-species infection among humans, chimpanzees (Pan troglodytes) and baboons (Papio spp.) is potentially a significant public health issue in Africa, and of concern in the conservation of P. troglodytes. However, to date, no statistical comparisons have been made between the prevalence, richness and composition of parasite communities in sympatric populations of baboons and P. troglodytes. We compared parasite communities in sympatric P. troglodytes and Papio papio living in a wilderness site, in the Republic of Senegal, West Africa. We asked whether, in the absence of humans, there are significant differences between these hosts in their interactions with gastrointestinal parasites. We tested whether host, location, or time of collection accounted for variation in prevalence, richness and community composition, and compared prevalence across six studies. We concluded that, despite being closely related, there are significant differences between these two hosts with respect to their parasite communities. At our study site, prevalence of Balantidium, Trichuris and Watsonius was higher in P. papio. Papio papio harboured more parasites per host, and we found evidence of a positive association between Trichuris and Balantidium in P. troglodytes but not P. papio.

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8

Deruelle, Christine, Isabelle Barbet, Delphine Dépy, and Joël Fagot. "Perception of Partly Occluded Figures by Baboons (Papio Papio)." Perception 29, no. 12 (December 2000): 1483–97. http://dx.doi.org/10.1068/p3071.

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9

Fagot, Joël, and Christine Deruelle. "Perception of pictorial eye gaze by baboons ( Papio papio)." Journal of Experimental Psychology: Animal Behavior Processes 28, no. 3 (2002): 298–308. http://dx.doi.org/10.1037/0097-7403.28.3.298.

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10

Medam, Tiphaine, and Joël Fagot. "Behavioral assessment of combinatorial semantics in baboons (Papio papio)." Behavioural Processes 123 (February 2016): 54–62. http://dx.doi.org/10.1016/j.beproc.2015.10.016.

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11

Barbet, Isabelle, and Joël Fagot. "Perception of the corridor illusion by baboons (Papio papio)." Behavioural Brain Research 132, no. 1 (April 2002): 111–15. http://dx.doi.org/10.1016/s0166-4328(01)00393-x.

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12

Walberg, Fred, and Ole P. Ottersen. "Demonstration of GABA immunoreactive cells in the inferior olive of baboons (Papio papio and Papio anubis)." Neuroscience Letters 101, no. 2 (June 1989): 149–55. http://dx.doi.org/10.1016/0304-3940(89)90522-3.

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13

Brailowsky, Sim�n. "Myoclonus inPapio papio." Movement Disorders 6, no. 2 (1991): 98–104. http://dx.doi.org/10.1002/mds.870060203.

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14

Goffe, A. S., and J. Fischer. "Meat sharing between male and female Guinea baboons (Papio papio)." Primate Biology 3, no. 1 (February 4, 2016): 1–8. http://dx.doi.org/10.5194/pb-3-1-2016.

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Abstract. Meat sharing in non-human primates has been linked to a variety of functions, including harassment reduction, mate provisioning and status enhancement. We present observational data regarding male prey capture and male–female meat sharing in wild Guinea baboons. Guinea baboons live in a multilevel society that comprises units of males with associated females and, sometimes, secondary males. Several males of different units maintain strong bonds, resulting in the formation of parties within gangs. Female–male relationships persist irrespective of female reproductive states, yet females may also switch between males at all stages of the reproductive cycle. Our data show that males capture and kill a variety of prey, including hares and antelope. Males shared meat passively only with females in their social and reproductive units. The occurrence of oestrus females in the gang did not influence whether or not sharing would occur in that males did not share with oestrus females unless an affiliative relationship already persisted, indicating that short-term currency exchanges of meat for sex are unlikely. We hypothesise that males may benefit from feeding tolerance by retaining females, while females may increase access to potentially nutritious and rare food sources. Alternatively, females may prefer males that are generally less aggressive and thus also more likely to share meat. Long-term data will be needed to ultimately distinguish between the two accounts. Although there is no evidence that males intentionally provide necessary resources to particular females during times of high energetic demands and decreased foraging efficiency, as has been found in humans, and meat sharing is generally rare, it may have subtle, yet important effects on the maintenance of bonds in Guinea baboons.

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15

Grainger, J., S. Dufau, M. Montant, J. C. Ziegler, and J. Fagot. "Response to Comment on "Orthographic Processing in Baboons (Papio papio)"." Science 337, no. 6099 (September 6, 2012): 1173. http://dx.doi.org/10.1126/science.1224939.

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16

Fagot, Joël, and Carole Parron. "Relational matching in baboons (Papio papio) with reduced grouping requirements." Journal of Experimental Psychology: Animal Behavior Processes 36, no. 2 (2010): 184–93. http://dx.doi.org/10.1037/a0017169.

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17

Saëz, H. "Levures de la cavité buccale du Babouin, Papio papio (Desm.)." Zentralblatt für Veterinärmedizin Reihe B 17, no. 3 (May 13, 2010): 381–88. http://dx.doi.org/10.1111/j.1439-0450.1970.tb01450.x.

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18

Malassis, Raphaëlle, Gilles Gheusi, and Joël Fagot. "Assessment of metacognitive monitoring and control in baboons (Papio papio)." Animal Cognition 18, no. 6 (August 2, 2015): 1347–62. http://dx.doi.org/10.1007/s10071-015-0907-8.

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19

Medam, Tiphaine, Yousri Marzouki, Marie Montant, and Joël Fagot. "Categorization does not promote symmetry in Guinea baboons (Papio papio)." Animal Cognition 19, no. 5 (June 8, 2016): 987–98. http://dx.doi.org/10.1007/s10071-016-1003-4.

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20

Naquet, R., C. Silva-Barrat, and C. Menini. "Reflex epilepsy in the Papio-papio baboon, particularly photosensitive epilepsy." Italian Journal of Neurological Sciences 16, no. 1-2 (March 1995): 119–25. http://dx.doi.org/10.1007/bf02229084.

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21

Rivero, Julia, Rocío Callejón, and Cristina Cutillas. "Complete Mitochondrial Genome of Trichuristrichiura from Macaca sylvanus and Papio papio." Life 11, no. 2 (February 6, 2021): 126. http://dx.doi.org/10.3390/life11020126.

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Trichuriasis is among the most prevalent worldwide parasitism caused by helminths. For many years, Trichuris spp. have been described with a relatively narrow range of both morphological and biometrical features. The use of the complete mitochondrial genome (mitogenome) is an alternative and powerful molecular method for inferring phylogenies. Here, we present an overview of the contributions of mitogenome for Trichuris spp. from human and non-human primates. In addition, we carry out structural and phylogenetic comparative analyses with genomes of Trichuris species available in public datasets. The complete mt genomes of Trichuris trichiura and Trichuris sp. from Macaca sylvanus and T. trichiura from Papio papio are 14,091 bp, 14,047 bp and 14,089 bp in length, respectively. The three mt genomes are circular and consist of 37 genes—13 PCGs (cox1–3, nad1–6, nad4L, atp6, atp8 and cob), 22 transfer RNA genes (tRNAs), and two rRNAs (rrnL and rrnS). The molecular evidence presented here supports the hypothesis that T. trichiura de M. sylvanus (TMF31) and T. trichiura de P. papio (TPM1) were similar but genetically different with respect to Trichuris sp. from macaques (TMM5). The phylogenetic study also supported the evolution of the different Trichuris species. In conclusion, we suggest the existence of two cryptic species parasitizing M. sylvanus.

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22

Nda, Kacou, Laiban Dahourou, Papa Ndiaye, Stacy Lindshield, Oubri GBATI, and Amadou Traore. "Gastrointestinal parasites of baboons (Papio papio) in NiokoloKoba National Park, Senegal." Open Veterinary Journal 12, no. 4 (2022): 481. http://dx.doi.org/10.5455/ovj.2022.v12.i4.9.

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Abstract Background: Primates can harbour parasites that could be pathogenic or not for humans and primates themselves. It is necessary to know the parasitological situation of the primates that are under surveillance in the park. Aim: The purpose of this study was to estimate the prevalence and diversity of gastrointestinal parasites, including zoonotic potential parasites, in baboons in the Niokolo-Koba National Park located in Senegal. Method: Faecal samples (n=50) from two groups of Baboons (A and B) were collected in October 2019. Faecal samples were processed using the flotation technique and the modified Ritchie method. Slides were examined microscopically, and the parasite identification was based on morphology, colour, and parasite content. Results: A total of seven nematodes (Strongyloides sp., Trichirus sp., Ancylostoma sp., Mammo monogamus, Enterobius sp., Strongyloides stercoralis, Strongle digestif), one cestode (Bertiella sp.) and one trematode (Fasciolopsis sp.) were identified. The overall prevalence was 78% while poly-infestation prevalence was 49%. The parasite with zoonotic potential, Strongyloides stercoralis, was identified in group B samples. Trichuris sp. which is common and pathogenic to humans and primates was present with a prevalence of 52% and of 32% in groups A and B, respectively. Conclusion: These results suggest that baboons are infested with zoonotic parasites and this situation could expose people working in this park to infection. Contact between humans and these baboons or their faeces could expose to infection with zoonotic parasites.

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23

Parron, Carole, Christine Deruelle, and Joël Fagot. "Processing of biological motion point-light displays by baboons (Papio papio)." Journal of Experimental Psychology: Animal Behavior Processes 33, no. 4 (2007): 381–91. http://dx.doi.org/10.1037/0097-7403.33.4.381.

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24

Dépy, Delphine, Joël Fagot, and Jacques Vauclair. "Processing of above/below categorical spatial relations by baboons (Papio papio)." Behavioural Processes 48, no. 1-2 (November 1999): 1–9. http://dx.doi.org/10.1016/s0376-6357(99)00055-8.

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25

Wasserman, Edward A., Joël Fagot, and Michael E. Young. "Same–different conceptualization by baboons (Papio papio): The role of entropy." Journal of Comparative Psychology 115, no. 1 (2001): 42–52. http://dx.doi.org/10.1037/0735-7036.115.1.42.

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26

Emperaire-Le Pouleuf, N., and A. Ottomani. "Neurotoxicité et cardiotoxicité de la bupivacaïne chez le babouin papio papio." Annales Françaises d'Anesthésie et de Réanimation 6, no. 5 (January 1987): 467. http://dx.doi.org/10.1016/s0750-7658(87)80377-5.

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27

Fagot, Joël, Isabelle Barbet, Carole Parron, and Christine Deruelle. "Amodal completion by baboons (Papio papio): contribution of background depth cues." Primates 47, no. 2 (January 28, 2006): 145–50. http://dx.doi.org/10.1007/s10329-005-0165-5.

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28

Ménini, C., C. Silva-Barrat, P. Bryère, I. Rektor, and R. Naquet. "Comparison of two types of myoclonus in the baboon papio papio." Electroencephalography and Clinical Neurophysiology 61, no. 3 (September 1985): S56. http://dx.doi.org/10.1016/0013-4694(85)90240-8.

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29

Lacreuse, Agnès, Julie Gullstrand, and Joël Fagot. "Sex differences in inhibitory control in socially-housed baboons (Papio papio)." Behavioural Brain Research 312 (October 2016): 231–37. http://dx.doi.org/10.1016/j.bbr.2016.06.032.

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30

Reboul, Anne, Olivier Mascaro, Nicolas Claidière, and Joël Fagot. "Are monkeys sensitive to informativeness: An experimental study with baboons (Papio papio)." PLOS ONE 17, no. 7 (July 5, 2022): e0270502. http://dx.doi.org/10.1371/journal.pone.0270502.

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Informativeness (defined as reduction of uncertainty) is central in human communication. In the present study, we investigate baboons’ sensitivity to informativeness by manipulating the informativity of a cue relative to a response display and by allowing participants to anticipate their answers or to wait for a revealed answer (with variable delays). Our hypotheses were that anticipations would increase with informativity, while response times to revealed trials would decrease with informativity. These predictions were verified in Experiment 1. In Experiments 2 and 3, we manipulated rewards (rewarding anticipation responses at 70% only) to see whether reward tracking alone could account for the results in Experiment 1. We observed that the link between anticipations and informativeness disappeared, but not the link between informativeness and decreased RTs for revealed trials. Additionally, in all three experiments, the number of correct answers in revealed trials with fast reaction times (< 250ms) increased with informativeness. We conclude that baboons are sensitive to informativeness as an ecologically sound means to tracking reward.

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31

Bonté, Elodie, Timothy Flemming, and Joël Fagot. "Executive control of perceptual features and abstract relations by baboons (Papio papio)." Behavioural Brain Research 222, no. 1 (September 2011): 176–82. http://dx.doi.org/10.1016/j.bbr.2011.03.034.

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32

D'Hooghe, T. M., C. S. Bambra, I. De Jonge, J. M. Lauweryns, B. M. Raeymaekers, and P. R. Koninckx. "The effect of pregnancy on endometriosis in baboons (Papio anubis, Papio cynocephalus) *." Archives of Gynecology and Obstetrics 261, no. 1 (December 10, 1997): 15–19. http://dx.doi.org/10.1007/s004040050191.

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33

Howlett, Caroline, Andrew R. Marshall, and William O. H. Hughes. "Digit Ratios and Dominance in Female Baboons (Papio hamadryas and Papio ursinus)." International Journal of Primatology 33, no. 6 (September 1, 2012): 1439–52. http://dx.doi.org/10.1007/s10764-012-9636-x.

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34

Roberts, Trina E., Tim R. B. Davenport, Kyndall B. P. Hildebrandt, Trevor Jones, William T. Stanley, Eric J. Sargis, and Link E. Olson. "The biogeography of introgression in the critically endangered African monkey Rungwecebus kipunji." Biology Letters 6, no. 2 (November 11, 2009): 233–37. http://dx.doi.org/10.1098/rsbl.2009.0741.

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In the four years since its original description, the taxonomy of the kipunji ( Rungwecebus kipunji ), a geographically restricted and critically endangered African monkey, has been the subject of much debate, and recent research suggesting that the first voucher specimen of Rungwecebus has baboon mitochondrial DNA has intensified the controversy. We show that Rungwecebus from a second region of Tanzania has a distinct mitochondrial haplotype that is basal to a clade containing all Papio species and the original Rungwecebus voucher, supporting the placement of Rungwecebus as the sister taxon of Papio and its status as a separate genus. We suggest that the Rungwecebus population in the Southern Highlands has experienced geographically localized mitochondrial DNA introgression from Papio , while the Ndundulu population retains the true Rungwecebus mitochondrial genome.

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35

Zinner, Dietmar, Matthias Klapproth, Andrea Schell, Lisa Ohrndorf, Desalegn Chala, Jörg U. Ganzhorn, and Julia Fischer. "Comparative ecology of Guinea baboons (<i>Papio papio</i>)." Primate Biology 8, no. 1 (May 21, 2021): 19–35. http://dx.doi.org/10.5194/pb-8-19-2021.

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Abstract. Thorough knowledge of the ecology of a species or population is an essential prerequisite for understanding the impact of ecology on the evolution of their respective social systems. Because of their diversity of social organizations, baboons (Papio spp.) are a useful model for comparative studies. Comparative ecological information was missing for Guinea baboons (Papio papio), however. Here we provide data on the ecology of Guinea baboons in a comparative analysis on two geographical scales. First, we compare climate variables and land cover among areas of occurrence of all six baboon species. Second, we describe home range size, habitat use, ranging behaviour, and diet from a local population of Guinea baboons ranging near the Centre de Recherche de Primatologie (CRP) Simenti in the Niokolo-Koba National Park, Senegal. Home ranges and daily travel distances at Simenti varied seasonally, yet the seasonal patterns in their daily travel distance did not follow a simple dry vs. rainy season pattern. Chemical food composition falls within the range of other baboon species. Compared to other baboon species, areas occupied by Guinea baboons experience the highest variation in precipitation and the highest seasonality in precipitation. Although the Guinea baboons' multi-level social organization is superficially similar to that of hamadryas baboons (P. hamadryas), the ecologies of the two species differ markedly. Most Guinea baboon populations, including the one at Simenti, live in more productive habitats than hamadryas baboons. This difference in the ecology of the two species contradicts a simple evolutionary relation between ecology and social system and suggests that other factors have played an additional role here.

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36

Wallez, Catherine, and Jacques Vauclair. "Human (Homo sapiens) and baboon (Papio papio) chimeric face processing: Right-hemisphere involvement." Journal of Comparative Psychology 127, no. 3 (August 2013): 237–44. http://dx.doi.org/10.1037/a0031494.

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37

Vokey, John R., and Randall K. Jamieson. "A Visual-Familiarity Account of Evidence for Orthographic Processing in Baboons (Papio papio)." Psychological Science 25, no. 4 (February 6, 2014): 991–96. http://dx.doi.org/10.1177/0956797613516634.

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38

Goujon, Annabelle, and Joel Fagot. "Learning of spatial statistics in nonhuman primates: Contextual cueing in baboons (Papio papio)." Behavioural Brain Research 247 (June 2013): 101–9. http://dx.doi.org/10.1016/j.bbr.2013.03.004.

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39

Martin-Malivel, Julie. "Discrimination of contour-deleted images in baboons (Papio papio) and chimpanzees (Pan troglodytes)." Animal Cognition 14, no. 3 (January 12, 2011): 415–26. http://dx.doi.org/10.1007/s10071-010-0376-z.

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40

Pope, Sarah M., Adrien Meguerditchian, William D. Hopkins, and Joël Fagot. "Baboons (Papio papio), but not humans, break cognitive set in a visuomotor task." Animal Cognition 18, no. 6 (July 21, 2015): 1339–46. http://dx.doi.org/10.1007/s10071-015-0904-y.

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41

Satoh, K., and H. C. Fibiger. "Distribution of central cholinergic neurons in the baboon (papio papio). I. General morphology." Journal of Comparative Neurology 236, no. 2 (June 8, 1985): 197–214. http://dx.doi.org/10.1002/cne.902360205.

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42

Ferretti, Carlo, Jakobus Hoffman, and Ugo Ripamonti. "The Induction of Bone Formation by the recombinant human transforming growth Factor-β3 : From preclinical studies in Papio ursinus to translational research in Homo sapiens." South African Dental Journal 77, no. 03 (April 30, 2022): 121–34. http://dx.doi.org/10.17159/2519-0105/2022/v77no3a1.

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Skeletal bone defects of the axial or the craniomaxillofacial skeletons still present formidable challenges to skeletal reconstructionists, tissue biologists and modern medicine. In systematic research experiments in the Chacma baboon Papio ursinus our laboratories have shown the previously unreported osteoinductive activity of the three mammalian transforming growth factor-β (TGF-β) isoforms. This review discusses the induction of bone formation by the mammalian TGF-βs with particular reference to the substantial and rapid induction of bone by the recombinant hTGF-β3 from the laboratory benches, to pre-clinical studies in heterotopic and orthotopic mandibular sites of Papio ursinus to clinical translation in human patients. Design and MethodsA series of systematic research experiments in Papio ursinus using the hTGF-β3 together with earlier experiments using the -β1 and β2 isoforms are reviewed and re-analyzed molecularly nd morphologically to provide the basic research data for the reported clinical translation in human patients. Results The three mammalian hTGF-β isoforms and notably hTGF-β3 induce rapid and substantial induction of heterotopic bone in intramuscular sites of Papio ursinus. Relatively low doses of hTGF-β1or hTGF-β3 in binary application with hBMP-7 synergize to induce massive corticalized ossicles in the rectus abdominis muscle. In orthotopic mandibular sites, 125 and250 µg doses of hTGF-β3 induce bone formation across large mandibular defects in Papio ursinus with corticalized buccal and lingual plates by day 30, with modeling and maintenance of corticalized bone by 9 to 12 months after implantation of the 250 µg dose in 3 cm mandibular defects Papio ursinus. Discussion hTGF-β3 significantly up-regulates RUNX-2 and Osteocalcin expression on day 15 controlling the differentiation of progenitor stem cells into the osteoblastic lineage. The induction of bone by the hTGF-β3 is via the bone morphogenetic proteins pathway; hTGF-β3 controls theinduction of bone by regulating the expression of BMPs gene and gene products via Noggin expression, eliciting bone induction by up-regulating exogenous BMPs.

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43

Fagot, Joël, and Jacques Vauclair. "Video-task assessment of stimulus novelty effects on hemispheric lateralization in baboons (Papio papio)." Journal of Comparative Psychology 108, no. 2 (1994): 156–63. http://dx.doi.org/10.1037/0735-7036.108.2.156.

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44

Vauclair, Jacques, and Joël Fagot. "Manual and hemispheric specialization in the manipulation of a joystick by baboons (Papio papio)." Behavioral Neuroscience 107, no. 1 (1993): 210–14. http://dx.doi.org/10.1037/0735-7044.107.1.210.

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45

El Kharroussi, M., D. Françon, W. Ben Jelloun, and M. Hugon. "Potentiels évoqués somesthésiques: morphologie et relations interaréales SI-MI chez le singe (Papio papio)." Neurophysiologie Clinique/Clinical Neurophysiology 26, no. 5 (January 1996): 279–99. http://dx.doi.org/10.1016/s0987-7053(97)85096-4.

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46

D'Hooghe, Thomas M., Charanjit S. Bambra, Barbara M. Raeymaekers, Inge De Jonge, Jo M. Lauweryns, and P. R. Koninckx. "Intrapelvic injection of menstrual endometrium causes endometriosis in baboons (Papio cynocephalus and Papio anubis)." American Journal of Obstetrics and Gynecology 173, no. 1 (July 1995): 125–34. http://dx.doi.org/10.1016/0002-9378(95)90180-9.

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47

Dépy, Delphine, Joel Fagot, and Jacques Vauclair. "Comparative Assessment of Distance Processing and Hemispheric Specialization in Humans and Baboons (Papio papio)." Brain and Cognition 38, no. 2 (November 1998): 165–82. http://dx.doi.org/10.1006/brcg.1998.1027.

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48

Samson, David R., and Robert W. Shumaker. "Orangutans (Pongo spp.) have deeper, more efficient sleep than baboons (Papio papio) in captivity." American Journal of Physical Anthropology 157, no. 3 (March 7, 2015): 421–27. http://dx.doi.org/10.1002/ajpa.22733.

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49

Lepoivre, Hugues, and Berthille Pallaud. "Social facilitation in a troop of Guinea Baboons (Papio papio) living in an enclosure." Behavioural Processes 11, no. 4 (November 1985): 405–18. http://dx.doi.org/10.1016/0376-6357(85)90005-1.

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50

Gauthier, Claude-Anne. "Reproductive parameters and paracallosal skin color changes in captive female Guinea baboons,Papio papio." American Journal of Primatology 47, no. 1 (1999): 67–74. http://dx.doi.org/10.1002/(sici)1098-2345(1999)47:1<67::aid-ajp8>3.0.co;2-#.

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