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0345256861
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note
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Preliminary descriptions of large hominoid specimens from Nachola (20, 23, 24) and differences in the morphology of hominoid humeri from Maboko (35) suggest that material herein assigned to Equatorius may comprise more than one species.
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20
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0003060163
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D. R. Begun, C. V. Ward, M. D. Rose, Eds. Plenum, New York
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Rose, M.D.1
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0000527920
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D. R. Begun, C. V. Ward, M. D. Rose, Eds. Plenum, New York
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C. V. Ward, in Function, Phylogeny, and Fossils, D. R. Begun, C. V. Ward, M. D. Rose, Eds. (Plenum, New York, 1997), pp. 101-130.
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Ward, C.V.1
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0032084643
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Shimizu, D.4
Ishida, H.5
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23
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0345256859
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note
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The entire type series of G. darwini from Devínska Nová Ves, Slovakia, consists of four isolated molar teeth, which limits comparisons with other taxa. However, the two lower molars in the series (including the type specimen) have prominent buccal cingulae, a primitive hominoid character that is rare in E. africanus (6).
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26
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0002807545
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H. Ishida, M. Pickford, H. Nakaya, Y. Nakano, ibid. 2, 73 (1984).
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27
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0344394014
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note
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McCrossin and Benefit (6) propose that new upper central incisors from Maboko extend the range of variation from the site to encompass the morphology of the Fort Ternan incisor. However, details of these specimens have not yet been described, and we emphasize that the morphology of the several available incisors from Maboko, Majiwa, and Kipsaramon is remarkably uniform and discretely different from that of K. wickeri at Fort Ternan.
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29
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0344394013
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note
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KNM-FT 28 has an index of relative canine height (crown height divided by maximum mesiodistal length) of 1.62. The value for the canine belonging to KNM-TH 28860 is 1.35. Ranges of values and sample sizes for Proconsul and Afropithecus are, respectively, 1.40 to 1.50 (9) and 1.14 to 1.18 (2); for Dryopithecus and Lufengpithecus values are 1.54 to 1.61 (3) and 1.56 to 1.85 (7).
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30
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0010962443
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G. Ll. Isaac and E. R. McCown, Eds. W. A. Benjamin, Menlo Park, CA
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31
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0003143294
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W. H. Kimbel and L. Martin, Eds. Plenum, New York
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L. Martin and P. Andrews, in Species, Species Concepts, and Primate Evolution, W. H. Kimbel and L. Martin, Eds. (Plenum, New York, 1993), pp. 393-427.
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32
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0001958723
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R. L. Bernor, V. Fahlbusch, H.-W. Mittman, Eds. Columbia Univ. Press, New York
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P. Andrews, T. Harrison, E. Delson, R. L. Bernor, L. Martin, in The Evolution of Western Eurasian Neogene Mammal Faunas, R. L. Bernor, V. Fahlbusch, H.-W. Mittman, Eds. (Columbia Univ. Press, New York, 1996), pp. 168-206.
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Martin, L.5
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33
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0344394011
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unpublished data
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4, and the maxilla.
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Kelley, J.1
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34
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0344825586
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note
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Two distinct lower canine morphologies are now recognized in the Paşalar sample. Canines belonging to the unnamed species are uniformly higher crowned in relation to length than those assigned to G. alpani.
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36
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0344394010
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note
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Andrews (12) proposed phyletic links between Kenyapithecus and all Turkish Middle Miocene taxa. We would restrict this relationship to the second, unnamed species at Paşalar.
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38
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0345256858
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note
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This research forms part of the work of the Baringo Paleontological Research Project (BPRP), in collaboration with the National Museums of Kenya. We thank the Office of the President of the Republic of Kenya for permission to carry out research in Kenya. BPRP has been supported by grants to A.H. from NSF (SBR-9208903), the Louise H. and David S. Ingalls Foundation, the Louise I. Brown Foundation, Clayton Stephenson, and Yale University. J.K. acknowledges support from NSF grant SBR-9408664 and thanks B. Alpagut who kindly gave permission to study the Paşalar hominoids. We thank E. Mbua and the staff of the National Museums of Kenya for their support; P. Andrews, T. Harrison, and D. Pilbeam for valuable insights regarding the relationships of Kenyapithecus; B. Kimeu, who discovered KNM-TH 28860; K. Cheboi for assistance in the field; and S. McBrearty, who suggested the generic name. L. Anderson, J. Kingston, and M. Tomasco prepared the figures.
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