Literature DB >> 848569

The evolution of molar occlusion in the Cercopithecidae and early Catarrhines.

R F Kay.   

Abstract

Those Eocene prosimians which are possible catarrhine ancestors have four blade-like crests on each lower molar. Each crest shears in sequence across two upper molar crests. Occluding crests are concavely curved to hold the foods being sheared. Each of two medial lower molar crests bordering the principal crushing surface shear past single upper molar crests at about the same time the lateral lower molar crests contact the second rank of upper molar crests. Grinding and crushing areas are restricted to hypoconid, trigonid, and protocone surfaces. Oligocene catarrhine molars have increased crushing-grinding capacities and maintained but modify their shearing. As the crushing surface of the protocone expands and a crushing hypocone is added, the "second rank" upper molar shearing crests are functionally reduced. At the same time medial crests are increasingly emphasized so that the total shearing capacity remains virtually unchanged. Marginal shearing blades are straight edged; leading edges of occluding blades are set at different angles to the occlusal plane so that blades contact at only one point at any given time. Early Primates have separate crushing basins surrounded by shearing blades. Catarrhines tend to link explanding crushing surfaces anteroposteriorly into a continuous surface between all molars. A cladistic analysis based on both new and previously recognized characters indicates that: 1. Apidium may be more closely related to Aegyptopithecus than to Parapithecus; 2. cercopithecids are derived from a Parapithecus-related stock; 3. Oreopithecus could equally well have come from an Apidium or Aegyptopithecus stock.

Mesh:

Year:  1977        PMID: 848569     DOI: 10.1002/ajpa.1330460213

Source DB:  PubMed          Journal:  Am J Phys Anthropol        ISSN: 0002-9483            Impact factor:   2.868


  17 in total

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3.  Reproductive fitness and tooth wear: milking as much as possible out of dental topographic analysis.

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4.  How could sympatric megaherbivores coexist? Example of niche partitioning within a proboscidean community from the Miocene of Europe.

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5.  Using occlusal wear information and finite element analysis to investigate stress distributions in human molars.

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6.  Primitive Old World monkey from the earliest Miocene of Kenya and the evolution of cercopithecoid bilophodonty.

Authors:  D Tab Rasmussen; Anthony R Friscia; Mercedes Gutierrez; John Kappelman; Ellen R Miller; Samuel Muteti; Dawn Reynoso; James B Rossie; Terry L Spell; Neil J Tabor; Elizabeth Gierlowski-Kordesch; Bonnie F Jacobs; Benson Kyongo; Mathew Macharwas; Francis Muchemi
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7.  Additional materials of Myanmarpithecus yarshensis (Amphipithecidae, Primates) from the middle Eocene Pondaung Formation.

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Review 8.  Why are there apes? Evidence for the co-evolution of ape and monkey ecomorphology.

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9.  Genetic integration of molar cusp size variation in baboons.

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Journal:  Am J Phys Anthropol       Date:  2010-06       Impact factor: 2.868

10.  Molar macrowear reveals Neanderthal eco-geographic dietary variation.

Authors:  Luca Fiorenza; Stefano Benazzi; Jeremy Tausch; Ottmar Kullmer; Timothy G Bromage; Friedemann Schrenk
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