author_facet Ruf, Irina
Luo, Zhe‐Xi
Wible, John R.
Martin, Thomas
Ruf, Irina
Luo, Zhe‐Xi
Wible, John R.
Martin, Thomas
author Ruf, Irina
Luo, Zhe‐Xi
Wible, John R.
Martin, Thomas
spellingShingle Ruf, Irina
Luo, Zhe‐Xi
Wible, John R.
Martin, Thomas
Journal of Anatomy
Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
Cell Biology
Developmental Biology
Molecular Biology
Ecology, Evolution, Behavior and Systematics
Histology
Anatomy
author_sort ruf, irina
spelling Ruf, Irina Luo, Zhe‐Xi Wible, John R. Martin, Thomas 0021-8782 1469-7580 Wiley Cell Biology Developmental Biology Molecular Biology Ecology, Evolution, Behavior and Systematics Histology Anatomy http://dx.doi.org/10.1111/j.1469-7580.2009.01059.x <jats:title>Abstract</jats:title><jats:p>The petrosal anatomy and inner ear structure of Jurassic cladotherian mammals represent the ancestral morphological conditions (groundplan) from which modern therian mammals (marsupials and placentals) have evolved. We present the reconstruction of the petrosal and inner ear features of the Late Jurassic dryolestoid mammal <jats:italic>Henkelotherium guimarotae</jats:italic> from high‐resolution computed tomography and three‐dimensional imaging analysis. This study of <jats:italic>Henkelotherium</jats:italic> revealed a combination of derived and primitive features, including: cladotherian apomorphies, such as the promontorial sulcus for the internal carotid artery and reduced lateral trough; trechnotherian characters, such as an enclosed cochlear canaliculus for the perilymphatic duct, post‐promontorial tympanic sinus and caudal tympanic process; in addition to plesiomorphic mammalian features, such as the cavum supracochleare and prootic canal. The inner ear of <jats:italic>Henkelotherium</jats:italic> shows a division between the utricle and saccule, a cochlear canal coiled through at least 270°, a distinctive primary bony lamina for the basilar membrane, and a secondary bony lamina. The development of the primary and secondary bony laminae in the cochlear canal is suggested here to be correlated with the concurrent coiling of the bony canal and membranous duct of the inner ear cochlea, apomorphies of the more inclusive cladotherian clade that also represent the ancestral morphotype of modern therian mammals. Because these features are crucial for high‐frequency hearing in extant therian mammals, their early appearance in Late Jurassic cladotherians suggests a more ancient origination for high‐frequency hearing in mammalian history than previously thought.</jats:p> Petrosal anatomy and inner ear structures of the Late Jurassic <i>Henkelotherium </i>(Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals Journal of Anatomy
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title Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_unstemmed Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_full Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_fullStr Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_full_unstemmed Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_short Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_sort petrosal anatomy and inner ear structures of the late jurassic <i>henkelotherium </i>(mammalia, cladotheria, dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
topic Cell Biology
Developmental Biology
Molecular Biology
Ecology, Evolution, Behavior and Systematics
Histology
Anatomy
url http://dx.doi.org/10.1111/j.1469-7580.2009.01059.x
publishDate 2009
physical 679-693
description <jats:title>Abstract</jats:title><jats:p>The petrosal anatomy and inner ear structure of Jurassic cladotherian mammals represent the ancestral morphological conditions (groundplan) from which modern therian mammals (marsupials and placentals) have evolved. We present the reconstruction of the petrosal and inner ear features of the Late Jurassic dryolestoid mammal <jats:italic>Henkelotherium guimarotae</jats:italic> from high‐resolution computed tomography and three‐dimensional imaging analysis. This study of <jats:italic>Henkelotherium</jats:italic> revealed a combination of derived and primitive features, including: cladotherian apomorphies, such as the promontorial sulcus for the internal carotid artery and reduced lateral trough; trechnotherian characters, such as an enclosed cochlear canaliculus for the perilymphatic duct, post‐promontorial tympanic sinus and caudal tympanic process; in addition to plesiomorphic mammalian features, such as the cavum supracochleare and prootic canal. The inner ear of <jats:italic>Henkelotherium</jats:italic> shows a division between the utricle and saccule, a cochlear canal coiled through at least 270°, a distinctive primary bony lamina for the basilar membrane, and a secondary bony lamina. The development of the primary and secondary bony laminae in the cochlear canal is suggested here to be correlated with the concurrent coiling of the bony canal and membranous duct of the inner ear cochlea, apomorphies of the more inclusive cladotherian clade that also represent the ancestral morphotype of modern therian mammals. Because these features are crucial for high‐frequency hearing in extant therian mammals, their early appearance in Late Jurassic cladotherians suggests a more ancient origination for high‐frequency hearing in mammalian history than previously thought.</jats:p>
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author Ruf, Irina, Luo, Zhe‐Xi, Wible, John R., Martin, Thomas
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description <jats:title>Abstract</jats:title><jats:p>The petrosal anatomy and inner ear structure of Jurassic cladotherian mammals represent the ancestral morphological conditions (groundplan) from which modern therian mammals (marsupials and placentals) have evolved. We present the reconstruction of the petrosal and inner ear features of the Late Jurassic dryolestoid mammal <jats:italic>Henkelotherium guimarotae</jats:italic> from high‐resolution computed tomography and three‐dimensional imaging analysis. This study of <jats:italic>Henkelotherium</jats:italic> revealed a combination of derived and primitive features, including: cladotherian apomorphies, such as the promontorial sulcus for the internal carotid artery and reduced lateral trough; trechnotherian characters, such as an enclosed cochlear canaliculus for the perilymphatic duct, post‐promontorial tympanic sinus and caudal tympanic process; in addition to plesiomorphic mammalian features, such as the cavum supracochleare and prootic canal. The inner ear of <jats:italic>Henkelotherium</jats:italic> shows a division between the utricle and saccule, a cochlear canal coiled through at least 270°, a distinctive primary bony lamina for the basilar membrane, and a secondary bony lamina. The development of the primary and secondary bony laminae in the cochlear canal is suggested here to be correlated with the concurrent coiling of the bony canal and membranous duct of the inner ear cochlea, apomorphies of the more inclusive cladotherian clade that also represent the ancestral morphotype of modern therian mammals. Because these features are crucial for high‐frequency hearing in extant therian mammals, their early appearance in Late Jurassic cladotherians suggests a more ancient origination for high‐frequency hearing in mammalian history than previously thought.</jats:p>
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spelling Ruf, Irina Luo, Zhe‐Xi Wible, John R. Martin, Thomas 0021-8782 1469-7580 Wiley Cell Biology Developmental Biology Molecular Biology Ecology, Evolution, Behavior and Systematics Histology Anatomy http://dx.doi.org/10.1111/j.1469-7580.2009.01059.x <jats:title>Abstract</jats:title><jats:p>The petrosal anatomy and inner ear structure of Jurassic cladotherian mammals represent the ancestral morphological conditions (groundplan) from which modern therian mammals (marsupials and placentals) have evolved. We present the reconstruction of the petrosal and inner ear features of the Late Jurassic dryolestoid mammal <jats:italic>Henkelotherium guimarotae</jats:italic> from high‐resolution computed tomography and three‐dimensional imaging analysis. This study of <jats:italic>Henkelotherium</jats:italic> revealed a combination of derived and primitive features, including: cladotherian apomorphies, such as the promontorial sulcus for the internal carotid artery and reduced lateral trough; trechnotherian characters, such as an enclosed cochlear canaliculus for the perilymphatic duct, post‐promontorial tympanic sinus and caudal tympanic process; in addition to plesiomorphic mammalian features, such as the cavum supracochleare and prootic canal. The inner ear of <jats:italic>Henkelotherium</jats:italic> shows a division between the utricle and saccule, a cochlear canal coiled through at least 270°, a distinctive primary bony lamina for the basilar membrane, and a secondary bony lamina. The development of the primary and secondary bony laminae in the cochlear canal is suggested here to be correlated with the concurrent coiling of the bony canal and membranous duct of the inner ear cochlea, apomorphies of the more inclusive cladotherian clade that also represent the ancestral morphotype of modern therian mammals. Because these features are crucial for high‐frequency hearing in extant therian mammals, their early appearance in Late Jurassic cladotherians suggests a more ancient origination for high‐frequency hearing in mammalian history than previously thought.</jats:p> Petrosal anatomy and inner ear structures of the Late Jurassic <i>Henkelotherium </i>(Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals Journal of Anatomy
spellingShingle Ruf, Irina, Luo, Zhe‐Xi, Wible, John R., Martin, Thomas, Journal of Anatomy, Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals, Cell Biology, Developmental Biology, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Histology, Anatomy
title Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_full Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_fullStr Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_full_unstemmed Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_short Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_sort petrosal anatomy and inner ear structures of the late jurassic <i>henkelotherium </i>(mammalia, cladotheria, dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
title_unstemmed Petrosal anatomy and inner ear structures of the Late Jurassic Henkelotherium (Mammalia, Cladotheria, Dryolestoidea): insight into the early evolution of the ear region in cladotherian mammals
topic Cell Biology, Developmental Biology, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Histology, Anatomy
url http://dx.doi.org/10.1111/j.1469-7580.2009.01059.x