Wall thickness of gas- and marrow-filled avian long bones: Measurements on humeri, femora and tibiotarsi in crows ( Corvus corone cornix) and magpies ( Pica pica)

We studied how the ratio K of the internal to external diameter of gas- and marrow-filled avian long bones follows the biomechanical optima derived for tubular bones with minimum mass designed to fulfil various mechanical requirements. We evaluated radiographs of numerous humeri, femora and tibiotar...

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Veröffentlicht in:Journal of biomechanics 2006-01, Vol.39 (11), p.2140-2144
Hauptverfasser: Suhai, Bence, Gasparik, Mihály, Csorba, Gábor, Gerics, Balázs, Horváth, Gábor
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container_end_page 2144
container_issue 11
container_start_page 2140
container_title Journal of biomechanics
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creator Suhai, Bence
Gasparik, Mihály
Csorba, Gábor
Gerics, Balázs
Horváth, Gábor
description We studied how the ratio K of the internal to external diameter of gas- and marrow-filled avian long bones follows the biomechanical optima derived for tubular bones with minimum mass designed to fulfil various mechanical requirements. We evaluated radiographs of numerous humeri, femora and tibiotarsi in Corvus corone cornix and Pica pica. The K-values of the gas-filled humerus ( K = 0.78 ± 0.03 ) and the marrow-filled femur ( K = 0.79 ± 0.02 ) in Corvus are practically the same, while K of the marrow-filled tibiotarsus ( K = 0.71 ± 0.04 ) is significantly smaller. The same is true for the gas-filled humerus ( K = 0.78 ± 0.02 ) and the marrow-filled femur ( K = 0.77 ± 0.02 ) and tibiotarsus ( K = 0.67 ± 0.05 ) in Pica. K in Corvus is slightly larger than K in Pica, but the differences are statistically not significant. The standard deviation Δ K of the tibiotarsi ( Δ K = 0.04 – 0.05 ) is approximately two times as large as that of the humeri ( Δ K = 0.02 – 0.03 ) and femora ( Δ K = 0.02 ) in both species. Accepting the assumption of earlier authors that the ratio Q of the marrow to bone density is 0.5, our data show that the marrow-filled tibiotarsi of Corvus and Pica are optimized for stiffness, while the marrow-filled femora are far from any optimum. The relative wall thickness W = 1 - K of the gas-filled avian humeri studied is much larger than the theoretical optimum W * = 1 - K * = 0.07 , and thus these bones are thicker-walled than the optimal gas-filled tubular bone with minimum mass.
doi_str_mv 10.1016/j.jbiomech.2005.06.013
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We evaluated radiographs of numerous humeri, femora and tibiotarsi in Corvus corone cornix and Pica pica. The K-values of the gas-filled humerus ( K = 0.78 ± 0.03 ) and the marrow-filled femur ( K = 0.79 ± 0.02 ) in Corvus are practically the same, while K of the marrow-filled tibiotarsus ( K = 0.71 ± 0.04 ) is significantly smaller. The same is true for the gas-filled humerus ( K = 0.78 ± 0.02 ) and the marrow-filled femur ( K = 0.77 ± 0.02 ) and tibiotarsus ( K = 0.67 ± 0.05 ) in Pica. K in Corvus is slightly larger than K in Pica, but the differences are statistically not significant. The standard deviation Δ K of the tibiotarsi ( Δ K = 0.04 – 0.05 ) is approximately two times as large as that of the humeri ( Δ K = 0.02 – 0.03 ) and femora ( Δ K = 0.02 ) in both species. Accepting the assumption of earlier authors that the ratio Q of the marrow to bone density is 0.5, our data show that the marrow-filled tibiotarsi of Corvus and Pica are optimized for stiffness, while the marrow-filled femora are far from any optimum. 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We evaluated radiographs of numerous humeri, femora and tibiotarsi in Corvus corone cornix and Pica pica. The K-values of the gas-filled humerus ( K = 0.78 ± 0.03 ) and the marrow-filled femur ( K = 0.79 ± 0.02 ) in Corvus are practically the same, while K of the marrow-filled tibiotarsus ( K = 0.71 ± 0.04 ) is significantly smaller. The same is true for the gas-filled humerus ( K = 0.78 ± 0.02 ) and the marrow-filled femur ( K = 0.77 ± 0.02 ) and tibiotarsus ( K = 0.67 ± 0.05 ) in Pica. K in Corvus is slightly larger than K in Pica, but the differences are statistically not significant. The standard deviation Δ K of the tibiotarsi ( Δ K = 0.04 – 0.05 ) is approximately two times as large as that of the humeri ( Δ K = 0.02 – 0.03 ) and femora ( Δ K = 0.02 ) in both species. Accepting the assumption of earlier authors that the ratio Q of the marrow to bone density is 0.5, our data show that the marrow-filled tibiotarsi of Corvus and Pica are optimized for stiffness, while the marrow-filled femora are far from any optimum. The relative wall thickness W = 1 - K of the gas-filled avian humeri studied is much larger than the theoretical optimum W * = 1 - K * = 0.07 , and thus these bones are thicker-walled than the optimal gas-filled tubular bone with minimum mass.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>16084519</pmid><doi>10.1016/j.jbiomech.2005.06.013</doi><tpages>5</tpages></addata></record>
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subjects Animal behavior
Animals
Biomechanical Phenomena
Biomechanics
Black-billed magpie ( Pica pica)
Bone density
Bone Marrow - anatomy & histology
Bone mechanics
Crows - anatomy & histology
Femur
Femur - anatomy & histology
Gas- and marrow-filled tubular bones
Gases
Hooded crow ( Corvus corone cornix)
Humerus
Humerus - anatomy & histology
Hypotheses
Optimum structure
Songbirds - anatomy & histology
Standard deviation
Studies
Tibia - anatomy & histology
Tibiotarsus
Wall thickness
title Wall thickness of gas- and marrow-filled avian long bones: Measurements on humeri, femora and tibiotarsi in crows ( Corvus corone cornix) and magpies ( Pica pica)
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