LONG BONE HISTOLOGY OF THE HADROSAURID DINOSAUR MAIASAURA PEEBLESORUM: GROWTH DYNAMICS AND PHYSIOLOGY BASED ON AN ONTOGENETIC SERIES OF SKELETAL ELEMENTS

By J. Horner, A. de Ricqlès, Kevin Padian. 2000

363 citations recorded by the source corpus.

Subfields: Computer Vision and Pattern Recognition, Nature and Landscape Conservation, Paleontology

View Paper: https://www.semanticscholar.org/paper/fa725a2343e794a0f46aa5731439e21ac10f0c7a

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Computer Vision and Pattern Recognition

1. J. Horner
2. A. de Ricqlès
3. Kevin Padian
4. H. Woodward
5. J. Castanet

In Nature and Landscape Conservation

1. J. Horner
2. Kevin Padian
3. A. de Ricqlès
4. S. Nesbitt
5. J. Castanet
6. J. Cubo
7. N. Le Roy
8. Cayetana Martínez-Maza

In Paleontology

1. J. Horner
2. S. Nesbitt
3. Kevin Padian
4. Michel Laurin
5. A. de Ricqlès
6. J. Castanet
7. H. Woodward
8. C. Griffin

Citations in the corpus

• OSTEOHISTOLOGY OF CONFUCIUSORNIS SANCTUS (THEROPODA: AVES) (2003, methodology): “These are commonly encountered even in the bones of juvenile hadrosaurs and other large dinosaurs (Horner et al., 1999, 2000), but seldom in much smaller animals such as flying birds until the adult stage is reached.”
• First histological and skeletochronological data on temnospondyl growth: palaeoecological and palaeoclimatological implications (2004, background): “Bone histology and skeletochronology are increasingly used to gain insights into the biology of extinct amniotes such as Mesozoic reptiles (e.g. Horner et al., 2000) or Cenozoic mammals (e.g. Buffrénil et al., 1990).”
• Modeling growth rates for sauropod dinosaurs (2008, background): “However, some studies have demonstrated that the number of growth lines may vary even between different skeletal elements in the same individual (e.g., Horner et al. 2000) and so their varied development would result in different model growth curves.”
• Dinosaurs and the island rule: The dwarfed dinosaurs from Haţeg Island (2010, background): “10c) showdense secondary remodelling in the inner cortex, but secondary osteons becomemore scattered closer to the surface of the bone, similar to remodelling of adult specimens of the hadrosaurMaiasaura peeblesorum (Horner et al., 2000).”
• BONE HISTOLOGY AND GROWTH PATTERNS OF SOME NONMAMMALIAN THERAPSIDS (2004, background): “Previous work on osteohistology has contributed significantly to understanding various aspects of the biology of dinosaurs and other archosaurs (e.g., Reid, 1984, Ricqlès, 1983; Chinsamy, 1993a, b; Varricchio, 1993; Curry, 1999; Horner et al. 2000, 2001; Chinsamy and Elzanowski, 2001).”
• Paleohistological estimation of bone growth rate in extinct archosaurs (2012, background): “…growth trajectories in body mass (Erickson 2005; Bybee et al. 2006), age at sexual maturity (Lee and Werning 2008), bone growth rates (Curry 1999; Horner et al. 1999, 2000, 2001; Sander 2000; Padian et al. 2001, 2004; Ricqlès et al. 2003, 2008; Cooper et al. 2008), and metabolic rates (Ricqlès…”
• The evolution and function of thyreophoran dinosaur scutes: implications for plate function in stegosaurs (2005, methodology): “Thin-sections were processed and observed according to standard techniques (e.g., Wilson 1994; Horner et al. 2000).”