Medullary bone is an ephemeral type of bone tissue, today found only in sexually mature female birds, that provides a calcium reservoir for eggshell formation. The presence of medullary bone-like tissues in extant birds, pterosaurs, and dinosaurs distantly related to birds shows that caution must be exercised before concluding that fossils bear medullary bone. Here we describe a new specimen of pengornithid enantiornithine from the Lower Cretaceous Jiufotang Formation. Consisting of an isolated left hindlimb, the three-dimensional preservation contrasts with the crushed preservation characteristic of most Jehol specimens. Histological examinations suggest this resulted from the presence of a thick layer of highly vascular bone spanning the medullary cavities of the femur and tibiotarsus, consistent with expectations for medullary bone in extant birds. Micro-computed tomographic scans reveal small amounts of the same tissue extending into the pedal phalanges. We consider the tissue to be homologous to the medullary bone of Neornithines.
Medullary bone (MB) is an ephemeral bone tissue known only in extant female birds (Neornithes) that provides a rapidly mobilized calcium reservoir for eggshell production and is metabolized in response to elevated levels of estrogen1,2,3,4,5. The name is a misnomer, for although the tissue is most conspicuous in the medullary cavities of avian long bones, it also forms in cancellous spaces throughout the appendicular and axial skeleton2. Non-avian MB was first suggested to be present in non-avian dinosaurs (hereafter dinosaurs) based on unusual osseous tissues found in the femur of Tyrannosaurus rex MOR (Museum of the Rockies, Bozeman, MT, USA) 11256. In addition to further supporting the ancestral link between birds and theropod dinosaurs7,8, this discovery implied this “avian” feature arose surprisingly deep in the dinosaurian tree. Since this discovery, MB (or tissues resembling it, see below) has been described in other dinosaurs, some of which are more distantly related to birds including: two ornithopods—Dysalotosaurus and Tenontosaurus9,10; two non-avian theropods—Allosaurus9 and an additional Tyrannosaurus specimen11; and two sauropodomorphs—Mussaurus12 and a saltasaurine titanosaur13. Tissues resembling MB have also been observed in two non-dinosaurian ornithodirans, Pterodaustro14 and Bakonydraco15.
Definitive identification of MB in fossil taxa is problematic. Osseous tissues that can be misconstrued for MB (medullary bone-like tissues; MBL) are commonplace in the bones of tetrapods, particularly in the hollow long bones of ornithodirans. Tissues with the potential to appear like MB include: endosteal bone lining medullar cavities16; mechanically supporting trabeculae17; and trabecular remnants of former metaphyses moved into the diaphyses during ontogeny16. In addition, Chinsamy and Tumarkin-Deratzian18 showed that tissues remarkably similar to MB occur in some pathological avian bones. Finally, Prondvai and Stein15, Chinsamy and colleagues13, and Prondvai19 have reported MBL with unknown functionality in non-pathological and presumably non-reproductive (rapidly growing, juvenile) dinosaurs and pterosaurs. These issues show that caution should be exercised before concluding that MB reflecting sex and reproductive status is truly present in fossils15,18,19,20. Because of such concerns Schweitzer and colleagues21 tried to provide additional support for the presence of MB in Tyrannosaurus rex MOR 1125 by means of histochemical analyses. They found that MB in extant ovipositing birds shows significantly greater amounts of glycosaminoglycans, and specifically keratan sulfate, than in the cortical bone (CB). MOR 1125 showed a similar pattern. Nevertheless, subsequent preliminary work by Canoville and colleagues22 suggests that pathological bone forming in medullary cavities can also show elevated levels of keratan sulphate. Further testing is required before chemical signatures can serve as a viable means to test for MB in fossils.
The identification of MB in non-avian fossil archosaurs as a means to determine sex and reproductive activity was based on three histological characteristics: (1) location in the medullary cavity; (2) an endosteal origin, marked by a resorption line between the cortex and the hypothetical MB; and (3) a woven arrangement of the collagen fibers, suggesting rapid bone deposition. Given the factors noted above that can produce MBL, these criteria in and of themselves cannot differentiate MB from MBL18,19. Hence, some past identifications of MB may be incorrect12,20. More precisely, MB is always endosteal in origin (Table 1; Criterion 2), but as previously mentioned, it also forms in cancellous spaces of bones without medullary cavities sensu stricto (e.g., in flat bones of the skull, irregular bones like vertebrae) (Criterion 1). Furthermore, recent studies indicate that MB may form more slowly in some large ratites (possibly due to their large size), which has been interpreted as both lamellar6,22 and parallel fibered (Criterion 3)19.
MB varies in neornithines, ranging in thickness, skeletal distribution, and orientation of collagen fibers6,21. We propose that through a greater number of criteria (Table 1) researchers can better identify probable MB in fossils. In addition to the three previously mentioned criteria, MB should have the following additional six characteristics (Table 1): (4) the periosteal surfaces should be free from indication of pathology [unlike in Allosaurus UUVP (Utah Museum of Natural History, Salt Lake City, UT, US.) 5300 in which the periosteum bears a callus]18; (5) the MB should line the majority of the medullary cavity [unlike the condition in Dysalotosaurus SMNS (Staatliches Museum für Naturkunde, Stuttgart, Germany) T3];10 (6) the MB should be clearly demarcated from the CB without a graded transition allowing the MB to often show separation from the cortex during diagenesis;2,6 (7) the MB should occur in multiple skeletal elements [in neornithines MB is most commonly seen in the long bones of the hindlimb23, most prevalently expressed in the femur1, and is universally present in the tibiotarsus22. However, in neornithines MB can form extensively throughout the entire skeleton, reportedly occurring in the skull bones and pedal phalanges of some taxa2,24; (8) MB should coincide with a reduced growth rate associated with the onset of reproduction making it unlikely to occur in young, rapidly growing individuals [MB in juvenile Tyrannosaurus BMRP (Burpee Museum of Natural History, Rockford, Illinois, USA) 2006.4.4 is likely pathological11; and finally (9) MB may have vascular sinuses arranged in doublet, triplet or greater patterns (this last criterion may further characterize MB but does not appear to be universally present6).
Here we describe a new specimen of pengornithid enantiornithine bird from the Early Cretaceous Jiufotang Formation of China, which records the youngest stage of the Lower Cretaceous Jehol Biota (Fig. 1). Using gross morphology, histologic microstructure, tissue distributions, comparison with neornithines and purported non-neornithine fossil MB, and the nine aforementioned neornithine MB correlates, we demonstrate that the new specimen bears what is best interpreted as MB in its long bones. This represents the most compelling evidence for MB in a Mesozoic bird at this time, strongly suggesting this tissue evolved outside the crown lineage.
The new specimen IVPP (Institute of Vertebrate Paleontology and Paleoanthroplogy, Chinese Academy of Sciences, Beijing, China) V15576 is an isolated, articulated left hindlimb preserved in three dimensions. This stands in contrast to the typically crushed preservation of most other Jehol specimens (Fig. 1). Traces of crural feathers are weakly preserved. The fossil was collected by an IVPP team in the Lower Cretaceous Jiufotang Formation25 near Chifeng, Inner Mongolia Autonomous Region, China. The presence of a femur nearly as long as the tibiotarsus, elongate fibula subequal in length to the tibia, presence of metatarsal V, and a proportionately elongate metatarsal I (38% length of metatarsal III; 33–42% in pengornithids) and hallux clearly allow referral of IVPP V15576 to the Pengornithidae, a diverse clade of basal enantiornithines26. This is the first pengornithid collected from Inner Mongolia, but without additional material for the specimen, it cannot be identified to the generic level. IVPP V15576 (femur length, 38.8 mm; incomplete tibiotarsus, 37 mm; metatarsal III, 21.9 mm; metatarsal I, 8.4 mm) is similar in size to Parapengornis IVPP V18687 and pengornithid IVPP V16832 but much smaller than Pengornis houi IVPP V15536 (femur length, 48 mm)27,28. Unfortunately, the distal end of the tibiotarsus is not preserved and the proximal end of the tarsometatarsus is abraded, making it difficult to assess the degree of fusion among these compound elements. It appears fusion of the proximal tarsometatarsus may have been incomplete.
The transverse diaphyseal thin-section from the femur of IVPP V15576 reveals an external layer of CB ~190–290 µm in width, and a thicker more-vascularized layer (hereafter referred to as MB) between 440 and 890 µm in width that spans circumferentially around most of the medullar cavity (Fig. 2). The CB consists of poorly vascularized parallel-fibered bone with mostly simple, longitudinal vascular canals together with a few reticular canals. CB osteocyte lacunae are more organized and smaller than those found in the MB (Fig. 2d). The cortex is interrupted by a line of arrested growth (LAG) (Fig. 2c). No outer circumferential layer (OCL), nor inner circumferential layer (ICL) is present, suggesting that the bird had not reached skeletal maturity29,30. Near the caudal intermuscular line (a bony ridge extending distally from the caudal surface to the lateral surface that marks the boundary between the m. femorotibialis externus and femoral adductors)31,32 the LAG reaches the contact between the CB and MB (i.e., the LAG is obliterated by the resorption line). Opposite the intermuscular line the LAG approaches the periosteal surface. This presumably reflects extensive ontogenetic osseous drift33. The periosteal surface of the bone is smooth and lacks any indication of pathology18.
The contact between the CB and MB is uneven, with the characteristic scalloped resorption line created by osteoclasts34 prior to the deposition of MB in extant birds. The MB consists of extremely vascularized woven to parallel-fibered bone, with numerous radial vascular canals, and spicular trabeculae radiating inward towards the center of the medullary cavity. These are oriented approximately perpendicular to the periosteal surface. The vascular canals get wider as they approach the center of the medullary cavity. Opposite to the intermuscular line, a small area of MB located near the CB possesses a few canals organized into small groups within osteon-like structures (Fig. 2e). Some of those groups show a reticular pattern, while others are simply groups of longitudinal canals (Fig. 2e). The latter look extremely similar to the doublet and triplet vascular patterns, referred to as “vascular sinuses” in the MB of Tyrannosaurus rex and extant ratites (Fig. 3g and S3 in Schweitzer et al. 6). However, one of these triplet vascular sinuses appears to occur in the CB. Nearing these “vascular sinuses”, within the medullary cavity, a thick strut of avascular parallel-fibered bone is also lined with MB. Like the CB, the bone is birefringent and the osteocyte lacunae have a more organized appearance suggesting this may represent a trabecular strut. MB also develops on the naturally-occurring metaphyseal bone trabeculae of living birds21. Although not directly connected to the CB in our cross section, it may be that the trabecula extends into the medullary cavity at an angle passing through our sectioned plane (Fig. 2).
The contact between CB and MB is clearly visible under polarized light, with the MB being only weakly birefringent (Fig. 2b). This is consistent with relatively rapid deposition and a lower amount of collagen fibrils35. Rapid bone deposition is also suggested by the larger size and bulbous appearance of the osteocytes relative to those in the CB. The low birefringence suggests the MB may have formed more slowly than in most extant taxa. In one area the MB is preserved but not the CB, indicating weakness at the basal layer as in extant avian MB6. Notably, the MB is more than double the thickness of the CB in most of the femur. This is consistent with the peak condition in many modern birds during the last twelve hours before oviposition36.
The tibiotarsus suffered more diagenetic alteration than the femur. It is heavily crushed and the damage slightly obscures detailed observations that were feasible in the femur (Fig. 3a). Its cortex is thinner than that of the femur (180–190 µm), with a larger medullary cavity and a proportionately thinner layer of MB (360–580 µm). This condition is also observed in living birds1. The CB consists of parallel-fibered bone, with simple, longitudinal canals located close to the periosteal surface. No LAG, OCL, nor ICL can be confidently identified. As in the femur, the MB consists of both woven and parallel-fibered bone. Osteocyte lacunae also are generally smaller in the tibiotarsus when compared to those in the femur. In some places the MB and CB are delaminated (Fig. 3).
Computed tomographic (CT) scans of pedal phalanges
A crack allowed for a portion of the slab containing the distal pedal phalanges to be removed (Fig. 1) and µCT scanned (Fig. 4). Although these scans do not provide a detailed histological examination (e.g., no osteocyte lacunae, no collagen fiber orientation), they do show some useful microarchitectural details. Notably, they reveal small amounts of MB in the non-ungual pedal phalanges. This tissue is easily identified by its cancellous architecture within the medullary cavity in longitudinal view (Fig. 4a). In cross-section a faint line can be seen demarcating the internal MB and the external CB (Fig. 4b).
Comparison with neornithines
IVPP V15576 preserves unusual bone tissue in the medullary cavities (Criterion 1) of the hindlimb bones. As in the MB of living birds, the tissue is clearly endosteal in origin as indicated by the presence of a resorption tideline (Criterion 2). The MB in IVPP V15576 is weakly birefringent compared to the CB (Fig. 2b), consistent with relatively rapid deposition (Criterion 3)35. The tissue is primarily woven but also somewhat parallel-fibered in both the femur and tibiotarsus (Criterion 3). This is consistent with observations of some paleognath neornithines21. The periosteal surfaces of all the preserved elements in IVPP V15576 are smooth, without indication of pathology (Criterion 4). As in most living birds, the cancellous bone tissue in IVPP V15576 is found lining nearly the entire medullary cavity (Criterion 5) and has a clearly visible limit with the CB, often leading to delamination in fossils (Criterion 6). In one area the MB is preserved but not the CB, indicating weakness at the basal layer as in extant avian MB (Criterion 6)6. The MB is found throughout the preserved elements indicative of a systemic process. Where preservation permits comparison (only hindlimb), IVPP 15576 matches living birds in extent and distribution (Criterion 7), being most strongly developed in the femur (Fig. 2)1. The tissue apparently extends into the non-ungual pedal phalanges (Fig. 4), where it is known to occur in some extant neornithine taxa2. The CB of the femur is poorly vascularized and interrupted by a LAG indicating a period of reduced growth rate. This strongly suggests that IVPP V15576 was not a rapidly growing subadult (Criterion 8). Vascular sinuses arranged in triplet and doublet patterns like those reported in the MB of some extant birds and T. rex (MOR 1125)6 are also present in the femoral section of IVPP V15576 (Fig. 2e) (Criterion 8; Tables 1, 2). In IVPP V15576 MB is found on the trabecular strut, consistent with the naturally occurring metaphyseal bone trabeculae in living birds21. Comparison of the purported MB in IVPP V15576 with living, reproductively active female birds reveals no observable differences. Thus we conclude that this fossil bird preserves MB homologous to that in female neornithines.
IVPP V15576 preserves what we interpret as extensive MB throughout the femur and tibiotarsus (Figs. 2,3) that likely extended into the non-ungual pedal phalanges (Fig. 4). This represents the only demonstrated occurrence of MB in the Enantiornithes, the dominant clade of terrestrial birds during the Cretaceous. Furthermore, according to our proposed criteria for identifying MB in fossils, IVPP V15576 preserves the most credible evidence of this tissue’s presence in a non-neornithine archosaur thus far (Table 2; see Supplementary Note 1).
Among Mesozoic birds, MB has been previously reported only in the basal pygostylian, Confuciusornis (Aves: Pygostylia) DNHM (Dalian Natural History Museum, Dalian, China) D187437. Although the humerus, ulna, and tibiotarsus were all sampled, MB was only found in the humerus and to a lesser extent in the ulna. This contrasts with the distribution in extant ovipositing birds where all studied taxa show the presence of MB in the tibiotarsus22. Differences in bone texture (i.e., cancellous versus compact) are cited in support of the interpretation of small bone fragments in the medullary cavity of the humerus as representing MB37. However, the alleged MB is very limited in distribution and associated with fragments that are most likely from the cortex. Thus, based on our more stringent criteria, evidence for MB in this specimen is equivocal at best (Table 2). However, if this identification is correct, it is notable that the MB is most developed in the humerus and not at all present in the tibiotarsus. This is in stark contrast to MB in all studied extant neornithines22. The pattern in Confuciusornis is opposite to that observed in most living birds, in which the pneumatic humeri contain very little MB and the femora and tibiotarsi have the most2. If in fact the tissue is MB, the findings may be the result of the fact the humerus was probably apneumatic in basal birds38, suggesting some early birds distributed MB in the skeleton differently from extant neornithine taxa.
If conclusions about the presence of MB in the pengornithid IVPP V15576 are correct, this specimen represents a reproductively active female. The presence of vascular canals close to the periosteum and the absence of an OCL indicate IVPP V15576 was still actively growing at the time of death, confirming inferences that enantiornithines, like non-avian dinosaurs9,39 reached reproductive maturity (RM) before somatic maturity (SM). This is unlike the condition observed in most neornithines, in which RM is coincident with SM29,40 (although some neornithines have secondarily evolved protracted growth)41. Assuming this represents the primitive condition at the base of Aves, this suggests that the modern condition seen in living birds (i.e., RM after SM) is limited to a subset of the Ornithuromorpha. The LAG present in the femur of IVPP V15576 may represent the acquisition of RM, as suggested in a previously described enantiornithine preserving similar histological features9,29. The CB of IVPP V15576 shows vascularization after the inferred acquisition of RM, whereas the CB becomes avascular after the deposition of the double-LAG in the femur of enantiornithine STM (Shandong Tianyu Museum of Nature, Pingyi, China) 29-829. This adds to the mounting body of evidence that enantiornithines were diverse in their growth strategies42. This is true even within the Pengornithidae; although nearly the same size, the slightly larger Parapengornis IVPP V18687 (femur length, 39.8 mm) preserves very different femoral histology with much greater vascularization and no LAGs or ICL. These are features consistent with a younger, more rapidly growing individual27.
Two Early Cretaceous birds preserving ovarian follicles were not found to show MB29. There are three possible interpretations for this absence: the circular structures preserved in the abdominal cavity of Jeholornis STM2-51 and enantiornithine STM29-8 in fact do not represent ovarian follicles43; taphonomy resulted in the loss of this delicate feature; or MB was not yet present at the time of death in these specimens. The latter implies the follicles were not as mature as previously inferred29,44. Rapid yolk deposition is inferred to be absent in enantiornithines and thus folliculogenesis most likely occurred over an extended period, as in crocodylians45. This could explain the relatively large number of specimens found preserving follicles (n = 10)45,46. In pigeons, MB only appears a few days before ovulation1 and in some taxa MB is only present for a matter of hours23. Given the ephemeral nature of avian MB, its absence in the two sampled specimens preserving developing follicles is not surprising. However, in enantiornithines the presence of MB may have persisted for slightly longer intervals than in neornithines. Consistent with the slower growth rates observed in enantiornithines29,30,47 and perhaps an extended period of reproductive activity, the MB tissue in IVPP V15576 appears to be less woven than in most neornithines, also including some parallel-fibered tissue. This suggests enantiornithine MB, like enantiornithine CB, may have formed at a slower rate than that of most similarly sized modern birds.
Because pathological endosteal tissues resembling MB can form in extant birds and MBL occurs in fossils lacking identifiable evidence for both reproductive activity and pathology, unequivocal identification of MB requires more than morphological similarity (Tables 1, 2). Work has already begun to identify a unique histochemical signature able to identify MB in well preserved fossils (Criterion 10)21. However, further analysis is required before it will be possible to definitively identify MB through such methods22. Therefore, at this time, no published non-neornithine specimen preserving MB can be unequivocally identified as such. MB is also characterized by (Criterion 11) a lower content of collagen fibrils and a higher degree of calcification1 and it may be possible in the future to develop techniques allowing the determination of these characteristics in the MB of IVPP V15576 using SEM, microradiography, microCT, and/or other methodologies. In summation, pending potential future histochemical analyses and the development of new techniques, we suggest the cancellous MB tissue present in the medullary cavity of the femur, tibiotarsus, and non-ungual pedal phalanges in IVPP V15576 most likely represents MB based on standard paleohistological examinations.
The femoral diaphysis sample was extracted using a micro-saw and embedded in a clear epoxy resin (Epoxyset; Allied High Tech Products Inc., Rancho Dominguez, CA, USA). The sample was serially sectioned in the transverse plane in 1.5 mm increments using a slow-speed diamond saw (Isomet 1000; Buehler Inc., Lake Bluff IL, USA). The sections were affixed to petrographic microscope slides using epoxy and rotary-sanded (Rotopol 11; Struers Inc., Cleveland, OH, USA) to ~ 100 μm thickness using descending grades (220–1200 grit) of carbide sandpaper using water as a lubricant then polished using an alumina slurry. The femur was visualized and photographed using both incident light SZX12; Olympus Inc., Tokyo Japan) and polarized petrographic microscopy (BX60; Olympus Inc., Tokyo Japan).
The tibiotarsus sample was taken using a micro-saw, embedded in EXAKT Technovit 7200 one-component resin, and allowed to dry for 24 h. The sample was then cut and polished until the desired optical contrast was reached (slice thickness between 100 and 150 µm). The sample was viewed under normal and polarized light using a Leica DM- RX polarizing microscope. It was photographed using a Zeiss AxioCam MRc5 and using the Axiovision SE66 4.9 software. Measurements were taken with the computer software Fiji (ImageJ) v.1.0.
The specimen was scanned using the 225-kV micro-CT at the Key Laboratory of Vertebrate Evolution and Human Origin of CAS, IVPP, CAS, Beijing, China. The part of the slab containing the pedal phalanges was removed from the main block along an existing crack and scanned at a detector resolution of 7.8 μm per pixel, and three-dimensional reconstructions were created with the software Avizo (version 8.1).
IVPP V15576 is reposited at the Institute of Vertebrate Paleontology in Beijing. All data are available upon reasonable request.
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Bloom, W., Bloom, M. A. & McLean, F. C. Calcification and ossification. Medullary bone changes in the reproductive cycle of female pigeons. Anat. Rec. 81, 443–475 (1941).
Taylor, T. G. & Moore, J. H. Avian medullary bone. Nature 172, 504–505 (1953).
Dacke, C. G. et al. Medullary bone and avian calcium regulation. J. Exp. Biol. 184, 63–88 (1993).
Yamamoto, T., Nakamura, H., Tsuji, T. & Hirata, A. Ultracytochemical study of medullary bone calcification in estrogen injected male Japanese quail. Anat. Rec. 264, 25–31 (2001).
Schweitzer, M. H., Elsey, R. M., Dacke, C. G., Horner, J. R. & Lamm, E.-T. Do egg-laying crocodilian (Alligator mississippiensis) archosaurs form medullary bone? Bone 40, 1152–1158, https://doi.org/10.1016/j.bone.2006.10.029 (2007).
Schweitzer, M. H., Wittmeyer, J. L. & Horner, J. R. Gender-specific reproductive tissue in ratites and Tyrannosaurus rex. Science 308, 1456–1460, https://doi.org/10.1126/science.1112158 (2005).
Ostrom, J. H. Archaeopteryx and the origin of birds. Biol. J. Linn. Soc. 8, 91–182 (1976).
Ostrom, J. H. in Problèmes Actuels de Paléontologie (Évolution des Vertébrés) Vol. 218 Colloque International C.N.R.S. (Lehman, J. P. ed) 519-532 (Centre National de la Recherche Scientifique, Paris, France, 1975).
Lee, A. H. & Werning, S. Sexual maturity in growing dinosaurs does not fit reptilian growth models. Proc. Natl Acad. Sci. USA 105, 582–587 (2008).
Hübner, T. R. Bone histology in Dysalotosaurus lettowvorbecki (Ornithischia: Iguanodontia)—variation, growth, and implications. PLoS ONE 7, e29958 (2012).
Tremaine, K., Woodward Ballard, H. & Horner, J. R. in Society of Vertebrate Paleontology 240 (J. Vertebrate Paleont. Berlin, 2014).
Cerda, I. A. & Pol, D. Evidence for gender-specific reproductive tissue in a basal sauropodomorph dinosaur from the Late Triassic of Argentina. Ameghiniana 50, 11–12R (2013).
Chinsamy, A., Cerda, I. A. & Powell, J. E. Vascularised endosteal bone tissue in armoured sauropod dinosaurs. Sci. Rep. 6, 1–9 (2016).
Chinsamy, A., Codorniu, L. & Chiappe, L. M. Palaeobiological implications of the bone histology of Pterodaustro guinazui. Anat. Rec. 292, 1462–1477 (2009).
Prondvai, E. & Stein, K. H. W. Medullary bone-like tissue in the mandibular symphyses of a pterosaur suggests non-reproductive significance. Sci. Rep. 4, 1–9 (2014).
Francillon-Viellot, H. et al. in Skeletal Biomineralization: Patterns, Processes and Evolutionary Trends, Volume I (Carter, J. G. ed) 471-530 (Van Nostrand Reinhold, New York, 1990).
Carter, D. R. & Beaupre, G. Skeletal function and form: mechanobiology of skeletal development, aging, and regeneration. (Cambridge University Press, Cambridge, 2001).
Chinsamy, A. & Tumarkin-Deratzian, A. Pathologic bone tissues in a turkey vulture and a nonavian dinosaur: implications for interpreting endosteal bone and radial fibrolamellar bone in fossil dinosaurs. Anat. Rec. 292, 1478–1848 (2009).
Prondvai, E. Medullary bone in fossils: function, evolution and significance in growth curve reconstructions of extinct vertebrates. J. Evol. Biol. 30, 440–460 (2016).
Cerda, I. A., Chinsamy, A. & Pol, D. Unusual endosteally formed bone tissue in a Patagonian basal sauropodomorph dinosaur. Anat. Rec. 297, 1385–1391 (2014).
Schweitzer, M. H., Zheng, W.-X., Zanno, L. E., Werning, S. & Sugiyama, T. Chemistry supports the identification of gender specific reproductive tissue in Tyrannosaurus rex. Sci. Rep. 6, 1–10 (2016).
Canoville, A., Zanno, L. E., Zheng, W.-X. & Schweitzer, M. H. in 5th International Paleontological Congress. 912.
Werning, S. Medullary bone is phylogenetically widespread and its skeletal distribution varies by taxon. J Ornithol 2018, 1–17 (2018).
Lee, A., Dai, X.-X. & Ezell, K. in 5th International Paleontological Congress. Paris, 918.
Pan, Y.-H., Sha, J.-G., Zhou, Z.-H. & Fürsich, F. T. The Jehol Biota: definition and distribution of exceptionally preserved relicts of a continental Early Cretaceous ecosystem.Cretaceous Res. 44, 30–38 (2008).
O’Connor, J. K., Zheng, X.-T., Hu, H., Wang, X.-L. & Zhou, Z.-H. The morphology of Chiappeavis magnapremaxillo (Pengornithidae: Enantiornithes) and a comparison of aerodynamic function in Early Cretaceous avian tail fans. Vertebr. Palasiat. 55, 1–18 (2017).
Hu, H., O’Connor, J. K. & Zhou, Z.-H. A new species of Pengornithidae (Aves: Enantiornithes) from the Lower Cretaceous of China suggests a specialized scansorial habitat previously unknown in early birds. PLoS ONE 10, e0126791 (2015).
Zhou, Z., Clarke, J. & Zhang, F. Insight into diversity, body size and morphological evolution from the largest Early Cretaceous enantiornithine bird.J. Anat. 212, 565–577 (2008).
O’Connor, J. K., Wang, M., Zheng, X.-T., Wang, X.-L. & Zhou, Z.-H. The histology of two female Early Cretaceous birds. Vertebr. Palasiat. 52, 112–128 (2014).
Chinsamy, A., Chiappe, L. M. & Dodson, P. Mesozoic avian bone microstructure: physiological implications. Paleobiology 21, 561–574 (1995).
Baumel, J. J. & Witmer, L. M. in Handbook of Avian Anatomy: Nomina Anatomica Avium, Second Edition Vol. 23 Publications of the Nuttall Ornithological Club (J. J. Baumel et al eds) 45-132 (Nuttall Ornithological Club, Cambridge, MA, 1993).
Hutchinson, J. R. The evolution of femoral osteology and soft tissues on the line to extant birds (Neornithes). Zool. J. Linn. Soc. 131, 169–197 (2001).
Enlow, D. H. Principles of bone remodeling: an account of post-natal growth and remodeling processes in long bones and the mandible. Am. Lect. Anat. 531, 1–131 (1963).
Teitelbaum, S. L. Bone resorption by osteoclasts. Science 289, 1504–1508 (2000).
Ascenzi, A., François, C. & Bocciarelli, D. S. On the bone induced by estrogens in birds. J. Ultrastruct. Res. 8, 491–505 (1963).
Kerschnitzki, M. et al. Rapid alterations of avian medullary bone material during the daily egg-laying cycle. Bone 69, 109–117 (2014).
Chinsamy, A., Chiappe, L. M., Marugán-Lobón, J., Gao, C.-H. & Zhang, F.-J. Gender identification of the Mesozoic bird Confuciusornis sanctus. Nat. Commun. 4, 1–5, https://doi.org/10.1038/ncomms2377 (2013).
Chiappe, L. M., Ji, S., Ji, Q. & Norell, M. A. Anatomy and systematics of the Confuciusornithidae (Theropoda: Aves) from the Late Mesozoic of northeastern China. Bull. Am. Mus. Nat. Hist. 242, 1–89 (1999).
Erickson, G. M., Rogers, K. C., Varricchio, D. J., Norell, M. A. & Xu, X. Growth patterns in brooding dinosaurs reveals the timing of sexual maturity in non-avian dinosaurs and genesis of the avian condition. Biol. Lett. 3, 558–561 (2007).
Gill, F. B. Ornithology, 3rd Edition. (W.H. Freeman and Company, New York, 2007).
Bourdon, E. et al. Bone growth marks reveal protracted growth in New Zealand kiwi (Aves, Apterygidae). Biol. Lett. 5, 1–4 (2009).
Hu, H. & O’Connor, J. K. First species of Enantiornithes from Sihedang elucidates skeletal development in Early Cretaceous enantiornithines. J. Syst. Palaeontol. 15, 909–926 (2017).
Mayr, G. Avian Evolution: The Fossil Record of Birds and Its Paleobiological Significance. (Wiley & Sons, New Jersey, 2016).
Zheng, X.-T. et al. Preservation of ovarian follicles reveals early evolution of avian reproductive behaviour. Nature 495, 507–511 (2013).
O’Connor, J. K., Zheng, X.-T., Wang, X.-L., Wang, Y. & Zhou, Z.-H. Ovarian follicles shed new light on dinosaur reproduction during the transition towards birds. Natl Sci. Rev. 1, 15–17, https://doi.org/10.1093/nsr/nwt012 (2014).
Wang, Y. et al. A new Jehol enantiornithine bird with three- dimensional preservation and ovarian follicles. J. Vertebr. Paleontol. 36, e1054496 (2016).
Erickson, G. M. et al. Was dinosaurian physiology inherited by birds? Reconciling slow growth in Archaeopteryx. PLoS ONE 4, e7390 (2009).
Reid, R. E. H. Bone histology of the Cleveland-Lloyd dinosaurs and of dinosaurs in general, Part I: Introduction: Introduction to bone tissues. Brigh. Young. Univ. Geol. Stud. 41, 25–72 (1996).
We thank S-K. Zhang (IVPP) for making the histological section of the tibiotarsus. This research was supported by the National Natural Science Foundation of China grant number 41688103 (J.O’C., A.M.B., H.H., Z.Z.) and NSF EAR 0207744 (G.M.E. and M.N.).
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Systemic distribution of medullary bone in the avian skeleton: ground truthing criteria for the identification of reproductive tissues in extinct Avemetatarsalia
BMC Evolutionary Biology (2019)
Nature Communications (2019)