Histology-based skeletochronology is a widely used approach to determine the age of an individual, and is based on the assumption that temporal cessations or decelerations of bone growth lead to ...incremental growth marks (GM), reflecting annual cycles. We studied the reliability of histology-based skeletochronology in a variety of extant tetrapods by comparing two different approaches: petrographic ground sections versus stained microtomized sections. Each bone was cut into two corresponding halves at its growth centre in order to apply both approaches to one and the same sample. None of the samples unequivocally revealed the actual age of the specimens, but truly concerning is the fact that the majority of samples even led to conflicting age estimates between the two approaches. Although the microtomized sections tended to yield more GM and thus indicated an older age than the ground sections, the contrary also occurred. Such a pronounced ambiguity in skeletochronological data strongly challenges the value of the respective age determinations for both extant and extinct animals. We conclude that much more research on the fundamental methodological side of skeletochronology-especially regarding the general nature and microscopic recognition of GM-is required.
Armoured, rigid bodied animals, such as Testudines, must self-right should they find themselves in an inverted position. The ability to self-right is an essential biomechanical and physiological ...process that influences survival and ultimately fitness. Traits that enhance righting ability may consequently offer an evolutionary advantage. However, the energetic requirements of self-righting are unknown. Using respirometry and kinematic video analysis, we examined the metabolic cost of self-righting in the terrestrial Mediterranean spur-thighed tortoise and compared this to the metabolic cost of locomotion at a moderate, easily sustainable speed. We found that self-righting is, relatively, metabolically expensive and costs around two times the mass-specific power required to walk. Rapid movements of the limbs and head facilitate successful righting however, combined with the constraints of breathing whilst upside down, contribute a significant metabolic cost. Consequently, in the wild, these animals should favour environments or behaviours where the risk of becoming inverted is reduced.
In a recent report in Current Biology, Xing and colleagues 1 present a small fragment of a vertebrate tail preserved in amber that bears integumentary appendages (DIP-V-15103, Dexu Institute of ...Paleontology, Chaozhou, China; Figure 1). Following several analyses using cutting-edge technology the authors conclude that: the tail belongs to a non-avian theropod dinosaur (non-avialan according to the authors, but non-avian used synonymously here); the dinosaur most likely was a member of the Coelurosauria, possibly even Maniraptora; and, the integumentary appendages are feathers that support a barbule-first evolutionary pattern for feathers. DIP-V-15103 is indeed an intriguing specimen with potential implications for contributing to understanding the evolution of feathers among dinosaurs, which remains a current and undoubtedly controversial topic 2,3. However, I would like to raise several concerns about the available evidence for the phylogenetic hypothesis concerning the placement of DIP-V-15103 as concluded by Xing and colleagues 1, and furthermore discuss the developmental trajectories predicted by them in light of their far-reaching evolutionary implications.
Lambertz raises concerns about the hypothesis that a recently described feathered fossil in amber represents a non-avian dinosaur and questions the evolutionary scenario for feather development as deduced from the available evidence.
Increased organismic complexity in metazoans was achieved via the specialization of certain parts of the body involved in different faculties (structure–function complexes). One of the most basic ...metabolic demands of animals in general is a sufficient supply of all tissues with oxygen. Specialized structures for gas exchange (and transport) consequently evolved many times and in great variety among bilaterians. This review focuses on some of the latest advancements that morphological research has added to our understanding of how the respiratory apparatus of the primarily terrestrial vertebrates (amniotes) works and how it evolved. Two main components of the respiratory apparatus, the lungs as the “exchanger” and the ventilatory apparatus as the “active pump,” are the focus of this paper. Specific questions related to the exchanger concern the structure of the lungs of the first amniotes and the efficiency of structurally simple snake lungs in health and disease, as well as secondary functions of the lungs in heat exchange during the evolution of sauropod dinosaurs. With regard to the active pump, I discuss how the unique ventilatory mechanism of turtles evolved and how understanding the avian ventilatory strategy affects animal welfare issues in the poultry industry.
Various parts of the respiratory system play an important role in temperature control in birds. We create a simplified computational fluid dynamics (CFD) model of heat exchange in the trachea and air ...sacs of the domestic fowl (Gallus domesticus) in order to investigate the boundary conditions for the convective and evaporative cooling in these parts of the respiratory system. The model is based upon published values for respiratory times, pressures and volumes and upon anatomical data for this species, and the calculated heat exchange is compared with experimentally determined values for the domestic fowl and a closely related, wild species. In addition, we studied the trachea histologically to estimate the thickness of the heat transfer barrier and determine the structure and function of moisture-producing glands. In the transient CFD simulation, the airflow in the trachea of a 2-dimensional model is evoked by changing the volume of the simplified air sac. The heat exchange between the respiratory system and the environment is simulated for different ambient temperatures and humidities, and using two different models of evaporation: constant water vapour concentration model and the droplet injection model. According to the histological results, small mucous glands are numerous but discrete serous glands are lacking on the tracheal surface. The amount of water and heat loss in the simulation is comparable with measured respiratory values previously reported. Tracheal temperature control in the avian respiratory system may be used as a model for extinct or rare animals and could have high relevance for explaining how gigantic, long-necked dinosaurs such as sauropoda might have maintained a high metabolic rate.
Life originated in anoxia, but many organisms came to depend upon oxygen for survival, independently evolving diverse respiratory systems for acquiring oxygen from the environment. Ambient oxygen ...tension (PO2) fluctuated through the ages in correlation with biodiversity and body size, enabling organisms to migrate from water to land and air and sometimes in the opposite direction. Habitat expansion compels the use of different gas exchangers, for example, skin, gills, tracheae, lungs, and their intermediate stages, that may coexist within the same species; coexistence may be temporally disjunct (e.g., larval gills vs. adult lungs) or simultaneous (e.g., skin, gills, and lungs in some salamanders). Disparate systems exhibit similar directions of adaptation: toward larger diffusion interfaces, thinner barriers, finer dynamic regulation, and reduced cost of breathing. Efficient respiratory gas exchange, coupled to downstream convective and diffusive resistances, comprise the "oxygen cascade"-step-down of PO2 that balances supply against toxicity. Here, we review the origin of oxygen homeostasis, a primal selection factor for all respiratory systems, which in turn function as gatekeepers of the cascade. Within an organism's lifespan, the respiratory apparatus adapts in various ways to upregulate oxygen uptake in hypoxia and restrict uptake in hyperoxia. In an evolutionary context, certain species also become adapted to environmental conditions or habitual organismic demands. We, therefore, survey the comparative anatomy and physiology of respiratory systems from invertebrates to vertebrates, water to air breathers, and terrestrial to aerial inhabitants. Through the evolutionary directions and variety of gas exchangers, their shared features and individual compromises may be appreciated.
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