Increase in tracheal investment with beetle size supports hypothesis of oxygen limitation on insect gigantism

Recent studies have suggested that Paleozoic hyperoxia enabled animal gigantism, and the subsequent hypoxia drove a reduction in animal size. This evolutionary hypothesis depends on the argument that gas exchange in many invertebrates and skin-breathing vertebrates becomes compromised at large sizes because of distance effects on diffusion. In contrast to vertebrates, which use respiratory and circulatory systems in series, gas exchange in insects is almost exclusively determined by the tracheal system, providing a particularly suitable model to investigate possible limitations of oxygen delivery on size. In this study, we used synchrotron x-ray phase–contrast imaging to visualize the tracheal system and quantify its dimensions in four species of darkling beetles varying in mass by 3 orders of magnitude. We document that, in striking contrast to the pattern observed in vertebrates, larger insects devote a greater fraction of their body to the respiratory system, as tracheal volume scaled with mass1.29. The trend is greatest in the legs; the cross-sectional area of the trachea penetrating the leg orifice scaled with mass1.02, whereas the cross-sectional area of the leg orifice scaled with mass0.77. These trends suggest the space available for tracheae within the leg may ultimately limit the maximum size of extant beetles. Because the size of the tracheal system can be reduced when oxygen supply is increased, hyperoxia, as occurred during late Carboniferous and early Permian, may have facilitated the evolution of giant insects by allowing limbs to reach larger sizes before the tracheal system became limited by spatial constraints.

[1]  E R Weibel,et al.  Design of the mammalian respiratory system. V. Scaling morphometric pulmonary diffusing capacity to body mass: wild and domestic mammals. , 1981, Respiration physiology.

[2]  Wah-Keat Lee,et al.  Real-time phase-contrast x-ray imaging: a new technique for the study of animal form and function , 2007, BMC Biology.

[3]  P. Miller The supply of oxygen to the active flight muscles of some large beetles. , 1966, The Journal of experimental biology.

[4]  D. Pauly Tropical fishes: patterns and propensities* , 1998 .

[5]  G. R. Ultsch Gas exchange and metabolism in the Sirenidae (Amphibia: Caudata)--I. Oxygen consumption of submerged sirenids as a function of body size and respiratory surface area. , 1974, Comparative biochemistry and physiology. A, Comparative physiology.

[6]  P. Burri,et al.  The postnatal development and growth of the human lung. II. Morphology. , 1987, Respiration physiology.

[7]  J. Harrison,et al.  Ontogenetic effects on aerobic and anaerobic metabolism during jumping in the American locust, Schistocerca americana , 2005, Journal of Experimental Biology.

[8]  B. O. Wolf,et al.  Intraspecific variation in tracheal volume in the American locust, Schistocerca americana, measured by a new inert gas method , 2006, Journal of Experimental Biology.

[9]  J. Kukalová-Peck,et al.  The ecology of Paleozoic terrestrial arthropods: the fossil evidence , 1990 .

[10]  J. Harrison,et al.  Ontogeny of tracheal dimensions and gas exchange capacities in the grasshopper, Schistocerca americana. , 2005, Comparative biochemistry and physiology. Part A, Molecular & integrative physiology.

[11]  R. Rosenfeld Nature , 2009, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

[12]  J. Harrison,et al.  Ontogeny of tracheal system structure: A light and electron‐microscopy study of the metathoracic femur of the American locust, Schistocerca americana , 2004, Journal of morphology.

[13]  Max Kleiber,et al.  The Fire of Life: An Introduction to Animal Energetics , 1975 .

[14]  N. Stork,et al.  An inordinate fondness for beetles , 2000 .

[15]  J. Harrison,et al.  Body size-independent safety margins for gas exchange across grasshopper species , 2007, Journal of Experimental Biology.

[16]  C. R. Taylor,et al.  The concept of symmorphosis: a testable hypothesis of structure-function relationship. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[17]  E. Weibel Stereological Methods. Practical methods for biological morphometry , 1979 .

[18]  Eric Johnson,et al.  Oxygen Regulation of Airway Branching in Drosophila Is Mediated by Branchless FGF , 1999, Cell.

[19]  T. Garland,et al.  Procedures for the Analysis of Comparative Data Using Phylogenetically Independent Contrasts , 1992 .

[20]  W. Tschinkel,et al.  Phenetic and cladistic relationships among tenebrionid beetles (Coleoptera) , 1982 .

[21]  S. Gould ALLOMETRY AND SIZE IN ONTOGENY AND PHYLOGENY , 1966, Biological reviews of the Cambridge Philosophical Society.

[22]  J. Harrison,et al.  Oxygen partial pressure effects on metabolic rate and behavior of tethered flying locusts. , 2005, Journal of insect physiology.

[23]  E. Weibel,et al.  The postnatal growth of the rat lung. I. Morphometry , 1974, The Anatomical record.

[24]  D. Pauly Why squid, though not fish, may be better understood by pretending they are , 1998 .

[25]  T. Garland,et al.  Why Not to Do Two-Species Comparative Studies: Limitations on Inferring Adaptation , 1994, Physiological Zoology.

[26]  M. Palzenberger,et al.  Gill surface area of water-breathing freshwater fish , 1992, Reviews in Fish Biology and Fisheries.

[27]  J. Lighton,et al.  Scaling of insect metabolic rate is inconsistent with the nutrient supply network model , 2007 .

[28]  J. Harrison,et al.  Plastic and evolved responses of larval tracheae and mass to varying atmospheric oxygen content in Drosophila melanogaster , 2004, Journal of Experimental Biology.

[29]  C. Gans,et al.  Implications of the late Palaeozoic oxygen pulse for physiology and evolution , 1995, Nature.

[30]  J. Harrison,et al.  Respiratory changes throughout ontogeny in the tobacco hornworm caterpillar, Manduca sexta , 2005, Journal of Experimental Biology.

[31]  M. Westoby,et al.  Bivariate line‐fitting methods for allometry , 2006, Biological reviews of the Cambridge Philosophical Society.

[32]  S. Perry,et al.  Stereological Determination of Tracheal Volume and Diffusing Capacity of the Tracheal Walls in the Stick Insect Carausius morosus (Phasmatodea, Lonchodidae) , 1999, Physiological and Biochemical Zoology.

[33]  J. Felsenstein Phylogenies and the Comparative Method , 1985, The American Naturalist.

[34]  C. R. Taylor,et al.  Design of the oxygen and substrate pathways. I. Model and strategy to test symmorphosis in a network structure. , 1996, The Journal of experimental biology.

[35]  W. Thurlbeck,et al.  Postnatal growth of the mouse lung. , 1975, Journal of anatomy.

[36]  M. Plohl,et al.  Preliminary phylogeny of Tribolium beetles (Coleoptera: Tenebrionidae) resolved by combined analysis of mitochondrial genes , 2006 .

[37]  R Dudley,et al.  Atmospheric oxygen, giant Paleozoic insects and the evolution of aerial locomotor performance. , 1998, The Journal of experimental biology.