Form and metabolic scaling in colonial animals

Journal of Experimental Biology

Volumn 217, Issue 5, 2014, Pages 779-786

  Hartikainen, Hanna ^a,b   Humphries, Stuart ^c   Okamura, Beth ^a,b  

^a SWISS FEDERAL INSTITUTE OF AQUATIC SCIENCE AND TECHNOLOGY   (Switzerland)

^b DEPARTMENT OF LIFE SCIENCES   (United Kingdom)

^c UNIVERSITY OF HULL   (United Kingdom)

Author keywords

Bryozoa; Coloniality; Isometry; Modularity; Phylactolaemata; Respiration rate

Indexed keywords

ANIMAL; BIOLOGICAL MODEL; BREATHING RATE; BRYOZOA; COLONIALITY; ENERGY METABOLISM; GROWTH, DEVELOPMENT AND AGING; HISTOLOGY; ISOMETRY; MODULARITY; PHYLACTOLAEMATA; PHYSIOLOGY; REPRODUCTION; REVIEW; SPECIES DIFFERENCE;

BRYOZOA; COLONIALITY; ISOMETRY; MODULARITY; PHYLACTOLAEMATA; RESPIRATION RATE;

ANIMALS; BRYOZOA; ENERGY METABOLISM; MODELS, BIOLOGICAL; REPRODUCTION; SPECIES SPECIFICITY;

EID: 84896888925     PISSN: 00220949     EISSN: None     Source Type: Journal    
DOI: 10.1242/jeb.093484     Document Type: Review

References (53)

1. Agutter, P. S. and Tuszynski, J. A. (2011). Analytic theories of allometric scaling. J. Exp. Biol. 214, 1055-1062.
2. Barnes, D. K. A. and Peck, L. S. (2005). Extremes of metabolic strategy in Antarctic Bryozoa. Mar. Biol. 147, 979-988.
3. Brown, J. H., Gillooly, J. F., Allen, A. P., Savage, V. M. and West, G. B. (2004). Toward a metabolic theory of ecology. Ecology 85, 1771-1789.
4. Chamberlain, J. and Graus, R. R. (1975). Water flow and hydromechanical adaptations of branches reef corals. Bull. Marine Sci. 25, 112-125.
5. Cheetham, A. H. and Jackson, J. B. C. (1992). Speciation, extinction and the decline of arborescent growth in neogene and quaternary cheilostome Bryozoa of tropical America. In Evolution and Evironment in Tropical America (ed. J. B. C. Jackson, A. F. Budd and A. G. Coates), pp. 205-233. Chicago, IL: The University of Chicago Press.
6. Damuth, J. (1981). Population density and body size in mammals. Nature 290, 699-700.
7. DeLong, J. P. (2011). Energetic inequivalence in eusocial insect colonies. Biol. Lett. 7, 611-614.
8. Duursma, R. A., Mäkelä, A., Reid, D. E. B., Jokela, E. J., Porté, A. J. and Roberts, S. D. (2010). Self-shading affects allometric scaling in trees. Funct. Ecol. 24, 723-730.
9. Eckman, J. E. and Okamura, B. (1998). A model of particle capture by bryozoans in turbulent flow: significance of colony form. Am. Nat. 152, 861-880.
10. Ferguson, N., White, C. R. and Marshall, D. J. (2013). Competition in benthic marine invertebrates: the unrecognized role of exploitative competition for oxygen. Ecology 94, 126-135.
11. Glazier, D. S. (2010). A unifying explanation for diverse metabolic scaling in animals and plants. Biol. Rev. Camb. Philos. Soc. 85, 111-138.
12. Grünbaum, D. (1995). A model of feeding currents in encrusting bryozoans shows interference between zooids within a colony. J. Theor. Biol. 174, 411-425.
13. Hartikainen, H., Johnes, P., Moncrieff, C. and Okamura, B. (2009). Bryozoan populations reflect nutrient enrichment and productivity gradients in rivers. Freshw. Biol. 54, 2320-2334.
14. Hartikainen, H., Fontes, I. and Okamura, B. (2013). Parasitism and phenotypic change in colonial hosts. Parasitology 140, 1403-1412.
15. Hemmingsen, A. M. (1960). Energy metabolism as related to body size and respiratory surfaces and its evolution. Rep. Steno. Mem. Hosp. Copenhagen 9, 1-110.
16. Hughes, R. N. (1989). A Functional Biology of Clonal Animals. London: Chapman and Hall.
17. Hughes, R. N. (2005). Lessons in modularity: the evolutionary ecology of colonial invertebrates. Scientia Marina 69, 169-179.
18. Hughes, R. N. and Cancino, J. M. (1985). An ecological overview of cloning in Metazoa. In Population Biology and Evolution of Clonal Organisms (ed. J. B. C. Jackson, L. W. Buss and R. E. Cook), pp. 153-186. London: Yale University Press.
19. Hughes, D. J. and Hughes, R. N. (1986). Metabolic implications of modularity: studies on the respiration and growth of Electra pilosa. Philos. Trans. R. Soc. B 313, 23-29.
20. Jackson, J. B. C. (1979). Morphological strategies of sessile animals. In Biology and Systematics of Colonial Organisms (ed. G. P. Larwood and R. B. Rosen), pp. 499-555. London: Academic Press.
21. Jackson, J. B. C. and Coates, A. G. (1986). Life-cycle and evolution of clonal (modular) animals. Philos. Trans. R. Soc. B 313, 7-22.
22. Kearney, M. R. and White, C. R. (2012). Testing metabolic theories. Am. Nat. 180, 546-565.
23. Kim, K. and Lasker, H. R. (1998). Allometry of resource capture in colonial cnidarians and constraints on modular growth. Funct. Ecol. 12, 646-654.
24. Kleiber, M. (1932). Body size and metabolism. Hilgardia 6, 315-352.
25. Kooijman, S. A. L. M. (1986). Energy budgets can explain body size relations. J. Theor. Biol. 121, 269-282.
26. Kooijman, S. A. L. M. (2010). Dynamic Energy Budget Theory for Metabolic Organisation. Cambridge: Cambridge University Press.
27. Koontz, T. L., Petroff, A., West, G. B. and Brown, J. H. (2009). Scaling relations for a functionally two-dimensional plant: Chamaesyce setiloba (Euphorbiaceae). Am. J. Bot. 96, 877-884.
28. Lidgard, S. (1981). Water flow, feeding and colony form in an encrusting cheilostome. In Recent and Fossil Bryozoa (ed. G. P. Larwood and C. Nielsen), pp. 135-142. Fredensborg: Olsen & Olsen.
29. Maino, J. L., Kearney, M. R., Nisbet, R. M. and Kooijman, S. A. (2013). Reconciling theories for metabolic scaling. J. Anim. Ecol. 83, 20-29.
30. McFadden, C. S. (1986). Colony fission increases particle capture rates of a soft coral: advantages of being a small colony. J. Exp. Mar. Biol. Ecol. 103, 1-20.
31. McKinney, F. K. and Jackson, J. B. C. (1989). Bryozoan Evolution. Boston, MA: Unwin Hyman.
32. McKinney, F. K., Listokin, M. R. A. and Phifer, C. D. (1986). Flow and polypide distribution in the cheilostome bryozoan Bugula and their inference in Archimedes. Lethaia 19, 81-93.
33. Miller, R. J. and Etter, R. J. (2008). Shading facilitates sessile invertebrate dominance in the rocky subtidal Gulf of Maine. Ecology 89, 452-462.
34. Mukai, H., Terakado, K. and Reed, C. G. (1997). Bryozoa. In Microscopic Anatomy of Invertebrates: Lophophorates, Entoprocta and Cycliophora, Vol. 13 (ed. F. W. Harrison and R. M. Woollacott), pp. 45-206. New York, NY: Wiley-Liss.
35. Mundy, S. P. (1980). A key to the British and European freshwater bryozoans. Freshwater Biological Association 41, 1-32.
36. Nakaya, F., Saito, Y. and Motokawa, T. (2003). Switching of metabolic-rate scaling between allometry and isometry in colonial ascidians. Proc. R. Soc. B 270, 1105-1113.
37. Niklas, K. J., Cobb, E. D., Niinemets, U., Reich, P. B., Sellin, A., Shipley, B. and Wright, I. J. (2007). 'Diminishing returns' in the scaling of functional leaf traits across and within species groups. Proc. Natl. Acad. Sci. USA 104, 8891-8896.
38. O'Dea, A., Jackson, J. B., Fortunato, H., Smith, J. T., D'Croz, L., Johnson, K. G. and Todd, J. A. (2007). Environmental change preceded Caribbean extinction by 2 million years. Proc. Natl. Acad. Sci. USA 104, 5501-5506.
39. Okamura, B. (1984). The effects of ambient flow velocity, colony size and upstream colonies on the feeding success of Bryozoa. I. Bugula stolonifera, an arborescent species. J. Exp. Mar. Biol. Ecol. 83, 179-193.
40. Okamura, B. (1985). The effects of ambient flow velocity, colony size and upstream colonies on the feeding success of Bryozoa. II. Conopeum reticulum (Linnaeus), an encrusting species. J. Exp. Mar. Biol. Ecol. 89, 69-80.
41. Peck, L. S. and Barnes, D. K. A. (2004). Metabolic flexibility: the key to long-term evolutionary success in Bryozoa? Proc. R. Soc. B 271 Suppl. 3, S18-S21.
42. Price, C. A., Enquist, B. J. and Savage, V. M. (2007). A general model for allometric covariation in botanical form and function. Proc. Natl. Acad. Sci. USA 104, 13204-13209.
43. Riisgard, H. U., Okamura, B. and Funch, P. (2010). Particle capture in ciliary filterfeeding gymnolaemate and phylactolaemate bryozoans-a comparative study. Acta Zool. Stockholm 91, 416-425.
44. Schmidt-Nielsen, K. (1984). Scaling: Why is Animal Size so Important? Cambridge: Cambridge University Press.
45. Sebens, K. P. (1982). Competition for space: growth rate, reproductive output and escape in size. Am. Nat. 120, 189-197.
46. Tops, S., Hartikainen, H. and Okamura, B. (2009). The effects of infection by Tetracapsuloides bryosalmonae (Myxozoa) and temperature on Fredericella sultana (Bryozoa). Int. J. Parasitol. 39, 1003-1010.
47. Toriumi, M. (1951). Taxonomical study of freshwater Bryozoa. I. Fredericella sultana. Sci. Rep. Tohoku Univ ser. 4 19, 167-177.
48. Warton, D. I., Duursma, R. A., Falster, D. S. and Taskinen, S. (2012). smatr 3-an R package for estimation and inference about allometric lines. Methods Ecol. Evol. 3, 257-259.
49. West, G. B., Brown, J. H. and Enquist, B. J. (1997). A general model for the origin of allometric scaling laws in biology. Science 276, 122-126.
50. West, G. B., Brown, J. H. and Enquist, B. J. (1999). A general model for the structure and allometry of plant vascular systems. Nature 400, 664-667.
51. White, C. R., Kearney, M. R., Matthews, P. G. D., Kooijman, S. A. L. M. and Marshall, D. J. (2011). A manipulative test of competing theories for metabolic scaling. Am. Nat. 178, 746-754.
52. Wood, T. S. (1988). Plumatella reticulata sp. nov. in Ohio (Bryozoa: Phylactolaemata). Ohio J. Sci. 88, 101-104.
53. Wood, T. S. and Okamura, B. (2005). A Key to the British and European Freshwater Bryozoans with Ecological Notes. Ambleside, UK: Freshwater Biological Association.