Summary
The allocation of energy to carapace formation, respiration, growth, and reproduction were examined in two parthenogenetic clones ofDaphnia magna (Cladocera) cultured at two levels of food (Chlorella) concentration. Clonal differences in energy allocation were more apparent at high ration (1.5 μg C mL-1) than at low ration (0.3 μg C mL-1). These differences included respiratory and molting costs, and the timing of energy allocation to growth and reproduction. A comparison of active vs. anesthetized animals revealed that the interclonal difference in respiration rate was the result of a difference in activity level. In both clones mass-specific rates of respiration, growth, and brood production all decreased at low vs. high ration levels, whereas mass-specific molt-loss rate increased. Lowered food concentration decreased the relative allocation of energy to growth and reproduction, but increased allocation to maintenance (respiration and carapace formation). These allocation responses to food limitation indicated that for both clones the highest energy priority was carapace formation. However, the relative priority of respiration, growth and reproduction varied with age and clone. In juveniles (instars 1–4) the priority ranking of growth was essentially equal to that of respiration, whereas respiration always had higher priority in adults (instars 5–9). All three possibilities for the relative ranking of growth and reproduction (i.e., growth>reproduction, growth=reproduction, and reproduction>growth), as specified by different models in the literature, were observed depending on age and clone. The energy allocation rules were also shown to vary between other daphniid species. Furthermore, metabolic responses to chronic food limitation may be different from responses to acute food deprivation. In this study, one clone showed a greater decrease in respiration rate as a result of lifetime food limitation than did the other, but the opposite was true when these clones were exposed to 48 h of starvation. These differences in allocation rules and in acute vs. chronic responses may have to be considered when using physiological data to modelDaphnia populations.
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References
ASTM (1980) Standard practice for conducting acute toxicity tests with fishes, macroinvertebrates, and amphibians. American Standards for Testing and Materials, Philadelphia, PA, USA, pp E729–780
Baird DJ, Barber I, Bradley MC, Soares AMVM, Calow P (1989) The long-term maintenance ofDaphnia magna Straus for use in toxicity tests: problems and prospects. In: Lokke H, Tyle H, BroRasmussen F (eds) Proceedings of the First European Conference on Ecotoxicology. Lyngby, Denmark, pp 144–148
Baird DJ, Barber I, Calow P (1990) Clonal variation in general responses ofDaphnia magna Straus to toxic stress. I. Chronic life-history effects. Funct Ecol 4:399–407
Banta AM, Wood TR, Brown LA, Ingle L (1939) Studies on the physiology, genetics, and evolution of some Cladocera. Carnegie Institution Paper 39, Washington, DC, USA
Barber I, Baird DJ, Calow P (1990) Clonal variation in general responses ofDaphnia magna Straus to toxic stress. II. Physiological effects. Funct Ecol 4:409–414
Bell G, Koufopanou V (1986) The cost of reproduction. In: Dawkins R, Ridley M (eds) Oxford Surveys in Evolutionary Biology. Oxford Univ Press, Oxford, pp 83–131
Bohrer RN, Lampert W (1988) Simultaneous measurement of the effect of food concentration on assimilation and respiration inDaphnia magna Straus. Funct Ecol 2:463–471
Bradley MC, Calow P (1988) The genetical composition ofDaphnia magna used for ecotoxicological testing purposes. (Unpublished EC Contract Report CCAM/87/319). Commission of the European Community
Bradley MC, Perrin N, Calow P (1991) Energy allocation in the cladoceranDaphnia magna Straus, under starvation and refeeding. Oecologia 86:414–418
Elliott JM, Davison W (1975) Energy equivalents of oxygen consumption in animal energetics. Oecologia 19:195–201
Evers EG, Kooijman SALM (1989) Feeding, digestion and oxygen consumption inDaphnia magna. A study in energy budgets. Neth J Zool 39:56–78
Gatto M, Matessi C, Slobodkin LB (1989) Physiological profiles and demographic rates in relation to food quantity and predictability: an optimization approach. Evol Ecol 3:1–30
Gebhardt MD, Stearns SC (1988) Reaction norms for developmental time and weight at eclosion inDrosophila mercatorum. J Evol Biol 1:335–354
Glazier DS (1991) Separating the respiration rates of embryos and brooding females ofDaphnia magna: Implications for the cost of brooding and the allometry of metabolic rate. Limnol Oceanogr 36:354–362
Glazier DS (1992) Effects of food, genotype, and maternal size and age on offspring investment inDaphnia magna. Ecology 73
Goulden CD, Henry LL, Tessier AJ (1982) Body size, energy reserves, and competitive ability in three species of Cladocera. Ecology 63:1780–1789
Hallam TG, Lassiter RR, Li J, Suarez LA (1990) Modelling individuals employing an integrated energy response: application toDaphnia. Ecology 71:938–954
Heisey D, Porter KG (1977) The effect of ambient oxygen concentration on filtering and respiration rates ofDaphnia galeata mendotae andDaphnia magna. Limnol Oceanogr 22:839–845
Hirshfield MF (1980) An experimental analysis of reproductive effort and cost in the Japanese MedakaOryzias latipes. Ecology 61:282–292
Ingle L, Wood TR, Banta AM (1973) A study of longevity, growth, reproduction and heart rate inDaphnia longispina as influenced by limitations in quantity of food. J Exp Zool 76:325–352
Koehn RK, Bayne BL (1989) Towards a physiological and genetical understanding of the energetics of the stress response. Biol J Linnean Soc 37:157–171
Kooijman SALM (1986) Population dynamics on basis of budgets. In: Metz JAJ, Dickmann O (eds) The dynamics of physiologically structured populations. Springer-Verlag, Berlin, pp 266–297
Kooijman SALM, van der Hoeven N, van der Werf DC (1989) Population consequences of a physiological model for individuals. Funct Ecol 3:325–336
Lampert W (1986) Response of the respiratory rate ofDaphnia magna to changing food conditions. Oecologia 70:495–501
Lei C-H, Armitage KB (1980) Energy budget ofDaphnia ambigua Scourfield. J Plankton Res 2:261–281
Lynch M (1989) The life history consequences of resource depression inDaphnia pulex. Ecology 70:246–256
Lynch M, Weider LJ, Lampert W (1986) Measurement of the carbon balance inDaphnia. Limnol Oceanogr 31:17–33
Maynard DM (1960) Circulation and heart function. In: Waterman TH (ed) The physiology of crustacea, vol 1. Academic, New York, pp 161–226
McCauley E, Murdoch WW, Nisbet RM (1990a) Growth, reproduction, and mortality ofDaphnia pulex Leydig: life at low food. Funct Ecol 4:505–514
McCauley E, Murdoch WW, Nisbet RM, Gurney WSC (1990b) The physiological ecology ofDaphnia: development of a model of growth and reproduction. Ecology 71:703–715
Obreshkove V, Banta AM (1930) A study of the rate of oxygen consumption in different Cladocera clones derived originally from a single mother. Physiol Zool 3:1–8
Paloheimo JE, Crabtree SJ, Taylor WD (1982) Growth model ofDaphnia. Can J Fish Aquat Sci 39:598–606
Peters RH (1987) Metabolism inDaphnia. In: Peters RH, de Bernardi R (eds)Daphnia. Mem Ist Ital Idrobiol, 45, Pallanza, pp 193–243
Philippova TG, Postnov AL (1988) The effect of food quantity on feeding and metabolic expenditure in Cladocera. Int Revue ges Hydrobiol 73:601–615
Richman S (1958) The transformation of energy byDaphnia pulex. Ecol Monogr 28:273–291
Schindler DW (1968) Feeding, assimilation and respiration rates ofDaphnia magna under various environmental conditions and their relation to production estimates. J Anim Ecol 37:369–385
Sharma PC, Pant MC (1984) An energy budget forSimocephalus vetulus (O.F. Muller) (Crustacea: Cladocera). Hydrobiologia 111:37–42
Sibly RM, Calow P (1986) Physiological ecology of animals. Blackwell, Oxford
Soares AMVM (1989) Clonal variation in life-history traits inDaphnia magna Straus (Crustacea, Cladocera). Implications for ecotoxicology. PhD dissertation, Univ Sheffield, Sheffield, UK
Sokal RR, Rohlf FJ (1981) Biometry. Freeman, San Francisco
Stearns SC (1989) Trade-offs in life-history evolution. Funct Ecol 3:259–268
Stein JR (1973) Handbook of phycological methods, culture methods and growth measurements. Cambridge Univ Press, Cambridge, England
Taylor BE (1985) Effects of food limitation on growth and reproduction ofDaphnia. Arch Hydrobiol Beih Ergebn Limnol 21:285–296
Threlkeld ST (1979) Estimating cladoceran birth rates: the importance of egg mortality and the egg age distribution. Limnol Oceanogr 24:601–612
Tilman D (1988) Plant strategies and the dynamics and structure of plant communities. Princeton Univ Press, Princeton, NJ, USA
Urabe J, Watanabe Y (1990) Influence of food density on respiration rate of two crustacean plankters,Daphnia galeata andBosmina longirostris. Oecologia 82:362–368
Wulff FV (1980) Animal community structure and energy budget calculations of aDaphnia magna (Straus) population in relation to the rock pool environment. Ecol Modelling 11:179–225
Zaffagnini F (1987) Reproduction inDaphnia. In: Peters RH, De Bernardi R (eds)Daphnia. Mem Ist Ital Idrobiol, 45, Pallanza, pp 245–284
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Glazier, D.S., Calow, P. Energy allocation rules inDaphnia magna: clonal and age differences in the effects of food limitation. Oecologia 90, 540–549 (1992). https://doi.org/10.1007/BF01875448
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DOI: https://doi.org/10.1007/BF01875448