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Nitrogen and energy requirements of the short-tailed fruit bat (Carollia perspicillata): fruit bats are not nitrogen constrained

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Abstract

Nitrogen (N) and energy (E) requirements were measured in adultCarollia perspicillata which were fed on four experimental diets. Bats ate 1.3–1.8 times their body mass·day-1 and ingested 1339.5–1941.4 kJ·kg-0.75·day-1. Despite a rapid transit time, dry matter digestibility and metabolizable E coeflicient were high (83.3% and 82.4%, respectively), but true N digestibility was low (67.0%). Mass change was not correlated with E intake, indicating that bats adjusted their metabolic rate to maintain constant mass. Bats were able to maintain constant mass with digestible E intake as low as 1168.7 kJ·kg-0.75·day-1 or 58.6 kJ·. Metabolic fecal N and endogenous urinary N losses were 0.87 mg N·g-1 dry matter intake and 172.5 mg N·kg-0.75·day-1, respectively, and bats required 442 mg N·kg-0.75·day-1 (total nitrogen) or 292.8 mg N·kg-0.75·day-1 (truly digestible nitrogen) for N balance. Based on E and N requirements and digestibilities, it was calculated that non-reproductive fruit bats were able to meet their N requirements without resorting to folivory and without over-ingesting energy. It was demonstrated that low metabolic fecal requirements allowed bats to survive on low-N diets.

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Abbreviations

E :

energy

EUN :

endogenous urinary nitrogen

MFN :

metabolic fecal nitrogen

N :

nitrogen

MR :

metabolic rate

DMD :

dry matter digestibility

References

  • Audet D, Thomas DW (1996) Facultative hypothermia as a thermoregulatory strategy in the Phyllostomid bats,Carollia perspicillata andSturnira lilium. J Comp Physiol B in press

  • Beckman Instruments (1991) Chemistry information manual.CR-T-1-3

  • Bosque C, De Parra O (1992) Digestive efficiency and rate of food passage in oilbird nestlings. Condor 94: 557–571

    Google Scholar 

  • Cunningham Someren GK von (1972) Some fruit bats eat leaves. East Afr Nat Hist Soc Bull 2: 24–25

    Google Scholar 

  • Fleming TH (1988) The Short-tailed fruit bat: a study in plantanimal interactions. The University of Chicago Press, Chicago, USA, p 365

    Google Scholar 

  • Foster MS (1978) Total frugivory in tropical passerines: a reappraisal. Trop Ecol 19: 131–154

    CAS  Google Scholar 

  • Gurr MI, Mawson R, Rothwell NJ, Stock MJ (1980) Effects of manipulating dietary protein and E intake on E balance and thermogenesis in the pig. J Nutr 110: 532–542

    CAS  PubMed  Google Scholar 

  • Herbst LH (1986) The role of nitrogen from fruit pulp in the nutrition of the frugivorous batCarollia perspicillata. Biotropica 18: 39–44

    Google Scholar 

  • Howe HF, Estabrook GF (1977) On intraspecific competition for avian disperser in tropical trees. Amer Nat 111: 817–832

    Google Scholar 

  • Howell DJ (1974) Bats and pollen: physiological aspects of the syndrome of chiropterophily. Comp Biochem Physiol 48A: 263–276

    Google Scholar 

  • Jenness R, Studier EH (1976) Lactation and milk. In: Baker, RJ, et al. (eds) Biology of bats of the New World family Phyllostomatidae, part I. Spec Publ Mus Texas Tech Univ, Lubbock, pp 210–218

    Google Scholar 

  • Karasov WH (1982) E assimilation, nitrogen requirement, and diet in free-living antelope ground squirrels,Ammospermophilus leucurus. Physiol Zool 55: 378–392

    Google Scholar 

  • Korine C, Arad Z, Arieli A (1996) Nitrogen and E balance of the fruit-bat,Rousettus aegyptiacus on natural fruit diets. Physiol Zool (in press)

  • Kunz TH, Diaz CA (1995) Folivory in fruit-eating bats, with new evidence fromArtibeus jamaicensis (Chiroptera: Phyllostomidae). Biotropica 27: 106–120

    Google Scholar 

  • Law BS (1992) The maintenance nitrogen requirements of the Queensland Blossom Bat (Syconycteris australis) on a sugar/pollen diet: is nitrogen a limiting resource? Physiol Zool 65: 634–648

    CAS  Google Scholar 

  • Linzell JL (1972) Milk yield, E loss in milk, and mammary gland weight in different species. Dairy Sci Abstr 34: 351–360

    Google Scholar 

  • Lowry JB (1989) Green-leaf fractionation by fruit bats: is this feeding behaviour a unique nutritional strategy for herbivores? Aust Wildl Res 16: 203–206

    Article  Google Scholar 

  • McKey D (1975) The ecology of co-evolved seed dispersal systems. In: Gilbert LE, Raven PH (eds) Coevolution of animals and plants. Univ Texas Press, Austin, pp 159–191

    Google Scholar 

  • Minson DJ, Milford R (1967) The voluntary intake and digestibility of diets containing different proportions of legume and mature Pangola grass (Digitaria decumbens). Aust J Exp Agric Anim Husb 7: 546–551

    Article  Google Scholar 

  • Morrison DW (1980) Efficiency of food utilisation by fruit bats. Oecologia 45: 270–273

    Article  Google Scholar 

  • Morton ES (1973) On the evolutionary advantages and disadvantages of fruit-eating in tropical birds. Am Nat 107: 8–22

    Article  Google Scholar 

  • Mould ED, Robbins CT (1981) Nitrogen metabolism in elk. J Wildl Manage 45: 323–334

    Google Scholar 

  • Ricklefs RE (1976) Growth rates of birds in the humid new world tropics. Ibis 118: 179–207

    Google Scholar 

  • Robbins CT (1993) Wildife feeding and nutrition. Academic Press, San Diego, p 352

    Google Scholar 

  • Rothwell NJ, Stock MJ (1979) A role for brown adipose tissue in diet-induced thermogenesis. Nature 281: 31–35

    Article  CAS  PubMed  Google Scholar 

  • Schwartz CC, Regelin WL, Franzmann AW (1987) Protein digestion in moose. J Wildl Manage 51: 352–357

    Google Scholar 

  • Smith AP, Green SW (1987) Nitrogen requirements of the sugar glider (Petaurus breviceps), an omnivorous marsupial, on a honey-pollen diet. Physiol Zool 60: 82–92

    CAS  Google Scholar 

  • Smuts DB (1935) The relation between the basal metabolism and the endogenous nitrogen metabolism, with particular reference to the estimation of the maintenance requirement of protein. J Nutr 9: 403–433

    CAS  Google Scholar 

  • Snow DW (1962) The natural history of the Oilbird,Steatornis caripensis, in Trinidad, W.I. Part II. Population, breeding ecology, and food. Zoologica (NY) 47: 199–221

    Google Scholar 

  • Snow DW (1971) Evolutionary aspects of fruit-eating by birds. Ibis 113: 194–202

    Google Scholar 

  • Snow DW (1976) The web of life. Quadrangle, New York

    Google Scholar 

  • Snow DW (1981) Tropical frugivorous birds and their food plants: a world survey. Biotropica 13: 1–14

    Google Scholar 

  • Steller DC (1986) The dietary E and nitrogen requirements of the Grey-Headed Flying Fox,Pteropus poliocephalus (Temminck) (Megachiroptera). Aust J Zool 34: 339–349

    Article  Google Scholar 

  • Tedman RA, Hall LS (1985) The morphology of the gastrointestinal tract and food transit time in the fruit batsPteropus alecto andP. poliocephalus (Megachiroptera). Aust J Zool 33: 625–640

    Article  Google Scholar 

  • Thomas DW (1984) Fruit intake and energy budgets of frugivorous bats. Physiol Zool 57: 457–467

    Google Scholar 

  • Thomas DW, Marshall AG (1984) Reproduction and growth in three species of West African fruit bats. J Zool (Lond) 202: 265–281

    Google Scholar 

  • Thomas DW, Bosque C, Arends A (1993) Development of thermo-regulation and the energetics of nestling oilbirds (Steatornis caripensis). Physiol Zool 66: 322–348

    Google Scholar 

  • Wolton RJ, Arak PA, Godfray HCJ, Wilson RP (1982) Ecological and behavioural studies of the Megachiroptera of Mount Nimba, Liberia, with notes on the Microchiroptera. Mammalia 46: 419–448

    Google Scholar 

  • Zortea M, Mendes SL (1993) Folivory in the big fruit-eating bat,Artibeus lituratus (Chiroptera, Phyllostomidae) in Eastern Brazil. J Trop Ecol 9: 117–120

    Google Scholar 

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Communicated by L.C. -H. Wang

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Delorme, M., Thomas, D.W. Nitrogen and energy requirements of the short-tailed fruit bat (Carollia perspicillata): fruit bats are not nitrogen constrained. J Comp Physiol B 166, 427–434 (1996). https://doi.org/10.1007/BF02337887

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