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Dynamics of biparental care in the dampwood termite, Zootermopsis nevadensis (Hagen): response to nitrogen availability

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Studies were conducted on the dampwood termite, Zootermopsis nevadensis, to examine the behavioral roles of the reproductive pair during the nest-founding period and to determine the effect of nitrogen availability on their reproduction and division of labor. Nitrogen has been hypothesized to be an important limiting nutrient for founding pairs. One nitrogenous reserve, uric acid-nitrogen, was examined in reproductives and in nutrient-receiving and nutrient-gathering colony members; it was found in highest amounts in the reproductives (i.e., alates, de-alates, and primary reproductives). Young pairs may use these nitrogenous reserves to increase their chances for reproduction. In support of this hypothesis, founding pairs that were fed a diet supplemented with uric acid-nitrogen had a significantly greater probability of producing at least one offspring than did pairs fed an unsupplemented diet. Females that were fed a nitrogen-poor diet restricted their total activity while their mates sustained a high activity during colony initiation. When fed a nitrogen-rich diet, females collected pulp more often than their mates, while males collected more water, though only in the period prior to egg laying. In all pairs, males transferred proctodeal pellets (food derived from the hindgut intestine) to their mates significantly more often than females to males, and females fed on proctodeal pellets significantly more often than did their mates. The male-female asymmetries in pellet transfer and feeding were not significant in the stage after egg deposition. Once eggs and larvae were present in the nest, a male and female spend an equal percentage of time caring for eggs and feeding larvae. Proctodeal pellets examined in reproductives were found to be rich in proteins. This suggests that in the pre-egg period, the male provides nitrogen-rich substances to the female as a form of paternal investment.

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References

  • Bartl K, Ziegenhorn J (1983) Uric acid: kinetic UV-method. In: Bergmeyer HU (ed) Methods of enzymatic analysis, vol 7. VCH Publishers, Florida, pp 134–139

    Google Scholar 

  • Benemann JR (1973) Nitrogen fixation in termites. Science 181:164–165

    Google Scholar 

  • Bowen BJ, Codd CG, Gwynne DT (1984) The katydid spermatophore (Orthoptera: Tettigoniidae): male nutritional investment and its fate in the mated female. Aust J Zool 32:23–31

    Google Scholar 

  • Breznak JA (1982) Intestinal microbiota of termites and other xylophagous insects. Annu Rev Microbiol 36:323–343

    Google Scholar 

  • Breznak JA (1984) Biochemical aspects of symbiosis between termites and their intestinal microbiota. In: Anderson JM, Rayner ADM, Watson DWH (eds) Invertebrate-microbial interactions. Cambridge University Press, New York, pp 173–204

    Google Scholar 

  • Breznak JA, Switzer JM (1986) Acetate synthesis from H2 plus CO2 by termite gut microbes. Appl Environ Microbiol 56:623–630

    Google Scholar 

  • Breznak JA, Brill WJ, Mertins JW, Coppel HC (1973) Nitrogen fixation in termites. Nature 244:577–580

    Google Scholar 

  • Cook SF, Scott KG (1933) The nutritional requirements of Zootermopsis angusticollis. J Cell Comp Physiol 4:95–111

    Google Scholar 

  • Dadd RH (1985) Nutrition: organisms. In: Kerkut GA, Gilbert LI (eds) Comprehensive insect physiology, biochemistry, and pharmacology, vol 4. Pergamon Press, New York, pp 313–390

    Google Scholar 

  • Dubbs CA, Davis FW, Adams WS (1956) Simple microdetermination of uric acid. J Biol Chem 218:497–504

    Google Scholar 

  • Eickwort GC (1981) Presocial insects. In: Hermann HR (ed) Social insects, vol 2. Academic Press, New York, pp 199–279

    Google Scholar 

  • Emlen ST, Oring LW (1977) Ecology, sexual selection, and the evolution of mating systems. Science 197:215–223

    CAS  PubMed  Google Scholar 

  • Grassé PP, Noirot C (1945) La transmission des flagellés symbiotiques et les aliments des termites. Bull Biol Fr Belg 79:273–292

    Google Scholar 

  • Gwynne DT, Bowen B, Codd C (1984) The function of the katydid spermatophore and its role in fecundity and insemination (Orthoptera: Tettigoniidae). Aust J Zool 32:15–22

    Google Scholar 

  • Heath H (1927) Caste formation in the termite genus Termopsis. J Morphol Physiol 443:387–425

    Google Scholar 

  • Hendee EC (1934) The association of termites and fungi. In: Koifoid CA (ed) Termites and termite control. 2nd edn. University of California Press, Berkeley, pp 105–116

    Google Scholar 

  • Hendee EC (1935) The role of fungi in the diet of the common dampwood termite, Zootermopsis. Hilgardia 9:499–525

    Google Scholar 

  • Howse PE (1968) On the division of labour in the primitive termite Zootermopsis nevadensis (Hagen). Insectes Soc 15:45–50

    Google Scholar 

  • Howse PE (1970) Termites: a study in social behaviour. Hutchinson, London

    Google Scholar 

  • Hungate RE (1939) Experiments of the nutrition of Zootermopsis, III. The anaerobic carbohydrate dissimilation by the intestinal protozoa. Ecology 20:230–244

    Google Scholar 

  • Hungate RE (1940) Nitrogen content of sound and decayed coniferous woods and its relation to loss in weight during decay. Bot Gaz 102:382–392

    Google Scholar 

  • Hungate RE (1941) Experiments on the nitrogen economy of termites. Annu Entomol Soc Am 34:457–489

    Google Scholar 

  • Hungate RE (1955) Mutualistic intestinal protozoa. In: Hutner SH, Lwoff A (eds) Biochemistry and physiology of protozoa. Academic Press, New York, pp 159–199

    Google Scholar 

  • Katzin LI, Kirby H (1939) The relative weights of termites and their protozoa. J Parasitol 25:444–445

    Google Scholar 

  • LaFage JP, Nutting WL (1978) Nutrient dynamics of termites. In: Brian MV (ed) Production ecology of ants and termites. Cambridge University Press, London, pp 165–232

    Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biol Chem 193: 265–275

    CAS  PubMed  Google Scholar 

  • McMahan EA (1969) Feeding relationships and radioisotopes. In: Krishna K, Weesner F (eds) Biology of termites, vol 1. Academic Press, New York, pp 387–406

    Google Scholar 

  • Mullins DE, Cochran DG (1975a) Nitrogen metabolism in the American cockroach. I. An examination of positive nitrogen balance with respect to uric acid stores. Comp Biochem Physiol 50A:489–500

    Google Scholar 

  • Mullins DE, Cochran DG (1975b) Nitrogen metabolism in the American cockroach. I. An examination of negative nitrogen balance with respect to mobilization to uric acid stores. Comp Biochem Physiol 50A:501–510

    Google Scholar 

  • Mullins DE, Keil CB (1980) Paternal investment of urates in cockroaches. Nature (London) 283:567–569

    Google Scholar 

  • Nalepa CA (1984) Colony composition, protozoan transfer and some life history characteristics of the woodroach Cryptocercus punctulatus Scudder (Dictyoptera: Cryptocercidae). Behav Ecol Sociobiol 14:273–279

    Google Scholar 

  • Nalepa CA (1988) Cost of parental care in the woodroach Cryptocercus punctulatus Scudder (Dictyoptera: Cryptocercidae). Behav Ecol Sociobiol 23:135–140

    Google Scholar 

  • Noirot C, Noirot-Timothée C (1969) The digestive system. In: Krishna K, Weesner FM (eds) Biology of termites, vol 1. Academic Press, New York, pp 49–88

    Google Scholar 

  • Nutting WL (1969) Flight and colony foundation. In: Krishna K, Weesner F (eds) Biology of termites, vol 1. Academic Press, New York, pp 233–282

    Google Scholar 

  • Potrikus CJ, Breznak JA (1980a) Uric acid in wood-eating termites. Insect Biochem 10:19–27

    Google Scholar 

  • Potrikus CJ, Breznak JA (1980b) Uric acid-degrading bacteria in guts of termites Reticulitermes flavipes (Kollar). Appl Environ Microbiol 40:117–124.

    Google Scholar 

  • Potrikus CJ, Breznak JA (1980c) Anaerobic degradation of uric acid by gut bacteria of termites. Appl Environ Microbiol 40:125–132

    Google Scholar 

  • Potrikus CJ, Breznak JA (1981) Gut bacteria recycle uric acid nitrogen in termites: a strategy for nutrient conservation. Proc Natl Acad Sci USA 78:4601–4605

    Google Scholar 

  • Rayner ADM, Boddy L (1988) Fungal decomposition of wood: its biology and ecology. J. Wiley, New York

    Google Scholar 

  • Roonwal ML (1970) Termites of the oriental region. In: Krishna K, Weesner F (eds) Biology of termites, vol 2. Academic Press, New York, pp 315–391

    Google Scholar 

  • Schal C, Bell WJ (1982) Ecological correlates of paternal investment of urates in a tropical cockroach. Science 218:170–173

    CAS  PubMed  Google Scholar 

  • Stuart AM (1969) Social behavior and communication. In: Krishna K, Weesner F (eds) Biology of termites, vol 1. Academic Press, New York, pp 193–232

    Google Scholar 

  • Tallamy DW (1984) Insect parental care. BioScience 34:20–24

    Google Scholar 

  • Thornhill R, Alcock J (1983) The evolution of insect mating systems. Harvard University Press, Cambridge

    Google Scholar 

  • Thornhill R, Gwynne DT (1986) The evolution of sexual differences in insects. Am Sci 74:382–389

    Google Scholar 

  • Van Soest PJ (1982) Nutritional ecology of the ruminant: ruminant metabolism, nutritional strategies, the cellulytic fermentation and the chemistry of forages and plant fibers. Cornell University Press, Ithaca, New York

    Google Scholar 

  • van der Westhuisen NC, Hewitt PH, van der Linde TC de K (1985) Physiological changes during colony establishment in the termite Hodotermes mossambicus (Hagen): water balance and energy content. J Insect Physiol 31:435–440

    Google Scholar 

  • Waller DA, LaFage JP (1987) Nutritional ecology of termites. In: Slansky F, Rodriguez JG (eds) Nutritional ecology of insects, mites, and spiders. Wiley, New York, pp 487–532

    Google Scholar 

  • Watson JAL, Nel JJC, Hewitt PH (1972) Behavioural changes in founding pairs of the termite, Hodotemes mossambicus. J Insect Physiol 18:373–387

    Google Scholar 

  • Wilson EO (1975) Sociobiology: The new synthesis. Belknap Press, Cambridge

    Google Scholar 

  • Yamaoka I, Sasabe K, Terada K (1986) A timely infection of intestinal protozoa in the developing hindgut of the termite (Reticulitermes speratus). Zool Sci 3:175–180

    Article  Google Scholar 

  • Zeh DW, Smith RL (1985) Parental investment by terrestrial arthropods. Am Zool 25:785–805

    Google Scholar 

Download references

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Shellman-Reeve, J.S. Dynamics of biparental care in the dampwood termite, Zootermopsis nevadensis (Hagen): response to nitrogen availability. Behav Ecol Sociobiol 26, 389–397 (1990). https://doi.org/10.1007/BF00170895

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