, Volume 50, Issue 3, pp 291–295 | Cite as

Responses to starvation in a mantis, Paratenodera angustipennis (S.)

  • Toshiaki Matsura


Survival period, pattern of decrease in body weight and metabolic rate under starvation conditions were examined to clarify responses to starvation of a predatory insect, the mantis, Paratenodera angustipennis (S.). (i) The average survival period in starved condition was the shortest in the 1st instar larvae (5.4 days) and the longest in the adults (15.0 days for males, 26.7 days for females). (ii) The body weights of the 3rd and the 5th instar larvae decreased almost linearly during fasting period, whereas those of adults decreased greatly during the initial 5 days, and then exhibited little further decline until their death. (iii) The carbon dioxide production by the adult mantids in the dark condition at constant 26°C was measured by the improved Boysen-Jensen's method. There was a linear relationship between the body weight and the metabolic rate per individual on a double logarithmic scale, and the regression coefficient b was 0.806. (iv) The metabolic rate per individual was greatest at satiation, but the rate per unit weight was maximum on the 5th day after satiation when the food had been just digested completely, and both decreased with the progress of starvation. (v) Based on the above mentioned results, properties of P. angustipennis as a predator were discussed.


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  1. Anderson JF (1970) Metabolic rates of spiders. Comp Biochem Physiol 33:51–72Google Scholar
  2. —, (1974) Responses to starvation in the spiders Lycosa lenta Hentz and Flistata hibernalis (Hentz). Ecology 55:576–585Google Scholar
  3. Dunkan A, Klekowski RZ (1975) Paramerters of an energy budget. Methods for Ecological Bioenergetics, Grodzinski et al. (eds), Blackwell Oxford, 97–147Google Scholar
  4. Hamilton AG (1964) The occurence of periodic or continuous discharge of carbon dioxicide by male dessert locust (Schistocerca gregaria Forskal) measured by an infra-red gas analyzer. Proc Royal Soc Ser B 60:373–395Google Scholar
  5. Ikeda T (1974) Nutritional ecology of marine zooplankton. Mem Fac Fish Hokkaido Univ 22:1–97Google Scholar
  6. Inoue T, Matsura T (1975) Mantis — its hunting behavior. Shizen 30(8):48–56 (In Japanese)Google Scholar
  7. Ito Y (1964) Preliminary studies on the respiratory energy loss of a spider, Lycosa pseudoannulata. Res Popul Ecol 6:13–21Google Scholar
  8. —, Murai M (1977) Dobutsu seitaigaku kenkyuho. Kokinshoin, Tokyo (In Japanese)Google Scholar
  9. Ivlev VS (1955) Experimental ecology of fish nutrition. Pishchepromizdat, Moskva. (In Russian)Google Scholar
  10. Matsura T (1979) Mortality rate and factors during the egg stage of a mantid, Paratenodera angustipennis de Saussure. Bull Kyoto Kyoiku Univ Ser B, 55:49–58 (In Japanese with English summary)Google Scholar
  11. —, Inoue T, Hosomi Y (1975) Ecological studies of a mantid, Paratenodera angustipennis de Saussure I. Evaluation of the feeding condition in natural habitat. Res Popul Ecol 17:64–76Google Scholar
  12. Miyashita K (1968) Quantitative feeding biology of Lycosa T-insignita Boes et Str (Araneae: Lycosidae). Bull Nat Inst Agr Sci (Japan), C-No 22:329–344Google Scholar
  13. Mill PJ (1972) Respiration in the invertebrates. Macmillan, LondonGoogle Scholar
  14. Mukerji MK, LeRoux EJ (1969) A quantitative study of food consumption and growth of Podisus maculiventris (Hemiptera: Pentatomidae). Can Ent 101:387–403Google Scholar
  15. Nakamura K (1972) The ingestion in wolf spiders. II. The expression of degree of hunger and amount of ingestion in relation to spiders hunger. Res Popul Ecol 14:82–96Google Scholar
  16. Omori M (1970) Variations of length, weight, respiratory rate and chemical composition of Calanus cristatus in relation to its food and feeding. JH Steele (ed), Marine food chains. Oliver and Boyd, 113–126Google Scholar
  17. Roverts JL (1957) Thermal acclimation of metabolism in the crab Pachygrapsus crassipes Randall. I. The influence of body size, starvation, and moulting. Physiol Zool 30:232–242Google Scholar
  18. Shibazaki A, Ito Y (1969) Respiratory rates of green and black larvae of the armyworm, Leucania separata (Lepidoptera: Noctuidae). Appl Ent Zool 4:100–101Google Scholar
  19. Turnbull AL (1962) Quantitative studies of the food of Linyphia triangularis Clerk (Araneae: Linyphiidae). Can Ent 94:1233–1249Google Scholar
  20. Vernberg FJ (1959) Studies on the physiological variation between tropical and temperature zone fiddler crabs of the genus Uca. II. Oxygen consumption of whole organisms. Biol Bull 117:163–184Google Scholar
  21. Wise DH (1975) Food limitation of the spider Linyphia marginata: Experimental field studies. Ecology 56:637–646Google Scholar
  22. Yamasaki T (1967) The method of transporting live trout. Suisan Kenkyu Sosho 17:1–56 (In Japanese)Google Scholar

Copyright information

© Springer-Verlag 1981

Authors and Affiliations

  • Toshiaki Matsura
    • 1
  1. 1.Department of ZoologyKyoto Kyoiku UniversityKyotoJapan

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