Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-10T14:24:43.443Z Has data issue: false hasContentIssue false

Effects of DDT on oxygen consumption of Rhodnius prolixus Stål

Published online by Cambridge University Press:  10 July 2009

D. Spiller
Affiliation:
Plant Diseases Division, Department of Scientific & Industrial Research, Auckland, New Zealand

Extract

When fasting fifth-instar larvae of Rhodnius prolixus Stål were poisoned with a lethal dose of DDT, the rate of oxygen consumption increased from the onset of hyperactivity, reached a marked peak shortly after knockdown, and then declined. For some days after the peak the oxygen consumption was markedly in excess of that prior to poisoning with DDT. Eventually, the oxygen consumption fell below the pre-teatment value and continued at this low level for some days, although the insect was then undoubtedly dead and in one case had been bisected. There was no marked discontinuity in the declining phase of oxygen consumption and therefore there is no indication of when death occurred. It is concluded that the time of death in DDT-poisoned larvae of Rhodnius cannot be determined by measurements of oxygen consumption.

The total oxygen consumed from poisoning until death was always less than that consumed in the normal use of all metabolic reserves by the fasting insect, and these experiments do not support the hypothesis that death in DDT poisoning is due to total exhaustion of metabolic reserves. However, it is pointed out that, in Rhodnius, some of the metabolic reserves are contained in the undigested residue of the blood-meal and in the massive endocuticle and that there is no reason to think that either digestion of the remaining blood-meal or resorption of the endocuticle could be speeded up during DDT poisoning. Hence there is a strong possibility that, in DDT-killed Rhodnius, death is brought about by exhaustion of the available reserves.

The peak rate of oxygen consumption during poisoning was greatest in very recently fed larvae and decreased as the interval between moulting and DDT-treatment was increased. This suggests that knockdown occurs when the fuel demands of the DDT-induced activity exceed the rate at which the fuel can be mobilised from the metabolic reserves.

Type
Research Paper
Copyright
Copyright © Cambridge University Press 1966

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Beament, J. W. L. (1958). A paralysing agent in the blood of cockroaches.—J. Insect Physiol. 2 pp. 199214.CrossRefGoogle Scholar
Buck, J. B. (1948). The anatomy and physiology of the light organ in fireflies.—Ann. N.Y. Acad. Sci. 49 pp. 397482.CrossRefGoogle Scholar
Buck, J. B. & Keister, M. L. (1946). The effects of DDT on respiration and water balance in Phormia.—Anat. Rec. 96 suppl. 4 pp. 34.Google ScholarPubMed
Buck, J. B. & Keister, M. L. (1947). Physiological studies on the mechanism of action of DDT in insects.—Biol. Bull. mar. biol. Lab., Wood's Hole 93 pp. 189190.Google ScholarPubMed
Buck, J. B. & Keister, M. L. (1949). Respiration and water loss in the adult blowfly, Phormia regina, and their relation to the physiological action of DDT.—Biol. Bull. mar. biol. Lab., Wood's Hole 97 pp. 6481.CrossRefGoogle Scholar
Buck, J. B. & Keister, M. L. (1953). Cutaneous and tracheal respiration in the Phormia larva.—Biol. Bull. mar. biol. Lab., Wood's Hole 105 pp. 402411.CrossRefGoogle Scholar
Buck, J. B., Keister, M. L. & Posner, I. (1952). Physiological effects of DDT on Phormia larvae.—Ann. ent. Soc. Am. 45 pp. 369384.CrossRefGoogle Scholar
Dixon, M. (1943). Manometrie methods. 2nd edn, 155 pp. Cambridge, Univ. Pr.Google Scholar
Fullmer, O. H. & Hoskins, W. M. (1951). Effects of DDT upon the respiration of susceptible and resistant houseflies.—J. econ. Ent. 44 pp. 858870.CrossRefGoogle Scholar
Gostick, K. G. (1961). The relationship between increased oxygen uptake and locomotor ataxy or death in insecticide-poisoned Alphitobius laevigatus F.Ann. appl. Biol. 49 pp. 4654.CrossRefGoogle Scholar
Harvey, G. T. & Brown, A. W. A. (1951). The effect of insecticides on the rate of oxygen consumption in Blattella.—Can. J. Zool. 29 pp. 4253.CrossRefGoogle Scholar
Heslop, J. P. & Bay, J. W. (1959). The reaction of the cockroach Periplaneta americana L. to bodily stress and DDT.—J. Insect Physiol. 3 pp. 395401.CrossRefGoogle Scholar
Keiding, J. (1954). Experiments with houseflies. Strains of houseflies bred at the Laboratory.—Arsberetn. St. Skadedyrlab. 1951–1958 pp. 2627.Google Scholar
Laug, E. P. (1945). (Unpublished.) Quoted by Buck & Keister, 1949.Google Scholar
Lord, K. A. (1949). The effect of insecticides on the respiration of Oryzaephilus Surinamensis: an attempt to compare the speeds of action of a number of D.D.T. analogues.—Ann. appl. Biol. 36 pp. 113138.CrossRefGoogle Scholar
Ludwig, D. (1946). The effect of DDT on the metabolism of the Japanese beetle, Popillia japonica Newman.—Ann. ent. Soc. Am. 39 pp. 496509.CrossRefGoogle Scholar
Nigam, P. C. & Musgrave, A. J. (1964). Effect of DDT and starvation on the antigenic composition of Sitophilus granarius (L.) (Coleoptera), GG strain, and a comparison with other strains and species, using the Ouchterlony technique.—Can. J. Zool. 42 pp. 10411048.CrossRefGoogle Scholar
Both, A. E., Lindquist, A. W. & Tereiere, L. C. (1953). Effect of temperature and the activity of houseflies on their absorption of DDT.—J. econ. Ent. 46 pp. 127130.Google Scholar
Sacktor, B. (1952). Conference on insecticide resistance and insect physiology.—Publ. natn. Res. Coun., Wash. no. 219, p. 35.Google Scholar
Spiller, D. (1965), Effects of the insecticide DDT on the physiology of an insect, Rhodnius prolixus.–Thesis, Univ. Cambridge.Google Scholar
Wigglesworth, V. B. (1933). The physiology of the cuticle and of ecdysis in Rhodnius prolixus.—Q. J. microsc. Sci. 76 pp 269318.Google Scholar
Wigglesworth, V. B. (1955). The mode of action of DDT.–In Müller, P. Ed. DDT.–Das Insektizid Dichlorodiphenyltrichloroathan und seine Bedeutung. Vol. 1. pp. 91111. Basel, Birkhauser.CrossRefGoogle Scholar
Wigglesworth, V. B. & Gillett, J. D. (1936). The loss of water during ecdysis in Rhodnius prolixus Stål (Hemiptera).—Proc. R. ent. Soc. Land. (A) 11 pp. 104107.Google Scholar
Winteringham, F. P. W. (1962). Action and inaction of insecticides.—Jl R. Soc. Arts 110 pp. 719740.Google Scholar
Winteringham, F. P. W., Hellyer, G. C. & McKay, M. A. (1960). Effects of the insecticides DDT and dieldrin on phosphorus metabolism of the adult housefly Musca domestica L.Biochem. J. 76 pp. 543548.CrossRefGoogle ScholarPubMed
Zwicky, K. & Wigglesworth, V. B. (1956). The course of oxygen consumption during the moulting cycle of Rhodnius prolixus Stål (Hemiptera).—Proc. R. ent. Soc. Lond. (A) 31 pp. 153160.Google Scholar