Literature DB >> 15936769

Discontinuous carbon dioxide release in the German cockroach, Blattella germanica (Dictyoptera: Blattellidae), and its effect on respiratory transpiration.

Beatrice N Dingha1, Arthur G Appel, Micky D Eubanks.   

Abstract

The discontinuous gas exchange cycle (DGC) was described in the German cockroach, Blattella germanica (L.) (Dictyoptera: Blattellidae) for the first time. Also, the effect of the DGC on water loss was investigated. The CO(2) emission pattern in both insecticide resistant and susceptible B. germanica varied with temperature. At 10, 15, and 20 degrees C the pattern was discontinuous. Cycle frequency increased at 25 and 30 degrees C, and at 35 degrees C the pattern became cyclic. In most DGCs, there was no clear distinction between the closed and flutter phases in both strains thus data for these phases were combined and analyzed as the interburst phase. The probability that B. germanica would breath discontinuously varied with temperature. Most cockroaches (62.8%) displayed DGCs at 10 degrees C, therefore measurement of metabolic rate and water loss was carried out at this temperature. Using repeated measures of analysis of variance, the interburst and burst V(.)(CO(2))(ml h(-1)) were not significantly different between the two strains. The variability in CO(2) emission during the interburst and burst phases over time was not significantly different from cycle to cycle or between strains. Overall metabolic rate during the entire recording was not significantly different between both strains. There was a significant difference in the duration of the interburst and burst phases between the strains. The susceptible strain had significantly longer interburst and burst phase durations during a complete DGC than the resistant strain. The interburst and burst phase durations were 5.01+/-0.19 and 6.21+/-0.13 min, respectively, for the resistant strain, whereas the durations were 7.16+/-0.37 and 6.73+/-0.17 min, respectively, for the susceptible strain. This resulted in a DGC of significantly longer duration (13.89+/-0.44 min) in the susceptible strain compared with the resistant strain (11.23+/-0.26 min). The duration of the interburst phase was significantly different from the open phase duration in the resistant strain such that during a single DGC lasting approximately 11.23 min, 43.5% consisted of the interburst phase while the burst phase made up 56.5% of the cycle. The cuticular permeability at 10 degrees C and 0% RH was 2.26 microg cm(-2) h(-1) mmHg(-1) for the resistant strain and 3.42 microg cm(-2) h(-1) mmHg(-1) for the susceptible strain. In both strains, cuticular transpiration accounted for approximately 95% of total water loss. The significantly longer duration of the interburst phase of the susceptible strain was not important in reducing water loss.

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Year:  2005        PMID: 15936769     DOI: 10.1016/j.jinsphys.2005.03.014

Source DB:  PubMed          Journal:  J Insect Physiol        ISSN: 0022-1910            Impact factor:   2.354


  4 in total

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Authors:  Chengyu Chen; Wei Mu; Yunhe Zhao; Hui Li; Peng Zhang; Qiuhong Wang; Feng Liu
Journal:  J Insect Sci       Date:  2015-07-12       Impact factor: 1.857

Review 2.  Why Do Insects Close Their Spiracles? A Meta-Analytic Evaluation of the Adaptive Hypothesis of Discontinuous Gas Exchange in Insects.

Authors:  Seun O Oladipupo; Alan E Wilson; Xing Ping Hu; Arthur G Appel
Journal:  Insects       Date:  2022-01-22       Impact factor: 2.769

3.  Respiration patterns of resting wasps (Vespula sp.).

Authors:  Helmut Käfer; Helmut Kovac; Anton Stabentheiner
Journal:  J Insect Physiol       Date:  2013-02-09       Impact factor: 2.354

4.  Water Costs of Gas Exchange by a Speckled Cockroach and a Darkling Beetle.

Authors:  Waseem Abbas; Philip C Withers; Theodore A Evans
Journal:  Insects       Date:  2020-09-14       Impact factor: 2.769

  4 in total

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