Abstract

Simple SummaryInsects breathe with the aid of thin capillary tubes that open out to the exterior of their body as spiracles. These spiracles are often modulated in a rhythmic gas pattern known as the discontinuous gas exchange cycle. During this cycle, spiracles are either firmly shut to allow no gaseous exchange or slightly open/fully open to allow for gaseous exchange. Two explanations are put forward to rationalize this process, namely, the rhythmic pattern is to (1) reduce water loss or (2) facilitate gaseous exchange in environments with high carbon dioxide and low oxygen. Interestingly, certain insects (such as some desert insects) do not use this rhythmic pattern where it would have been most beneficial and logical. Such an observation has led to the questioning of the explanations of the discontinuous gas exchange cycle. Consequently, we attempt to resolve this controversy by conducting a meta-analysis by synthesizing apposite data from across all insects where a discontinuous gas exchange cycle has been reported. A meta-analysis allows for a shift from viewing data through the lens of a single species to an order view. Thus, our goal is to use this holistic view of data to examine the explanations of the discontinuous gas exchange cycle across multiple groups of insects.The earliest description of the discontinuous gas exchange cycle (DGC) in lepidopterous insects supported the hypothesis that the DGC serves to reduce water loss (hygric hypothesis) and facilitate gaseous exchange in hyperoxia/hypoxia (chthonic hypothesis). With technological advances, other insect orders were investigated, and both hypotheses were questioned. Thus, we conducted a meta-analysis to evaluate the merit of both hypotheses. This included 46 insect species in 24 families across nine orders. We also quantified the percent change in metabolic rates per °C change of temperature during the DGC. The DGC reduced water loss (−3.27 ± 0.88; estimate ± 95% confidence limits [95% CI]; p < 0.0001) in insects. However, the DGC does not favor gaseous exchange in hyperoxia (0.21 ± 0.25 [estimate ± 95% CI]; p = 0.12) nor hypoxia, but did favor gaseous exchange in normoxia (0.27 ± 0.26 [estimate ± 95% CI]; p = 0.04). After accounting for variation associated with order, family, and species, a phylogenetic model reflected that metabolic rate exhibited a significant, non-zero increase of 8.13% (± 3.48 95% CI; p < 0.0001) per °C increase in temperature. These data represent the first meta-analytic attempt to resolve the controversies surrounding the merit of adaptive hypotheses in insects.

Highlights

  • IntroductionInsects modulate (Oxygen) O2 and (carbon dioxide) CO2 by a means of internal airfilled tracheae

  • Insects modulate (Oxygen) O2 and CO2 by a means of internal airfilled tracheae

  • The title and abstract for each paper were screened for relevancy and 979 papers were downloaded from Web of Science (670) and PubMed (309)

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Summary

Introduction

Insects modulate (Oxygen) O2 and (carbon dioxide) CO2 by a means of internal airfilled tracheae. Regardless of the organism and the respiratory medium, gaseous exchange is always through either convection (i.e., bulk flow) and/or diffusion (i.e., movement from a higher concentration to a lower concentration region) [4] This is true because while atmospheric pressure at sea level is 760 mmHg (101.33 kPa), the atmospheric volume of O2 (~21%) and CO2 (~0.04%) creates a partial pressure gradient between the atmosphere and an organism’s interior. The partial pressure (PO2) of oxygen and carbon dioxide (PCO2) is 1590 mm Hg (21.28 kPa) and 0.30 mmHg (0.04 kPa), respectively Based on these calculations and the partial pressure difference in insects, it is easy to see why O2 readily diffuses in and CO2 diffuses out of any living system. It is not uncommon to have the same insect employ more than one gas exchange pattern over a period [5]. This begs the question: what advantage could there be to the choice of one pattern and abandonment of another?

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