Cited by 115Physiological and biochemical adaptationsCrustacean biology and ecologyTardigrade Biology and Ecology

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Oxygen limitation and thermal tolerance in two terrestrial arthropod species

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Stevens, Meagan M., Jackson, Sue, Bester, Susan A., Terblanche, John S., Chown, Steven L.·2010·Journal of Experimental Biology

Abstract

SUMMARY: Recent studies of marine invertebrates and fish have suggested that lower and upper critical temperatures (CTmin and CTmax) are coupled by a common mechanism: oxygen and capacity limitation of thermal tolerance (OCLT). Using thermolimit respirometry, we tested the predictions of this theory for terrestrial arthropods by measuring maxima and minima for both critical temperatures and metabolic rate in two arthropods, the isopod Porcellio scaber and the beetle Tenebrio molitor, at 40%, 21%, 10% and 2.5% ambient O2. Critical temperatures were identified as particular points on both activity and traces in four ways. In the first two instances, we identified the inflection points in regressions of absolute difference sum (ADS) residuals calculated for activity (aADS) and (VI), respectively. In the third, we visually identified the lowest point before the post-mortal peak in CO2 release (PMV). Finally, we pinpointed the sudden drop in at death, where fell outside the 95% confidence intervals of the 5 min period immediately preceding the drop-off (CI). Minimum and maximum metabolic rates were determined using CO2 traces, and the temperatures corresponding to these identified as TMetMin and TMetMax. For both species, ambient oxygen concentration did not influence CTmin, minimum metabolic rate, or TMetMin. By contrast, severe hypoxia (2.5% O2) caused a 6.9°C decline in activity-based CTmax for T. molitor and a 10.6°C decline for P. scaber, relative to normoxia (21% O2). The magnitude of this decrease differed between methods used to estimated critical thermal limits, highlighting the need for a standard method to determine these endpoints during thermolimit respirometry. Maximum metabolic rate also declined with decreasing ambient oxygen in both species. The combination of increasing metabolic rate and oxygen limitation affected upper thermal limits in these arthropods only in severe hypoxia (2.5% O2). In both species, CTmin and CTmax responded differently to oxygen limitation, suggesting that this is not a common mechanism coupling upper and lower limits in terrestrial arthropods.

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Research works printed but not linked: 42

  1. Bridges, 1997, Ecophysiological adaptations to dry thermal environments measured in two unrestrained Namibian scorpions, Parabuthus villosus (Buthidae) and Opisthophthalmus flavescens (Scorpionidae), Physiol. Zool., 70, 244, 10.1086/639587 · DOI
  2. Chapman, 1998, The Insects: Structure and Function, 10.1017/CBO9780511818202 · DOI
  3. Chown, 2001, Physiological variation in insects: hierarchical levels and implications, J. Insect Physiol., 47, 649, 10.1016/S0022-1910(00)00163-3 · DOI
  4. Chown, 2004, Insect Physiological Ecology: Mechanisms and Patterns, 10.1093/acprof:oso/9780198515494.001.0001 · DOI
  5. Chown, 2007, Physiological diversity in insects: ecological and evolutionary contexts, Adv. Insect Physiol., 33, 50, 10.1016/S0065-2806(06)33002-0 · DOI
  6. Chown, 2009, Phenotypic variance, plasticity and heritability estimates of critical thermal limits depend on methodological context, Funct. Ecol., 23, 133, 10.1111/j.1365-2435.2008.01481.x · DOI
  7. Cloudsley-Thompson, 1975, Adaptations of Arthropoda to arid environments, Annu. Rev. Entomol., 20, 261, 10.1146/annurev.en.20.010175.001401 · DOI
  8. Esch, 1988, The effects of temperature on flight muscle potentials in honeybees and Cuculiinid winter moths, J. Exp. Biol., 135, 109, 10.1242/jeb.135.1.109 · DOI
  9. Frederich, 2000, Oxygen limitation of thermal tolerance defined by cardiac and ventilatory performance in spider crab, Maja squinado, Am. J. Physiol., 279, R1531
  10. Goller, 1990, Comparative study of chill-coma temperatures and muscle potentials in insect flight muscles, J. Exp. Biol., 150, 221, 10.1242/jeb.150.1.221 · DOI
  11. Gray, 2006, Evidence from mosquitoes suggests that cyclic gas exchange and discontinuous gas exchange are two manifestations of a single respiratory pattern, J. Exp. Biol., 209, 1603, 10.1242/jeb.02181 · DOI
  12. Hazell, 2008, A method for the rapid measurement of thermal tolerance traits in studies of small insects, Physiol. Entomol., 33, 389, 10.1111/j.1365-3032.2008.00637.x · DOI
  13. Hoback, 1996, Lethal limits and sublethal effects of hypoxia on the amphipod Gammarus pseudolimnaeus, J. North American Benthological Society, 15, 117, 10.2307/1467437 · DOI
  14. Hochachka, 2002, Biochemical Adaptation: Mechanisms and Processes in Physiological Evolution, 10.1093/oso/9780195117028.001.0001 · DOI
  15. Hochberg, 1990, More powerful procedures for multiple significance testing, Stat. Med., 9, 811, 10.1002/sim.4780090710 · DOI · Paper page
  16. Hoffmann, 2003, Adaptation of Drosophila to temperature extremes: bringing together quantitative and molecular approaches, J. Therm. Biol., 28, 175, 10.1016/S0306-4565(02)00057-8 · DOI
  17. Hoffmann, 2005, Relative importance of plastic vs genetic factors in adaptive differentiation: geographical variation for stress resistance in Drosophila melanogaster from eastern Australia, Funct. Ecol., 19, 222, 10.1111/j.1365-2435.2005.00959.x · DOI
  18. Hopkin, 1991, A key to the woodlice of Britain and Ireland, Field Studies, 7, 599
  19. Hosler, 2000, Flight muscle resting potential and species-specific differences in chill-coma, J. Insect Physiol., 46, 621, 10.1016/S0022-1910(99)00148-1 · DOI
  20. Klok, 1997, Critical thermal limits, temperature tolerance and water balance of a Sub-Antarctic caterpillar, Pringleophaga marioni (Lepidoptera: Tineidae), J. Insect Physiol., 43, 685, 10.1016/S0022-1910(97)00001-2 · DOI
  21. Klok, 2004, Upper thermal tolerance and oxygen limitation in terrestrial arthropods, J. Exp. Biol., 207, 2361, 10.1242/jeb.01023 · DOI · Paper page
  22. Kovac, 2007, Respiration of resting honeybees, J. Insect Physiol., 53, 1250, 10.1016/j.jinsphys.2007.06.019 · DOI
  23. Lighton, 2007, Hot hypoxic flies: whole-organism interactions between hypoxic and thermal stressors in Drosophila melanogaster, J. Therm. Biol., 32, 134, 10.1016/j.jtherbio.2007.01.009 · DOI
  24. Lighton, 2004, Thermolimit respirometry: an objective assessment of critical thermal maxima in two sympatric desert harvester ants, Pogonomyrmex rugosus and P. californicus, J. Exp. Biol., 207, 1903, 10.1242/jeb.00970 · DOI
  25. Loudon, 1989, Tracheal hypertrophy in mealworms: design and plasticity in oxygen supply systems, J. Exp. Biol., 147, 217, 10.1242/jeb.147.1.217 · DOI
  26. Makarieva, 2006, Size- and temperature-independence of minimum life-supporting metabolic rates, Funct. Ecol., 20, 83, 10.1111/j.1365-2435.2006.01070.x · DOI
  27. Mark, 2002, Oxygen-limited thermal tolerance in Antarctic fish investigated by MRI and 31P-MRS, Am. J. Physiol. Reg. Int. Physiol., 283, R1254, 10.1152/ajpregu.00167.2002 · DOI
  28. Mellanby, 1939, Low temperature and insect activity, Proc. R. Soc. Lond. B, 127, 473, 10.1098/rspb.1939.0035 · DOI
  29. Pörtner, 2001, Climate change and temperature-dependent biogeography: oxygen limitation of thermal tolerance in animals, Naturwissenschaften, 88, 137, 10.1007/s001140100216 · DOI
  30. Pörtner, 2002, Climate variations and the physiological basis of temperature dependent biogeography: systemic to molecular hierarchy of thermal tolerance in animals, Comp. Biochem. Physiol., 132A, 739, 10.1016/S1095-6433(02)00045-4 · DOI
  31. Pörtner, 2007, Climate change affects marine fishes through the oxygen limitation of thermal tolerance, Science, 315, 95, 10.1126/science.1135471 · DOI · Paper page
  32. Pörtner, 1999, Mitochondrial function and critical temperature in the Antarctic bivalve, Laternula elliptica, Comp. Biochem. Physiol., 124A, 179, 10.1016/S1095-6433(99)00105-1 · DOI
  33. Pörtner, 2006, Trade-offs in thermal adaptation: the need for a molecular to ecological integration, Physiol. Biochem. Zool., 79, 295, 10.1086/499986 · DOI
  34. Prosser, 1973, Oxygen: respiration and metabolism, 165
  35. Sinclair, 2004, Metabolism of the sub-Antarctic caterpillar Pringleophaga marioni during cooling, freezing and thawing, J. Exp. Biol., 207, 1287, 10.1242/jeb.00880 · DOI
  36. Storey, 2004, Oxygen limitation and metabolic rate depression, 10.1002/047167558X · DOI
  37. Terblanche, 2007, Critical thermal limits depend on methodological context, Proc. R. Soc. Lond. B, 274, 2935
  38. White, 2006, Respirometry: anhydrous Drierite equilibrates with carbon dioxide and increases washout times, Physiol. Biochem. Zool., 79, 977, 10.1086/505994 · DOI
  39. Wigglesworth, 1972, The Principles of Insect Physiology, 10.1007/978-94-009-5973-6 · DOI
  40. Withers, 2001, Design, calibration and calculation for flow-through respirometry systems, Aust. J. Zool., 49, 445, 10.1071/ZO00057 · DOI
  41. Woods, 2004, Temperature-dependent oxygen limitation in insect eggs, J. Exp. Biol., 207, 2267, 10.1242/jeb.00991 · DOI
  42. Wright, 2006, Respiratory physiology of Oniscidea: aerobic capacity and the significance of pleopodal lungs, Comp. Biochem. Physiol., 145A, 235, 10.1016/j.cbpa.2006.06.020 · DOI

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Metadata

Authors
Stevens, M. M., Jackson, S., Bester, S. A., Terblanche, J. S., & Chown, S. L.
Affiliations
Stellenbosch University (ZA)
Corresponding author
Jackson, Sue
Venue
Journal of Experimental Biology
Published
2010-07-01
Volume
213
Issue
13
Pages
2209-2218
ISSN
  • 0022-0949 (ISSN-L)
  • 1477-9145
OpenAlex
W2157683714
Cited by
115
References
2
Citations by year
2026: 4 · 2025: 6 · 2024: 3 · 2023: 5 · 2022: 3 · 2021: 9 · 2020: 7 · 2019: 7 · 2018: 8 · 2017: 6 · 2016: 9 · 2015: 12 · 2014: 10 · 2013: 7 · 2012: 12
FWCI
7.50
Type
journal article
Language
en
Open access
Locations
  • Journal of Experimental Biology (publishedVersion)
  • PubMed (publishedVersion)
  • SUNScholar (Stellenbosch University) (submittedVersion)
Funders
National Research Foundation
Topics
  • Physical Sciences › Environmental Science › Ecology › Physiological and biochemical adaptations
  • Physical Sciences › Environmental Science › Ecology › Crustacean biology and ecology
  • Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Tardigrade Biology and Ecology
Keywords
oxygen limitation, heat tolerance, critical thermal limits, hypoxia, Porcellio scaber, Tenebrio molitor, terrestrial arthropods, metabolic rate, upper critical temperature, lower critical temperature
MeSH terms
Animals, Oxygen, Temperature, Tenebrio, Isopoda

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