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Adaptations for the maintenance of water balance by three species of Antarctic mites

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Abstract

Three species of Antarctic mites, Alaskozetes antarcticus, Hydrogamasellus antarcticus and Rhagidia gerlachei, are abundant in the vicinity of Palmer Station, Antarctica. No single mechanism for reducing water stress was shared by all three species. A. antarcticus and R. gerlachei (both ca. 200 μg) are over twice as large as H. antarcticus (ca. 90 μg), but all had similar body water content (67%) and tolerated a loss of up to 35% of their body water before succumbing to dehydration. All imbibed free water and had the capacity to reduce water loss behaviorally by forming clusters. Alaskozetes antarcticus was distinct in that it relied heavily on water conservation (xerophilic classification) that was largely achieved by its thick cuticular armor, a feature shared by all members of this suborder (Oribatida), and abundant cuticular hydrocarbons. In comparison to the other two species, A. antarcticus was coated with 2–3× the amount of cuticular hydrocarbons, had a 20-fold reduction in net transpiration rate, and had a critical transition temperature (CTT) that indicates a pronounced suppression in activation energy (E a) at temperatures below 25°C. In contrast, H. antarcticus and R. gerlachei lack a CTT, have lower amounts of cuticular hydrocarbons and have low E as and high net transpiration rates, classifying them as hydrophilic. Only H. antarcticus was capable of utilizing water vapor to replenish its water stores, but it could do so only at relative humidities close to saturation (95–98 %RH). Thus, H. antarcticus and R. gerlachei require wet habitats and low temperature to counter water loss, and replace lost water behaviorally through predation. Compared to mites from the temperate zone, all three Antarctic species had a lower water content, a feature that commonly enhances cold tolerance.

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References

  • Arlian LG, Wharton GW (1974) Kinetics of active and passive water exchange between the air and a mite, Dermatophagoides farinae. J Insect Physiol 20:1063–1077

    Article  PubMed  CAS  Google Scholar 

  • Arlian LG, Ekstrand IA (1975) Water balance in Drosophilia pseudoobscura, and its ecological implications. Ann Entomol Soc Am 68:827–832

    Google Scholar 

  • Arlian LG, Veselica MM (1979) Water balance in insects and mites. Comp Biochem Physiol A 64:191–200

    Article  Google Scholar 

  • Bayley M, Holmstrup M (1999) Water vapour absorption in arthropods by accumulation of myoinositol and glucose. Science 285:1909–1911

    Article  PubMed  CAS  Google Scholar 

  • Benoit JB, Denlinger DL (2007) Suppression of water loss during adult diapause in the northern house mosquito, Culex pipiens. J Exp Biol 210:217–226

    Article  PubMed  Google Scholar 

  • Benoit JB, Yoder JA, Rellinger EJ, Ark JT, Keeney GD (2005) Prolonged maintenance of water balance by adult female of the American spider beetle, Mezium affine Boieldieu, in the absence of food and water resources. J Insect Physiol 51:565–573

    Article  PubMed  CAS  Google Scholar 

  • Benoit JB, Yoder JB, Lopez-Martinez G, Elnitsky MA, Lee Jr RE, Denlinger DL (2007) Habitat requirements of the seabird tick, Ixodes uriae (Acari: Ixodidae), from the Antarctic Peninsula in relation to water balance characteristics of eggs, nonfed and engorged stages. J Comp Physiol B 177:205–215

    Article  PubMed  CAS  Google Scholar 

  • Block W, Convey P (1995) The biology, life cycle and ecophysiology of the Antarctic mite, Alaskozetes antarcticus. J Zool 236:431–449

    Google Scholar 

  • Block W, Young SR, Conradi-Larsen EM, Sømme L (1978) Cold tolerance of two Antarctic terrestrial arthropods. Cell Mol Life Sci 34:1166–1167

    Google Scholar 

  • Block W (1981) Terrestrial arthropods and low temperatures. Cryobiology 18:436–444

    Article  PubMed  CAS  Google Scholar 

  • Block W (1977) Oxygen consumption of the terrestrial mite Alaskozetes antarcticus (Acari: Cryptostigmata). J Exp Biol 68:69–87

    Google Scholar 

  • Cannon RJC (1986) Effects of contrasting relative humidities on the cold tolerance of an Antarctic mite. J Insect Physiol 32:523–534

    Article  Google Scholar 

  • Gaede K (1992) On the water balance of Phytoseiulus persimilis A.-H. and its ecological significance. Exp Appl Acarol 15:181–198

    Article  Google Scholar 

  • Gibbs AG (2002) Lipid melting and cuticular permeability: new insights into an old problem. J Insect Physiol 48:391–400

    Article  PubMed  CAS  Google Scholar 

  • Glass EV, Yoder JA, Needham GR (1997) Clustering reduces water loss by adult American house dust mites Dermatophagoides farinae (Acari: Pryoglyphidae). Exp Appl Acarol 22:31–37

    Article  Google Scholar 

  • Gressitt JL (1967a) Notes on arthropod populations in the Antarctic Peninsula-South Shetland Islands-South Orkney Islands area. In: Gressitt JL (ed) Entomology of Antarctica. Horn-Shafer Co., Baltimore, pp 373–392

    Google Scholar 

  • Gressitt JL (1967b) Introduction to entomology in Antarctica. In: Gressitt JL (ed) Entomology of Antarctica. Horn-Shafer Co., Baltimore, pp 2–34

    Google Scholar 

  • Hadley NF (1994) Water relations of terrestrial arthropods. Academic, New York

    Google Scholar 

  • Hayward SAL, Bale JS, Worland MR, Convey P (2001) Influence of temperature -on the hygropreferences of the Collembolan, Cryptopygus antarcticus, and the mite, Alaskozetes antarcticus from the maritime Antarctic. J Insect Physiol 47:11–18

    Article  PubMed  CAS  Google Scholar 

  • Hayward SAL, Worland MR, Convey P, Bale JS (2003) Temperature preferences of the mite, Alaskozetes antarcticus, and the collembolan, Cryptopygus antarcticus from the maritime Antarctic. Physiol Entomol 28:114–121

    Article  Google Scholar 

  • Peckham V (1967) Studies of the mite Alaskozetes antarcticus (Michael). Antarct J US 2:196–197

    Google Scholar 

  • Rourke BC, Gibbs AG (1999) Effects of lipid phase transitions on cuticular permeability: model membrane and in situ studies. J Exp Biol 202:3255–3262

    PubMed  Google Scholar 

  • Seathaler H, Knülle W, Devine TL (1979) Water vapor intake and body water (3HOH) clearance in the housemite Glycyphagus domesticus. Acarologia 21:440–450

    Google Scholar 

  • Shimada K, Pan C, Ohyama Y (1992) Variation in summer cold hardiness of the Antarctic oribatid mite Alaskozetes antarcticus from contrasting habitats on King George Island. Polar Biol 12:701–706

    Article  Google Scholar 

  • Sokal RR, Rohlf FJ (1995) Biometry: the principles and practice of statistics in biological research. Freeman, San Francisco

    Google Scholar 

  • Strong J (1967) Ecology of terrestrial arthropods at Palmer Station, Antarctic Peninsula. In: Gressitt JL (ed) Entomology of Antarctica. Horn-Shafer Co., Baltimore, pp 357–372

    Google Scholar 

  • Toolson EC (1978) Diffusion of water through the arthropod cuticle: thermodynamic consideration of the transition phenomenon. J Therm Biol 3:69–73

    Article  Google Scholar 

  • Wharton GW (1985) Water balance of insects. In: Kerkut GA, Gilbert LI (eds) Comprehensive insect physiology, biochemistry, and physiology, vol 4. Pergamon Press, Oxford, pp 565–603

    Google Scholar 

  • Wharton G, Kanungo K (1962) Some effects of temperature and relative humidity on water balance in females of the spring rat mite, Echinolaelaps echidnina (Acarina: Laelaptidae). Ann Entomol Soc Amer 55:483–492

    Google Scholar 

  • Winston PW, Bates DS (1960) Saturated salt solutions for the control of humidity in biological research. Ecology 41:232–237

    Article  Google Scholar 

  • Worland MR, Block W (1986) Survival and water loss in some Antarctic arthropods. J Insect Physiol 32:579–584

    Article  Google Scholar 

  • Worland MR, Block W (2003) Desiccation at sub-zero temperatures in polar terrestrial arthropods. J Insect Physiol 49:193–203

    Article  PubMed  CAS  Google Scholar 

  • Yoder JA (1998) A comparison of the water balance characteristics of Typhlodromus occidentalis and Amblyseius finlandicus mites (Acari: Phytoseiidae), and evidence for the site of water vapor uptake. Exp Appl Acarol 22:279–286

    Article  Google Scholar 

  • Yoder JA, Barcelona JC (1995) Food and water resources used by the Madagacar hissing-cockroach, Gromphadorholaelaps schaeferi. Exp Appl Acarol 19:259–273

    Article  Google Scholar 

  • Yoder JA, Houck MA (2001) Xeric survival without drinking by hypopodes of Hemisarcoptes cooremani (Acari: Hemisarcoptidae). Int J Acarology 27:59–62

    Google Scholar 

  • Yoder JA, Klompen H (2001) Water relations of Julolaelaps sp. (Mesostigmata: Iphiopsididae) with inferences on its biology. Int J Acarology 27:55–58

    Google Scholar 

  • Yoder JA, Sammataro D, Peterson JA, Needham GR, Bruce WA (1999) Water requirements of adultfemales of the honey bee parasitic mite, Varroa jacobsoni (Acari: Varroidae) and implications for control. Int J Acarol 25:329–335

    Article  Google Scholar 

  • Yoder JA, Benoit JB, Rellinger EJ, Ark JT (2005a) Letter to the editor: critical transition temperature and activation energy with implications for arthropod cuticular permeability. J Insect Physiol 51:1063–1065

    Article  PubMed  CAS  Google Scholar 

  • Yoder JA, Benoit JB, Ark JT, Rellinger EJ (2005b) Temperature-induced alteration of cuticular lipids are not required for transition phenomenon in ticks. Int J Acarology 31:175–181

    Google Scholar 

  • Yoder JA, Ark JT, Benoit JB, Rellinger EJ, Gribbins KM (2006) Water balance components in adults of terrestrial red mite Balaustium sp. (Acarina: Erythraeidae). Ann Entomol Soc Am 99:560–566

    Article  Google Scholar 

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Acknowledgments

We thank Dr. J. H. Klompen, Ohio State University, for identification of the mites and the staff at the Palmer Research Station for their assistance. This research was funded by NSF grants OPP-0337656 and OPP-0413786.

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Authors and Affiliations

  1. Department of Entomology, The Ohio State University, 318 W. 12th Ave, Columbus, OH, 43210, USA

    J. B. Benoit, G. Lopez-Martinez & D. L. Denlinger

  2. Department of Biology, Wittenberg University, Springfield, OH, 45501, USA

    J. A. Yoder

  3. Department of Zoology, Miami University, Oxford, OH, 45056, USA

    M. A. Elnitsky & R. E. Lee Jr.

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  1. J. B. Benoit
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  2. J. A. Yoder
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  3. G. Lopez-Martinez
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  4. M. A. Elnitsky
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  5. R. E. Lee Jr.
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  6. D. L. Denlinger
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Correspondence to J. B. Benoit.

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Benoit, J.B., Yoder, J.A., Lopez-Martinez, G. et al. Adaptations for the maintenance of water balance by three species of Antarctic mites. Polar Biol 31, 539–547 (2008). https://doi.org/10.1007/s00300-007-0385-9

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  • DOI: https://doi.org/10.1007/s00300-007-0385-9

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