Skip to main content

Advertisement

Log in

Metabolism and water loss are not related to environmental heterogeneity in two mygalomorph spiders

  • Original Paper
  • Published:
The Science of Nature Aims and scope Submit manuscript

Abstract

Regulation of energy and water balance are primary components of homeostasis in all organisms. But the processes associated with such homeostasis can be costly and affect the fitness of individuals. As a result, individuals from variable environments are expected to invest more in compensatory mechanisms to maintain homeostasis than individuals from stable environments. Grammostola quirogai and Grammostola anthracina are two spiders of the Theraphosidae family that live in rocky-hill habitats in the Pampas ecoregion. Both species inhabit mesic environments with moderate rainy weather but different precipitation variability. G. quirogai only exists in rocky-hill habitats surrounded by prairies, far from oceanic and estuarine coasts. These habitats are exposed to higher and more variable precipitation rates due to a stronger influence of El Niño. In contrast, G. anthracina lives in areas with less heterogeneous precipitation rates, and its populations expand up to the Atlantic coast. In this study, we used these two species to explore the impacts of water deprivation on their metabolic rate and water loss. We did not detect changes in metabolic rate or differences in water loss as a result of a water restriction treatment in any of the species. However, the mean total values of evaporative water loss for our studied species were lower than that of xeric species. These results provide evidence that the total evaporative water loss in tarantulas may not be related to environmental characteristics, as it has been widely reported among insect species.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2

Similar content being viewed by others

Data availability

The datasets generated during the current study are available in the FigShare repository, doi https://doi.org/10.6084/m9.figshare.8263745

Abbreviations

TEWL:

Total evaporative water loss

SMR:

Standard metabolic rate

References

  • Addo-Bediako A, Chown SL, Gaston KJ (2001) Revisiting water loss in insects: a large scale view. J Insect Physiol 47:1377–1388

    CAS  PubMed  Google Scholar 

  • Aisenberg A, Pérez-Miles F (2016) Uruguayan tarantulas in danger: pet traders strike again. Terrible Tentacle Theatre. http://tentacletheatre.com/post/141213127835/attn-tarantula-keepers.

  • Akaike H (1971) Autoregressive model fitting for control. Ann Inst Stat Math 23:163–180

    Google Scholar 

  • Akaike H (1974) A new look at the statistical model identification. IEEE Trans Autom Contr 19:716–723

    Google Scholar 

  • Anderson JF (1970) Metabolic rates of spiders. Comp Biochem Phys 33:51–72

    CAS  Google Scholar 

  • Barreiro M (2010) Influence of ENSO and the South Atlantic Ocean on climate predictability over Southeastern South America. Clim Dynam 35:1493–1508

    Google Scholar 

  • Canals M, Figueroa D, Alfaro C, Kawamoto T, Torres-Contreras H, Sabat P, Veloso C (2011) Effects of diet and water supply on energy intake and water loss in a mygalomorph spider in a fluctuating environment of the central Andes. J Insect Physiol 57:1489–1494

    CAS  PubMed  Google Scholar 

  • Canals M, Veloso C, Solís R (2015) Adaptation of the spiders to the environment: the case of some Chilean species. Front Physiol 6:220

    PubMed  PubMed Central  Google Scholar 

  • Carlos Perafán, Fernando Pérez-Miles (2014) The Andean tarantulas Ausserer, 1875, Simon, 1892 and Simon, 1889 (Araneae: Theraphosidae): phylogenetic analysis, genera redefinition and new species descriptions . Journal of Natural History 48(39–40):2389–2418

  • Catalán TP, Wozniak A, Niemeyer HM, Kalergis AM, Bozinovic F (2012) Interplay between thermal and immune ecology: effect of environmental temperature on insect immune response and energetic costs after an immune challenge. J Insect Physiol 58:310–317

    PubMed  Google Scholar 

  • Cavieres G, Sabat P (2008) Geographic variation in the response to thermal acclimation in rufous-collared sparrows: are physiological flexibility and environmental heterogeneity correlated? Funct Ecol 22:509–515

    Google Scholar 

  • Chown SL, Gaston KJ (1999) Exploring links between physiology and ecology at macro-scales: the role of respiratory metabolism in insects. Biol Rev 74:87–120

    Google Scholar 

  • Chown SL, Nicolson S (2004) Insect physiological ecology: mechanisms and patterns. Oxford University Press, New York

    Google Scholar 

  • Chown SL, Sørensen JG, Terblanche JS (2011) Water loss in insects: an environmental change perspective. J Insect Physiol 57:1070–1084

    CAS  PubMed  Google Scholar 

  • Cléton F, Sigwalt Y, Verdez JM (2015) Tarantulas, breeding experience & wildlife. Edition Chimaira, Frankfurt

    Google Scholar 

  • Costa FG, Pérez-Miles F (2002) Reproductive biology of uruguayan theraphosids (Araneae, Mygalomorphae). J Arachnol 30:571–587

    Google Scholar 

  • De Voe RS (2009) Captive invertebrate nutrition. Vet Clin North Am Exot Anim Pract 12(2):349–360

    PubMed  Google Scholar 

  • Figueroa D, Sabat P, Torres-Contreras H, Veloso C, Canals M (2010) Participation of book lungs in evaporative water loss in Paraphysa parvula, a migalomorph spider from Chilean Andes. J Insect Physiol 56:731–735

    CAS  PubMed  Google Scholar 

  • Ghione S, Coelho L, Costa FG, García LF, González M, Jorge C, Toscano-Gadea C (2017) Arácnidos prioritarios para la conservación en Uruguay. Bol Soc Zool Uruguay 26(1):1–8

    Google Scholar 

  • Greenstone MH, Bennett AF (1980) Foraging strategy and metabolic rate in spiders. Ecology 61:1255–1259

    Google Scholar 

  • Gutierrez JR et al. (2010) Long-term research in Bosque Fray Jorge National Park: twenty years studying the role of biotic and abiotic factors in a Chilean semiarid scrubland. Rev Chil Hist Nat 83

  • Hadley NF, Ahearn GA, Howarth FG (1981) Water and metabolic relations of cave-adapted and epigean lycosid spiders in Hawaii. J Arachnol: 215–222

  • Hadley NF, Quinlan MC (1989) Cuticular permeability of the black widow spider Latrodectus hesperus. J Comp Physiol B 159:243–248

    Google Scholar 

  • Humphreys W (1975) The influence of burrowing and thermoregulatory behaviour on the water relations of Geolycosa godeffroyi (Araneae: Lycosidae), an Australian wolf spider. Oecologia 21:291–311

    CAS  PubMed  Google Scholar 

  • INUMET 2018. Instituto Uruguayo de Meteorología, Climatología Estacional 1981–2010. www.inumet.gub.uy/clima/climatologia-estacional. Accessed 15 March 2019

  • Jaksic FM (2001) Ecological effects of El Nino in terrestrial ecosystems of western South America. Ecography 24:241–250

    Google Scholar 

  • Janzen DH (1967) Why mountain passes are higher in the tropics. Am Nat 101:233–249

    Google Scholar 

  • Jiménez MA, Jaksic FM, Armesto JJ, Gaxiola A, Meserve PL, Kelt DA, Gutiérrez JR (2011) Extreme climatic events change the dynamics and invasibility of semi-arid annual plant communities. Ecol Lett 14:1227–1235

    PubMed  Google Scholar 

  • Koch CL (1842) Systematische Uebersicht über die familie der Galeoden. Archiv für Naturgeschichte 8: 350–356

  • Lapinski W, Tschapka M (2014) Desiccation resistance reflects patterns of microhabitat choice in a Central American assemblage of wandering spiders. J Exp Biol 217:2789–2795

    PubMed  Google Scholar 

  • Lide DR (2012) Handbook of chemistry and physics. CRC Press, Boca Ratón

    Google Scholar 

  • Lighton JRB (2008) Measuring metabolic rates: a manual for scientists: a manual for scientists. Oxford University Press, New York

    Google Scholar 

  • Lighton JRB, Brownell PH, Joos B, Turner RJ (2001) Low metabolic rate in scorpions: implications for population biomass and cannibalism. J Exp Biol 204:607–613

    CAS  PubMed  Google Scholar 

  • Lima M, Marquet PA, Jaksic FM (1999) El Nino events, precipitation patterns, and rodent outbreaks are statistically associated in semiarid Chile. Ecography 22:213–218

    Google Scholar 

  • McNab BK (2002) The physiological ecology of vertebrates: a view from energetics. Cornell University Press

  • Montes de Oca L, D'Elía G, Pérez-Miles F (2015) An integrative approach for species delimitation in the spider genus Grammostola (Theraphosidae, Mygalomorphae). Zool Scr 45(3):322–333

    Google Scholar 

  • Nespolo RF, Correa L, Pérez-Apablaza CX, Cortés P, Bartheld JL (2011) Energy metabolism and the postprandial response of the Chilean tarantulas, Euathlus truculentus (Araneae: Theraphosidae). Comp Biochem Phys A 159:379–382

    Google Scholar 

  • Paaijmans KP, Heinig RL, Seliga RA, Blanford JI, Blanford S, Murdock CC, Thomas MB (2013) Temperature variation makes ectotherms more sensitive to climate change. Glob Change Biol 19(8):2373–2380

    Google Scholar 

  • Paul R, Fincke T, Linzen B (1987) Respiration in the tarantula Eurypelma californicum: evidence for diffusion lungs. J Comp Physiol B 157:209–217

    Google Scholar 

  • Piersma T, Drent J (2003) Phenotypic flexibility and the evolution of organismal design. Trends Ecol Evol 18:228–233

    Google Scholar 

  • Pigliucci M (2001) Phenotypic plasticity: beyond nature and nurture. JHU Press, Baltimore

    Google Scholar 

  • Pocock RI (1903) On some genera and species of South-American Aviculariidae. J Nat Hist 11(61): 81–115

  • Previtali MA, Lima M, Meserve PL, Kelt DA, Gutiérrez JR (2009) Population dynamics of two sympatric rodents in a variable environment: rainfall, resource availability, and predation. Ecology 90:1996–2006

    PubMed  Google Scholar 

  • Schilman PE, Lighton JR, Holway DA (2005) Respiratory and cuticular water loss in insects with continuous gas exchange: comparison across five ant species. Jn Insect Physiol 51:1295–1305

    CAS  Google Scholar 

  • Shillington C (2005) Inter-sexual differences in resting metabolic rates in the Texas tarantula, Aphonopelma anax. Comp Biochem Phys A 142:439–445

    Google Scholar 

  • Shillington C, Peterson CC (2002) Energy metabolism of male and female tarantulas (Aphonopelma anax) during locomotion. J Exp Biol 205:2909–2914

    PubMed  Google Scholar 

  • Sinclair BJ, Addo-Bediako A, Chown SL (2003) Climatic variability and the evolution of insect freeze tolerance. Biol Rev 78:181–195

    PubMed  Google Scholar 

  • Stenseth NC, Mysterud A, Ottersen G, Hurrell JW, Chan K-S, Lima M (2002) Ecological effects of climate fluctuations. Science 297:1292–1296

    CAS  PubMed  Google Scholar 

  • Tieleman BI, Williams JB (2000) The adjustment of avian metabolic rates and water fluxes to desert environments. Physiol Biochem Zool 73:461–479

    CAS  PubMed  Google Scholar 

  • Vidiella PE, Armesto JJ, Gutiérrez JR (1999) Vegetation changes and sequential flowering after rain in the southern Atacama Desert. J Arid Environ 43:449–458

    Google Scholar 

  • Weiner J (1992) Physiological limits to sustainable energy budgets in birds and mammals: ecological implications. Trends Ecol Evol 7:384–388

    CAS  PubMed  Google Scholar 

  • WSC. World Spider Catalog (2020). Natural History Museum Bern. https://wsc.nmbe.ch. Accesed 10 February 2020

  • Zuur AF, Ieno EN, Walker NJ, Saveliev AA, Smith GM (2009) Mixed effects models and extensions in ecology with R. Springer Science+Business Media, New York

    Google Scholar 

Download references

Acknowledgments

We thank Laura Montes de Oca for help during the animal husbandry, the personnel of Reserva Natura Salus for access to the Park, the Instituto Uruguayo de Metereología (INUMET) for providing data on precipitation and temperature for our sampling sites, and Grisel Cavieres for insightful comments during the experiment and manuscript preparation.

Funding

SCB further thanks PEDECIBA for research funds and Fondecyt N° 11160839.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Sabrina Clavijo-Baquet.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.

Additional information

Communicated by: Paula Roig Boixeda

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Clavijo-Baquet, S., Alfaro, M. & Pérez-Miles, F. Metabolism and water loss are not related to environmental heterogeneity in two mygalomorph spiders. Sci Nat 107, 17 (2020). https://doi.org/10.1007/s00114-020-1672-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00114-020-1672-3

Keywords

Navigation