Cuticular gas exchange by Antarctic sea spiders

Many marine organisms and life stages lack specialized respiratory structures, like gills, and rely instead on cutaneous respiration, which they facilitate by having thin integuments. This respiratory mode may limit body size, especially if the integument also functions in support or locomotion. Pyc...

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Published in:Journal of Experimental Biology
Main Authors: Lane, Steven J., Moran, Amy L., Shishido, Caitlin M., Tobalske, Bret W., Woods, H. Arthur
Format: Text
Language:English
Published: The Company of Biologists Ltd 2018
Subjects:
Online Access:http://jeb.biologists.org/cgi/content/short/221/8/jeb177568
https://doi.org/10.1242/jeb.177568
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spelling fthighwire:oai:open-archive.highwire.org:jexbio:221/8/jeb177568 2023-05-15T14:02:51+02:00 Cuticular gas exchange by Antarctic sea spiders Lane, Steven J. Moran, Amy L. Shishido, Caitlin M. Tobalske, Bret W. Woods, H. Arthur 2018-04-25 01:29:43.0 text/html http://jeb.biologists.org/cgi/content/short/221/8/jeb177568 https://doi.org/10.1242/jeb.177568 en eng The Company of Biologists Ltd http://jeb.biologists.org/cgi/content/short/221/8/jeb177568 http://dx.doi.org/10.1242/jeb.177568 Copyright (C) 2018, Company of Biologists RESEARCH ARTICLE TEXT 2018 fthighwire https://doi.org/10.1242/jeb.177568 2018-12-30T19:26:17Z Many marine organisms and life stages lack specialized respiratory structures, like gills, and rely instead on cutaneous respiration, which they facilitate by having thin integuments. This respiratory mode may limit body size, especially if the integument also functions in support or locomotion. Pycnogonids, or sea spiders, are marine arthropods that lack gills and rely on cutaneous respiration but still grow to large sizes. Their cuticle contains pores, which may play a role in gas exchange. Here, we examined alternative paths of gas exchange in sea spiders: (1) oxygen diffuses across pores in the cuticle, a common mechanism in terrestrial eggshells, (2) oxygen diffuses directly across the cuticle, a common mechanism in small aquatic insects, or (3) oxygen diffuses across both pores and cuticle. We examined these possibilities by modeling diffusive oxygen fluxes across all pores in the body of sea spiders and asking whether those fluxes differed from measured metabolic rates. We estimated fluxes across pores using Fick's law parameterized with measurements of pore morphology and oxygen gradients. Modeled oxygen fluxes through pores closely matched oxygen consumption across a range of body sizes, which means the pores facilitate oxygen diffusion. Furthermore, pore volume scaled hypermetrically with body size, which helps larger species facilitate greater diffusive oxygen fluxes across their cuticle. This likely presents a functional trade-off between gas exchange and structural support, in which the cuticle must be thick enough to prevent buckling due to external forces but porous enough to allow sufficient gas exchange. Text Antarc* Antarctic HighWire Press (Stanford University) Antarctic Journal of Experimental Biology
institution Open Polar
collection HighWire Press (Stanford University)
op_collection_id fthighwire
language English
topic RESEARCH ARTICLE
spellingShingle RESEARCH ARTICLE
Lane, Steven J.
Moran, Amy L.
Shishido, Caitlin M.
Tobalske, Bret W.
Woods, H. Arthur
Cuticular gas exchange by Antarctic sea spiders
topic_facet RESEARCH ARTICLE
description Many marine organisms and life stages lack specialized respiratory structures, like gills, and rely instead on cutaneous respiration, which they facilitate by having thin integuments. This respiratory mode may limit body size, especially if the integument also functions in support or locomotion. Pycnogonids, or sea spiders, are marine arthropods that lack gills and rely on cutaneous respiration but still grow to large sizes. Their cuticle contains pores, which may play a role in gas exchange. Here, we examined alternative paths of gas exchange in sea spiders: (1) oxygen diffuses across pores in the cuticle, a common mechanism in terrestrial eggshells, (2) oxygen diffuses directly across the cuticle, a common mechanism in small aquatic insects, or (3) oxygen diffuses across both pores and cuticle. We examined these possibilities by modeling diffusive oxygen fluxes across all pores in the body of sea spiders and asking whether those fluxes differed from measured metabolic rates. We estimated fluxes across pores using Fick's law parameterized with measurements of pore morphology and oxygen gradients. Modeled oxygen fluxes through pores closely matched oxygen consumption across a range of body sizes, which means the pores facilitate oxygen diffusion. Furthermore, pore volume scaled hypermetrically with body size, which helps larger species facilitate greater diffusive oxygen fluxes across their cuticle. This likely presents a functional trade-off between gas exchange and structural support, in which the cuticle must be thick enough to prevent buckling due to external forces but porous enough to allow sufficient gas exchange.
format Text
author Lane, Steven J.
Moran, Amy L.
Shishido, Caitlin M.
Tobalske, Bret W.
Woods, H. Arthur
author_facet Lane, Steven J.
Moran, Amy L.
Shishido, Caitlin M.
Tobalske, Bret W.
Woods, H. Arthur
author_sort Lane, Steven J.
title Cuticular gas exchange by Antarctic sea spiders
title_short Cuticular gas exchange by Antarctic sea spiders
title_full Cuticular gas exchange by Antarctic sea spiders
title_fullStr Cuticular gas exchange by Antarctic sea spiders
title_full_unstemmed Cuticular gas exchange by Antarctic sea spiders
title_sort cuticular gas exchange by antarctic sea spiders
publisher The Company of Biologists Ltd
publishDate 2018
url http://jeb.biologists.org/cgi/content/short/221/8/jeb177568
https://doi.org/10.1242/jeb.177568
geographic Antarctic
geographic_facet Antarctic
genre Antarc*
Antarctic
genre_facet Antarc*
Antarctic
op_relation http://jeb.biologists.org/cgi/content/short/221/8/jeb177568
http://dx.doi.org/10.1242/jeb.177568
op_rights Copyright (C) 2018, Company of Biologists
op_doi https://doi.org/10.1242/jeb.177568
container_title Journal of Experimental Biology
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