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Metabolic costs imposed by hydrostatic pressure constrain bathymetric range in the lithodid crab Lithodes maja.
Brown, Alastair; Thatje, Sven; Morris, James P; Oliphant, Andrew; Morgan, Elizabeth A; Hauton, Chris; Jones, Daniel O B; Pond, David W.
Afiliação
  • Brown A; University of Southampton, Ocean and Earth Science, European Way, Southampton SO14 3ZH, UK alastair.brown@noc.soton.ac.uk.
  • Thatje S; University of Southampton, Ocean and Earth Science, European Way, Southampton SO14 3ZH, UK.
  • Morris JP; University of Southampton, Ocean and Earth Science, European Way, Southampton SO14 3ZH, UK.
  • Oliphant A; University of Southampton, Ocean and Earth Science, European Way, Southampton SO14 3ZH, UK.
  • Morgan EA; University of Southampton, Ocean and Earth Science, European Way, Southampton SO14 3ZH, UK.
  • Hauton C; University of Southampton, Ocean and Earth Science, European Way, Southampton SO14 3ZH, UK.
  • Jones DOB; National Oceanography Centre, University of Southampton Waterfront Campus, European Way, Southampton SO14 3ZH, UK.
  • Pond DW; Scottish Association for Marine Science, Oban, Argyll PA37 1QA, UK.
J Exp Biol ; 220(Pt 21): 3916-3926, 2017 11 01.
Article em En | MEDLINE | ID: mdl-29093188
ABSTRACT
The changing climate is shifting the distributions of marine species, yet the potential for shifts in depth distributions is virtually unexplored. Hydrostatic pressure is proposed to contribute to a physiological bottleneck constraining depth range extension in shallow-water taxa. However, bathymetric limitation by hydrostatic pressure remains undemonstrated, and the mechanism limiting hyperbaric tolerance remains hypothetical. Here, we assess the effects of hydrostatic pressure in the lithodid crab Lithodes maja (bathymetric range 4-790 m depth, approximately equivalent to 0.1 to 7.9 MPa hydrostatic pressure). Heart rate decreased with increasing hydrostatic pressure, and was significantly lower at ≥10.0 MPa than at 0.1 MPa. Oxygen consumption increased with increasing hydrostatic pressure to 12.5 MPa, before decreasing as hydrostatic pressure increased to 20.0 MPa; oxygen consumption was significantly higher at 7.5-17.5 MPa than at 0.1 MPa. Increases in expression of genes associated with neurotransmission, metabolism and stress were observed between 7.5 and 12.5 MPa. We suggest that hyperbaric tolerance in Lmaja may be oxygen-limited by hyperbaric effects on heart rate and metabolic rate, but that Lmaja's bathymetric range is limited by metabolic costs imposed by the effects of high hydrostatic pressure. These results advocate including hydrostatic pressure in a complex model of environmental tolerance, where energy limitation constrains biogeographic range, and facilitate the incorporation of hydrostatic pressure into the broader metabolic framework for ecology and evolution. Such an approach is crucial for accurately projecting biogeographic responses to changing climate, and for understanding the ecology and evolution of life at depth.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anomuros / Metabolismo Energético / Distribuição Animal Tipo de estudo: Health_economic_evaluation Limite: Animals Idioma: En Revista: J Exp Biol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anomuros / Metabolismo Energético / Distribuição Animal Tipo de estudo: Health_economic_evaluation Limite: Animals Idioma: En Revista: J Exp Biol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Reino Unido