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Bibliographic Details
Main Authors: Ern, Rasmus, Esbaugh, Andrew J
Format: Dataset Open Access
Language:en
Published: PANGAEA 2016
Subjects:
Alkalinity, total; Alkalinity, total, standard error; Animalia; Aragonite saturation state; Behaviour; Bicarbonate ion; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure, blood; Carbon dioxide, partial pressure, blood, standard error; Carbon dioxide, standard error; Chordata; Coast and continental shelf; Containers and aquaria (20-1000 L or < 1 m**2); Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Laboratory experiment; Nekton; North Atlantic; OA-ICC; Ocean acidification; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air), standard error; Pelagos; pH; pH, NBS scale; pH, standard error; pH, total scale; Potentiometric; Potentiometric titration; Registration number of species; Salinity; Sciaenops ocellatus; Single species; Species; Temperate; Temperature, water; Temperature, water, standard error; Time in hours; Treatment; Type; Uniform resource locator/link to reference; Ventilation amplitude, relative; Ventilation amplitude, relative, standard error; Ventilation frequency; Ventilation frequency, standard error; Ventilation stroke volume, relative; Ventilation stroke volume, relative, standard error; Ventilatory minute volume, relative; Ventilatory minute volume, relative, standard error
Online Access:https://doi.org/10.1594/PANGAEA.869471
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author Ern, Rasmus
Esbaugh, Andrew J
author_facet Ern, Rasmus
Esbaugh, Andrew J
collection Datos científicos de ciencias marinas y ambientales
contents Hyperventilation is a common response in fish exposed to elevated water CO2. It is believed to lessen the respiratory acidosis associated with hypercapnia by lowering arterial PCO2, but the contribution of hyperventilation to blood acid-base compensation has yet to be quantified. Hyperventilation may also increase the flux of irons across the gill epithelium and the cost of osmoregulation, owing to the osmo-respiratory compromise. Therefore, hypercapnia exposed fish may increase standard metabolic rate (SMR) leaving less energy for physiological functions such as foraging, migration, growth and reproduction. Here we show that gill ventilation, blood PCO2 and total blood [CO2] increased in red drum (Sciaenops ocellatus) exposed to 1000 and 5000 µatm water CO2, and that blood PCO2 and total blood [CO2] decrease in fish during hypoxia induced hyperventilation. Based on these results we estimate the ventilatory contributions to total acid-base compensation in 1000 and 5000 µatm water CO2. We find that S. ocellatus only utilize a portion of its ventilatory capacity to reduce the acid-base disturbance in 1000 µatm water CO2. SMR was unaffected by both salinity and hypercapnia exposure indicating that the cost of osmoregulation is small relative to SMR, and that the lack of increased ventilation in 1000 µatm water CO2 despite the capacity to do so is not due to an energetic tradeoff between acid-base balance and osmoregulation. Therefore, while ocean acidification may impact ventilatory parameters, there will be little impact on the overall energy budget of S. ocellatus.
format Dataset Open Access
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institution PANGAEA
language en
publishDate 2016
publisher PANGAEA
record_format pangaea
spellingShingle Hyperventilation and blood acid-base balance in hypercapnia exposed red drum (Sciaenops ocellatus)
Ern, Rasmus
Esbaugh, Andrew J
Alkalinity, total; Alkalinity, total, standard error; Animalia; Aragonite saturation state; Behaviour; Bicarbonate ion; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure, blood; Carbon dioxide, partial pressure, blood, standard error; Carbon dioxide, standard error; Chordata; Coast and continental shelf; Containers and aquaria (20-1000 L or < 1 m**2); Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Laboratory experiment; Nekton; North Atlantic; OA-ICC; Ocean acidification; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air), standard error; Pelagos; pH; pH, NBS scale; pH, standard error; pH, total scale; Potentiometric; Potentiometric titration; Registration number of species; Salinity; Sciaenops ocellatus; Single species; Species; Temperate; Temperature, water; Temperature, water, standard error; Time in hours; Treatment; Type; Uniform resource locator/link to reference; Ventilation amplitude, relative; Ventilation amplitude, relative, standard error; Ventilation frequency; Ventilation frequency, standard error; Ventilation stroke volume, relative; Ventilation stroke volume, relative, standard error; Ventilatory minute volume, relative; Ventilatory minute volume, relative, standard error
Hyperventilation is a common response in fish exposed to elevated water CO2. It is believed to lessen the respiratory acidosis associated with hypercapnia by lowering arterial PCO2, but the contribution of hyperventilation to blood acid-base compensation has yet to be quantified. Hyperventilation may also increase the flux of irons across the gill epithelium and the cost of osmoregulation, owing to the osmo-respiratory compromise. Therefore, hypercapnia exposed fish may increase standard metabolic rate (SMR) leaving less energy for physiological functions such as foraging, migration, growth and reproduction. Here we show that gill ventilation, blood PCO2 and total blood [CO2] increased in red drum (Sciaenops ocellatus) exposed to 1000 and 5000 µatm water CO2, and that blood PCO2 and total blood [CO2] decrease in fish during hypoxia induced hyperventilation. Based on these results we estimate the ventilatory contributions to total acid-base compensation in 1000 and 5000 µatm water CO2. We find that S. ocellatus only utilize a portion of its ventilatory capacity to reduce the acid-base disturbance in 1000 µatm water CO2. SMR was unaffected by both salinity and hypercapnia exposure indicating that the cost of osmoregulation is small relative to SMR, and that the lack of increased ventilation in 1000 µatm water CO2 despite the capacity to do so is not due to an energetic tradeoff between acid-base balance and osmoregulation. Therefore, while ocean acidification may impact ventilatory parameters, there will be little impact on the overall energy budget of S. ocellatus.
title Hyperventilation and blood acid-base balance in hypercapnia exposed red drum (Sciaenops ocellatus)
topic Alkalinity, total; Alkalinity, total, standard error; Animalia; Aragonite saturation state; Behaviour; Bicarbonate ion; Calcite saturation state; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, partial pressure, blood; Carbon dioxide, partial pressure, blood, standard error; Carbon dioxide, standard error; Chordata; Coast and continental shelf; Containers and aquaria (20-1000 L or < 1 m**2); Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Laboratory experiment; Nekton; North Atlantic; OA-ICC; Ocean acidification; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air), standard error; Pelagos; pH; pH, NBS scale; pH, standard error; pH, total scale; Potentiometric; Potentiometric titration; Registration number of species; Salinity; Sciaenops ocellatus; Single species; Species; Temperate; Temperature, water; Temperature, water, standard error; Time in hours; Treatment; Type; Uniform resource locator/link to reference; Ventilation amplitude, relative; Ventilation amplitude, relative, standard error; Ventilation frequency; Ventilation frequency, standard error; Ventilation stroke volume, relative; Ventilation stroke volume, relative, standard error; Ventilatory minute volume, relative; Ventilatory minute volume, relative, standard error
url https://doi.org/10.1594/PANGAEA.869471