Copepod vital rates under CO2-induced acidification: a calanoid species and a cyclopoid species under short-term exposures

Although copepods have been considered tolerant against the direct influence of the ocean acidification (OA) projected for the end of the century, some recent studies have challenged this view. Here, we have examined the direct impact of short-term exposure to a pCO 2 / pH level relevant for the year 2100 ( pH NBS , control: 8.18, low pH : 7.78), on the physiological performance of two representative marine copepods: the calanoid Acartia grani and the cyclopoid Oithona davisae . Adults of both species, from laboratory cultures, were preconditioned for four consecutive days in algal suspensions ( Akashiwo sanguinea ) prepared with filtered sea water pre-adjusted to the targeted pH values via CO 2 bub-bling. We measured the feeding and respiratory activity and reproductive output of those pre-conditioned females. The largely unaffected fatty acid composition of the prey offered between OA treatments and controls supports the absence in the study of indirect OA effects (i.e. changes of food nutritional quality). Our results show no direct effect of acidification on the vital rates examined in either copepod species. Our findings are compared with results from previous short- and long-term manipulative experiments on other copepod species.

[1]  S. Dupont,et al.  Transgenerational effects alleviate severe fecundity loss during ocean acidification in a ubiquitous planktonic copepod , 2015, Global change biology.

[2]  P. Thor,et al.  Ocean acidification elicits different energetic responses in an Arctic and a boreal population of the copepod Pseudocalanus acuspes , 2015 .

[3]  Sarah Faulwetter,et al.  Scaling up experimental ocean acidification and warming research: from individuals to the ecosystem , 2015, Global change biology.

[4]  C. Pelejero,et al.  Lack of evidence for elevated CO2-induced bottom-up effects on marine copepods: a dinoflagellate–calanoid prey–predator pair , 2014 .

[5]  A. Brutemark,et al.  Coping with climate change? Copepods experience drastic variations in their physicochemical environment on a diurnal basis , 2014 .

[6]  K. Flynn,et al.  Have we been underestimating the effects of ocean acidification in zooplankton? , 2014, Global change biology.

[7]  E. Saiz,et al.  Feeding rates and prey : predator size ratios of the nauplii and adult females of the marine cyclopoid copepod Oithona davisae , 2014 .

[8]  B. Jenssen,et al.  Multigenerational exposure to ocean acidification during food limitation reveals consequences for copepod scope for growth and vital rates. , 2014, Environmental science & technology.

[9]  K. Flynn,et al.  Parental exposure to elevated pCO2 influences the reproductive success of copepods , 2014, Journal of plankton research.

[10]  A. Brutemark,et al.  The effects of short-term pH decrease on the reproductive output of the copepod Acartia bifilosa – a laboratory study , 2014 .

[11]  D. Altin,et al.  Effects of Elevated Carbon Dioxide (CO2) Concentrations on Early Developmental Stages of the Marine Copepod Calanus finmarchicus Gunnerus (Copepoda: Calanoidae) , 2014, Journal of toxicology and environmental health. Part A.

[12]  B. Niehoff,et al.  Long-term effects of elevated CO₂ and temperature on the Arctic calanoid copepods Calanus glacialis and C. hyperboreus. , 2014, Marine pollution bulletin.

[13]  U. Grote,et al.  Life in a warming ocean: thermal thresholds and metabolic balance of arctic zooplankton , 2014 .

[14]  Laura A. Edwards,et al.  Sensitivity to ocean acidification parallels natural pCO2 gradients experienced by Arctic copepods under winter sea ice , 2013, Proceedings of the National Academy of Sciences.

[15]  B. H. Hansen,et al.  Medium-term exposure of the North Atlantic copepod Calanus finmarchicus (Gunnerus, 1770) to CO 2 -acidified seawater: effects on survival and development , 2013 .

[16]  A. Brutemark,et al.  Projected marine climate change: effects on copepod oxidative status and reproduction , 2013, Ecology and evolution.

[17]  E. Krasakopoulou,et al.  Effects of low pH and raised temperature on egg production, hatching and metabolic rates of a Mediterranean copepod species (Acartia clausi) under oligotrophic conditions. , 2013 .

[18]  Elaine S. Fileman,et al.  Effects of elevated CO2 on the reproduction of two calanoid copepods. , 2013, Marine pollution bulletin.

[19]  K. Schoo,et al.  Increased carbon dioxide availability alters phytoplankton stoichiometry and affects carbon cycling and growth of a marine planktonic herbivore , 2012, Marine Biology.

[20]  W. Hagen,et al.  Trophodynamics and life-cycle strategies of the copepods Temora longicornis and Acartia longiremis in the Central Baltic Sea , 2013 .

[21]  F. Micheli,et al.  Ocean acidification causes ecosystem shifts via altered competitive interactions , 2013 .

[22]  E. Saiz,et al.  Effects of food concentration on egg production and feeding rates of the cyclopoid copepod Oithona davisae , 2013 .

[23]  A. Brutemark,et al.  Maternal Effects May Act as an Adaptation Mechanism for Copepods Facing pH and Temperature Changes , 2012, PloS one.

[24]  A. Weydmann,et al.  Influence of CO2-induced acidification on the reproduction of a key Arctic copepod Calanus glacialis , 2012 .

[25]  Gary S. Caldwell,et al.  Visualisation of the Copepod Female Reproductive System using Confocal Laser Scanning Microscopy and Two-Photon Microscopy , 2012 .

[26]  Gary S. Caldwell,et al.  Ocean acidification induces multi-generational decline in copepod naupliar production with possible conflict for reproductive resource allocation , 2012 .

[27]  U. Sommer,et al.  Ocean Acidification-Induced Food Quality Deterioration Constrains Trophic Transfer , 2012, PloS one.

[28]  K. Gao,et al.  A marine secondary producer respires and feeds more in a high CO2 ocean. , 2012, Marine pollution bulletin.

[29]  D. Mayor,et al.  End of century ocean warming and acidification effects on reproductive success in a temperate marine copepod , 2012 .

[30]  Guizhong Wang,et al.  Impacts of CO2-driven seawater acidification on survival, egg production rate and hatching success of four marine copepods , 2011 .

[31]  S. Ceballos,et al.  Senescence and Sexual Selection in a Pelagic Copepod , 2011, PloS one.

[32]  M. Alcaraz,et al.  Metabolic rates and carbon budget of early developmental stages of the marine cyclopoid copepod Oithona davisae , 2011 .

[33]  R. Feely,et al.  The universal ratio of boron to chlorinity for the North Pacific and North Atlantic oceans , 2010 .

[34]  S. Dupont,et al.  Impact of near-future ocean acidification on echinoderms , 2010, Ecotoxicology.

[35]  C. Brownlee,et al.  From laboratory manipulations to Earth system models: scaling calcification impacts of ocean acidification , 2009 .

[36]  Scott C. Doney,et al.  Ocean acidification: the other CO2 problem. , 2009, Annual review of marine science.

[37]  H. Kurihara,et al.  Effects of high CO2 seawater on the copepod (Acartia tsuensis) through all life stages and subsequent generations. , 2008, Marine pollution bulletin.

[38]  Richard A. Feely,et al.  Impacts of ocean acidification on marine fauna and ecosystem processes , 2008 .

[39]  S. Hay,et al.  CO2-induced acidification affects hatching success in Calanus finmarchicus , 2007 .

[40]  Tsutomu Ikeda,et al.  Lethality of increasing CO2 levels on deep-sea copepods in the western North Pacific , 2006 .

[41]  Shinji Shimode,et al.  Effects of raised CO2 concentration on the egg production rate and early development of two marine copepods (Acartia steueri and Acartia erythraea). , 2004, Marine pollution bulletin.

[42]  U. Riebesell Effects of CO2 Enrichment on Marine Phytoplankton , 2004 .

[43]  D. Robins,et al.  Is Oithona the most important copepod in the world's oceans? , 2001 .

[44]  Susanne Menden-Deuer,et al.  Carbon to volume relationships for dinoflagellates, diatoms, and other protist plankton , 2000 .

[45]  F. F. Pérèz,et al.  IMPROVEMENTS IN A FAST POTENTIOMETRIC SEAWATER ALKALINITY DETERMINATION DETERMINACIÓN POTENCIOMÉTRICA RÁPIDA DE LA ALKALINIDAD EN AGUA DE MAR: PERFECCIONAMIENTO DEL MÉTODO , 2000 .

[46]  A. Dickson Standard potential of the reaction: , and and the standard acidity constant of the ion HSO4− in synthetic sea water from 273.15 to 318.15 K , 1990 .

[47]  F. Millero,et al.  A comparison of the equilibrium constants for the dissociation of carbonic acid in seawater media , 1987 .

[48]  F. F. Pérèz,et al.  A precise and rapid analytical procedure for alkalinity determination , 1987 .

[49]  G. Kattner,et al.  Simple gas-liquid chromatographic method for the simultaneous determination of fatty acids and alcohols in wax esters of marine organisms , 1986 .

[50]  D. Wilson,et al.  Fecundity studies on Acartia tonsa (Copepoda: Calanoida) in standardized culture , 1978 .

[51]  C. Culberson,et al.  MEASUREMENT OF THE APPARENT DISSOCIATION CONSTANTS OF CARBONIC ACID IN SEAWATER AT ATMOSPHERIC PRESSURE1 , 1973 .

[52]  B. Frost EFFECTS OF SIZE AND CONCENTRATION OF FOOD PARTICLES ON THE FEEDING BEHAVIOR OF THE MARINE PLANKTONIC COPEPOD CALANUS PACIFICUS1 , 1972 .

[53]  B. Mr EFFECTS OF SIZE AND CONCENTRATION OF FOOD PARTICLES ON THE FEEDING BEHAVIOR OF THE MARINE PLANKTONIC COPEPOD CALANUS PACIFICUS , 1972 .

[54]  J. Folch,et al.  A simple method for the isolation and purification of total lipides from animal tissues. , 1957, The Journal of biological chemistry.