2016
DOI: 10.1111/eva.12391
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Can trans‐generational experiments be used to enhance species resilience to ocean warming and acidification?

Abstract: Human‐assisted, trans‐generational exposure to ocean warming and acidification has been proposed as a conservation and/or restoration tool to produce resilient offspring. To improve our understanding of the need for and the efficacy of this approach, we characterized life‐history and physiological responses in offspring of the marine polychaete Ophryotrocha labronica exposed to predicted ocean warming (OW: + 3°C), ocean acidification (OA: pH −0.5) and their combination (OWA: + 3°C, pH −0.5), following the expo… Show more

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Cited by 43 publications
(69 citation statements)
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“…The effects of parental conditioning are not confined to vertebrates; parental exposure to acidification (+1150 µatm P CO2 ) halved the reduction in fecundity caused by acute exposure to the same conditions in offspring of the copepod Pseudocalanus acuspes (Thor and Dupont, 2015), while parental exposure to ocean warming and acidification (+2°C and +400 µatm P CO2 ) reduced the negative effects of acute exposure on larval size in the coral Pocillopora damicornis . However, parental and acute exposure to combined global change drivers does not always affect the progeny, despite the negative effects of singlestressor exposure, as shown recently in the marine polychaete Ophryotroca labronica (Chakravarti et al, 2016).…”
Section: Introductionmentioning
confidence: 82%
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“…The effects of parental conditioning are not confined to vertebrates; parental exposure to acidification (+1150 µatm P CO2 ) halved the reduction in fecundity caused by acute exposure to the same conditions in offspring of the copepod Pseudocalanus acuspes (Thor and Dupont, 2015), while parental exposure to ocean warming and acidification (+2°C and +400 µatm P CO2 ) reduced the negative effects of acute exposure on larval size in the coral Pocillopora damicornis . However, parental and acute exposure to combined global change drivers does not always affect the progeny, despite the negative effects of singlestressor exposure, as shown recently in the marine polychaete Ophryotroca labronica (Chakravarti et al, 2016).…”
Section: Introductionmentioning
confidence: 82%
“…100 worms) was collected from a single site in Porto Empedocle harbor (Sicily, Italy: 37°17′N, 13°3 1′E) in January 2014 (Chakravarti et al, 2016). The culture was transferred to the Marine Evolutionary Physiology (MEP) laboratory at the Université du Québec à Rimouski (Canada), where it was kept for eight generations under control conditions (temperature 27°C, pH 8, salinity 35, 12 h light:12 h dark), selected to maximize reproductive output (Åkesson, 1970).…”
Section: Collection and Establishment Of The Culturementioning
confidence: 99%
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“…Thermal preconditioning in marine ectotherms often involves altered carbohydrate metabolism and aerobic respiration (Sokolova and Pörtner, 2003;Sommer and Pörtner, 2004;Kraffe et al, 2007;Pörtner et al, 2007;Oellermann et al, 2012;Chung and Schulte, 2015), notably through the regulation of mitochondrial function (Somero and Hochachka, 2002). For example, increasing mitochondrial density and aerobic capacity is a common adaptive response to cold conditions ( polychaetes: Sommer and Pörtner, 1999;polar marine invertebrates: Pörtner, 2001;Peck, 2002;Pörtner et al, 2007), while warm acclimation often correlates with decreased mitochondrial density/aerobic capacity (rainbow trout: Kraffe et al, 2007; polychaetes: Chakravarti et al, 2016) and reduced sensitivity to short-term heating (killifish: Chung and Schulte, 2015). Warm preconditioning in corals may occur through similar processes.…”
Section: Introductionmentioning
confidence: 99%