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Abstract Coastal habitats are experiencing decreases in seawater pH and increases in temperature due to anthropogenic climate change. The Caribbean king crab,Maguimithrax spinosissimus, plays a vital role on Western Atlantic reefs by grazing macroalgae that competes for space with coral recruits. Therefore, identifying its tolerance to anthropogenic stressors is critically needed if this species is to be considered as a potential restoration management strategy in coral reef environments. We examined the effects of temperature (control: 28 °C and elevated: 31 °C) and pH (control: 8.0 and reduced pH: 7.7) on the king crab’s larval and early juvenile survival, molt-stage duration, and morphology in a fully crossed laboratory experiment. Survival to the megalopal stage was reduced (13.5% lower) in the combined reduced pH and elevated temperature treatment relative to the control. First-stage (J1) juveniles delayed molting by 1.5 days in the reduced pH treatment, while second-stage (J2) crabs molted 3 days earlier when exposed to elevated temperature. Juvenile morphology did not differ among treatments. These results suggests that juvenile king crabs are tolerant to changes associated with climate change. Given the important role of the king crab as a grazer of macroalgae, its tolerance to climate stressors suggests that it could benefit restoration efforts aimed at making coral reefs more resilient to increasingly warm and acidic oceans into the future.
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The Marine Gastropod Crepidula fornicata Remains Resilient to Ocean Acidification Across Two Life History Stages
Rising atmospheric CO 2 reduces seawater pH causing ocean acidification (OA). Understanding how resilient marine organisms respond to OA may help predict how community dynamics will shift as CO 2 continues rising. The common slipper shell snail Crepidula fornicata is a marine gastropod native to eastern North America that has been a successful invader along the western European coastline and elsewhere. It has also been previously shown to be resilient to global change stressors. To examine the mechanisms underlying C. fornicata’s resilience to OA, we conducted two controlled laboratory experiments. First, we examined several phenotypes and genome-wide gene expression of C. fornicata in response to pH treatments (7.5, 7.6, and 8.0) throughout the larval stage and then tested how conditions experienced as larvae influenced juvenile stages (i.e., carry-over effects). Second, we examined genome-wide gene expression patterns of C. fornicata larvae in response to acute (4, 10, 24, and 48 h) pH treatment (7.5 and 8.0). Both C. fornicata larvae and juveniles exhibited resilience to OA and their gene expression responses highlight the role of transcriptome plasticity in this resilience. Larvae did not exhibit reduced growth under OA until they were at least 8 days old. These phenotypic effects were preceded by broad transcriptomic changes, which likely served as an acclimation mechanism for combating reduced pH conditions frequently experienced in littoral zones. Larvae reared in reduced pH conditions also took longer to become competent to metamorphose. In addition, while juvenile sizes at metamorphosis reflected larval rearing pH conditions, no carry-over effects on juvenile growth rates were observed. Transcriptomic analyses suggest increased metabolism under OA, which may indicate compensation in reduced pH environments. Transcriptomic analyses through time suggest that these energetic burdens experienced under OA eventually dissipate, allowing C. fornicata to reduce metabolic demands and acclimate to reduced pH. Carry-over effects from larval OA conditions were observed in juveniles; however, these effects were larger for more severe OA conditions and larvae reared in those conditions also demonstrated less transcriptome elasticity. This study highlights the importance of assessing the effects of OA across life history stages and demonstrates how transcriptomic plasticity may allow highly resilient organisms, like C. fornicata , to acclimate to reduced pH environments.
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- Award ID(s):
- 1659605
- PAR ID:
- 10322480
- Date Published:
- Journal Name:
- Frontiers in Physiology
- Volume:
- 12
- ISSN:
- 1664-042X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.3389/fphys.2021.702864
