This document summarizes a study on the effects of ocean acidification on the development and physiology of Pacific oyster larvae. The study exposed oyster larvae to different levels of CO2 representing current and elevated future atmospheric CO2 levels. Results showed higher CO2 levels delayed development, decreased calcification and growth, and increased expression of stress response genes. The study suggests ocean acidification could negatively impact oyster larvae development and physiology.
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How ocean acidification affects Pacific oyster larval development and physiology
1. The Effects of Ocean Acidification on
Pacific Oyster Larval Development
and Physiology
Emma Timmins-Schiffman
Steven Roberts
Carolyn Friedman
Michael O’Donnell
University of Washington
PCSGA
Salem, OR, September, 2011
2. How does OA affect larvae?
Effect of OA Organism Reference
Decreased shell Oyster, mussel, 1, 2, 3, 4, 9, 12
size, strength, barnacle, crab
calcification
Transcriptome/ Urchin 5, 6, 10
physiology
Protein Barnacle 7
Developmental Urchin, shrimp, 8, 9, 13
delay and change brittle star
in energy budget
Increased growth Sea star 11
rate
Abnormal Brittle star, urchin, 12, 2
morphology oyster
Response to other Urchin, barnacle, 14, 3
stressors crab
3. Which physiological mechanisms are
changing?
¤ Calcification
¤ Hydrogen ion balance across membranes
¤ Energy metabolism
¤ Timing of developmental processes
¤ Stress response
4. How does ocean acidification affect
development and physiology of Pacific oyster
larvae (Crassostrea gigas)
5. CO2-free air
CO2 (canister)
Honeywell Controller
Treatment-
equilibrated
water
DuraFET pH probe Venturi injector
6. Experimental Design
Equilibrate treatment water
Fertilization 1 hpf 6 hpf 24 hpf 72 hpf 96 hpf
Fix samples for
Sample for transcriptomics
developmental stage, size,
and calcification
11. Results: Larval Development, Growth,
and Calcification
¤ Larvae were fixed for later microscopy
¤ Developmental stage was assessed
¤ Growth was measured: hinge length, shell
height
¤ Calcification: double polarization of light
12. Proportion Larvae at Pre-Hatching Stage at 6hpf
1.0
400 !atm
700 !atm
1000 !atm
0.8
Proportion at Pre-Hatching
Significantly
0.6
fewer larvae are
in an advanced
0.4
developmental
stage at higher
pCO2 (lower pH)
0.2
0.0
400 700 1000
Treatment
14. Larval Calcification at 24h
More larvae
1.0
400 !atm
700 !atm have started
1000 !atm calcification
0.8
at higher
Proportion Calcified
pCO2
0.6
0.4
0.2
0.0
400 700 1000
Treatment
15. Larval Calcification at 72h
Fewer larvae
1.0
are fully
calcified in
the highest
0.8
pCO2
Proportion Calcified
(lowest pH)
0.6
treatment
0.4
400 !atm
0.2
700 !atm
1000 !atm
0.0
400 700 1000
Treatment
16. Larval Size: Methods
¤ Size measured in 2
parameters – hinge
length and shell
height
¤ Measurements are
from 24 and 72
hours post
fertilization
17. Hinge Length by Treatment and Day Shell Height by Treatment and Day
80
70
70
60
Hinge Length (!m)
Shell Height (!m)
50
60
40
50
30
40
D1 400 D1 700 D1 1000 D3 400 D3 700 D3 1000
D1 400 D1 700 D1 1000 D3 400 D3 700 D3 1000
Day and pCO2 (!atm)
Day and pCO2 (!atm)
Larvae are smaller at higher pCO2 at 3
days post-fertilization
18. Growth Rate by Treatment
15
Hinge
Height
Shell height
Growth Rate/Day (!m)
10
growth rate is
slower at the
highest pCO2
5
0
400 700 1000
Treatment (!atm)
19. Gene Expression
¤ 2 microcosms from
each treatment at
96 hpf
¤ Oxidative stress
genes (SOD,Prx6)
and molecular
chaperone (Hsp70)
20. Hsp70
Stress Response
STRESS Protein damage/
unfolding
Hsp70
Chaperones bind to proteins to either repair or remove
21. Heat Shock Protein 70
25
Fold Over Minimum Expression
Increased
20
expression
of hsp70
with
15
increased
pCO2 could
indicate
10
cellular
stress
5
400 700 1000
Treatment (!atm)
25. Oxidative Stress Genes
Greater expression of SOD and Prx6 may
indicate increased oxidative stress during
exposure to ocean acidification
26. Conclusions
¤ pCO2 of 700 and 1000 µatm caused decreased growth
and calcification in C .gigas larvae through 72 hpf
¤ There is evidence of physiological stress
¤ Significant for exposure to other stressors
¤ Significant for continued growth, development, and survival
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28. References
¤ 1Watson et al. 2009. Early larval development of the Sydney rock oyster Saccostrea glomerata under near-future predictions of CO2-driven ocean acification. Journal of Shellfish Research. 28
(3)): 431-437.
¤ 2 Gaylord et al. 2011 Functional impacts of ocean acidification in an ecologically critical foundation species. J Exp Biol. 214: 2586-2594.
¤ 3 Parker et al. 2010. Comparing the effect of elevated pCO2 and temperature on the fertilization and early development of 2 species of oyster. Marine Biology. 157(11): 2435-2452.
¤ 4 Findlay et al. 2009. Post-larval development of 2 intertidal barnacles at elevated CO2 and temperature. Mar Biol. 157: 725-735.
¤ 5 Todham & Hofmann 2009 Transcriptomic response of sea urchin larvae Strongylocentrotus purpuratus to CO2-driven seawater acidification. J Exp Biol. 212: 2579-2594.
¤ 6 Stumpp et all. 2011. CO2 induced seawater acidification impacts sea urchin larval development II: Gene expression patterns in pluteus larvae. Comparative Biochemistry and Physiology – Part
A. 160(3): 320-330.
¤ 7 Wong et al. 2011. Response of larval barnacle proteome to CO2-driven seawater acidification. Comparative Biochemistry and Physiology – Part D. 6(3): 310-321.
¤ 8 Stumpp et al. 2011. CO2 induced seawater acidification impacts sea urchin larval development I: Elevated metabolic rates decrease scope for growth and induce developmental delay.
Comparative Biochemistry and Physiology – Part A. 160(3): 331-340.
¤ 9 Bechmann et al 2011. Effects of ocean aciidification on early life stages of shrimp (Pandalus borealis) and mussel (Mytilus edulis). J Toxicol Environ Health. 74(7-9): 424-438.
¤ 10 Martin et al. 2011. Early development andmolecular plasticity in the Mediterranean sea urchin Paracentrotus lividus exposed to CO2-driven aciidification. J Exp Biol. 214(8): 1357-1368.
¤ 11 DuPont et al. 2010. Near future ocean acidification increases growth of lecithotrophic larvae and juveniles of the sea star Crossaster papposus. J Exp Biol Part B. 314B(5): 382-389.
¤ 12 Kurihara et al. 2007. Effects of increased seawater pCO2 on early development of the oyster C.rassostrea gigas. Aquat Biol. 1:91-98.
¤ 13 Dupont et al. 2008. Near-future level of CO2-driven ocean acidification radically affects larval survival and development in the brittlestar Ophiothrix fragilis. Mar Ecol Prog Ser. 373: 285-294.
¤ 14 O’Donnell et al. 2009. Predicted impact of ocean acidification on marine invertebrate larvae: elevated CO2 alters response to thermal stress in sea urchin larvae. 156(3): 439-446.