Parental exposure to elevated pCO2 influences the reproductive success of copepods

Journal of Plankton Research

Volumn 36, Issue 5, 2014, Pages 1165-1174

  Cripps, Gemma ^a,b   Lindeque, Penelope ^b   Flynn, Kevin ^a  

^a SWANSEA UNIVERSITY   (United Kingdom)

^b PLYMOUTH MARINE LABORATORY   (United Kingdom)

Author keywords

copepods; egg hatching rates; elevated pCO2; ocean acidification; parental exposure; spermatogenesis

Indexed keywords

ACIDIFICATION; CARBON DIOXIDE; EGG PRODUCTION; EXPERIMENTAL DESIGN; HATCHING; MARINE ECOSYSTEM; PH; REPRODUCTIVE SUCCESS;

COPEPODA;

EID: 84908304782     PISSN: 01427873     EISSN: 14643774     Source Type: Journal    
DOI: 10.1093/plankt/fbu052     Document Type: Article

References (37)

1. Allen, J. M. B., Miller, G. M., McCormick, M. I. et al. (2014) Parental effects improve escape performance of juvenile reef fish in a high-CO2 world. Proc. Roy. Soc. B., 281, doi: 10.1098/rspb.2013.2179
2. Blackford, J., Jones, N., Proctor, R. et al. (2009) An initial assessment of the potential environmental impact of CO2 escape from marine carbon capture and storage systems. Proceedings of the Institution of Mechanical Engineers, Part A. J Power Energy, 223, 269-280
3. Blades-Eckelbarger, P. I. (1991) Functional morphology of spermatophores and sperm transfer in calanoid copepod. In: Bauer, RT and Martin, JW (eds), Crustacean Sexual Biology. Columbia University Press, New York, pp. 246-270
4. Caldwell, G. S., Fitzer, S., Gillespie, C. S. et al. (2011) Ocean acidification takes sperm back in time. Invertebr. Reprod. Dev., 55, 217-221
5. Cripps, G., Lindeque, P. and Flynn, K. J. (2014) Have we been underestimating the effects of ocean acidification in zooplankton?. Global. Change. Biol., doi: 10.1111/gcb.12582
6. Dickson, A. G. and Millero, F. J. (1987) Comparison of the equilibrium constants for the dissociation of carbonic acid in seawater media. Deep-Sea Res., 34, 1733-1743
7. Drillet, G., Jorgensen, N. O. G., Soresnsen, T. F. et al. (2006) Biochemical and technical observations supporting the use of copepods as live feed organisms in marine larviculture. Aquaculture, 37, 756-772
8. Fitzer, S. C., Bishop, J. D. D. and Caldwell, G. S. (2012a) Visualisation of the copepod female reproductive system using confocal laser scanning microscopy and two-photon microscopy. J. Crustacean. Biol., 32, 685-692
9. Fitzer, S. C., Caldwell, G. S., Close, A. J. et al. (2012b) Ocean acidification induces multi-generational decline in copepod naupliar production with possible conflict for reproductive resource allocation. J. Exp. Mar. Biol. Ecol., 418, 30-36
10. Fitzer, S. C., Caldwell, G. S., Clare, A. S. et al. (2013) Response of copepods to elevated pCO2 and environmental copper as co-stressors- a multigenerational study. PLoS ONE, 8, doi:10.1371/journal.- pone.0071257
11. Fowler, M. S. (2005) Interactions between maternal effects and dispersal. Oikos, 110, 81-90
12. Guillard, R. and Ryther, J. (1962) Studies of marine planktonic diatoms. I. Cyclotella nana Hustedt and Detonula confervacea (Cleve). Can. J. Microbiol., 8, 229-239
13. Halsband, C. and Hirche, H. J. (2001) Reproductive cycles of dominant calanoid copepods in the North Sea. Mar. Ecol. Prog. Ser., 209, 219-229
14. Havenhand, J. N., Buttler, F. R., Thorndyke, M. C. et al. (2008) Near-future levels of ocean acidification reduce fertilization success in a sea urchin. Curr. Biol., 18, 651-652
15. Holmstrup, M., Overgaard, J., Sorensen, T. F. et al. (2006) Influence of storage on the viability of quiescent copepod eggs (Acartia tonsa): effects of temperature, salinity and anoxia. Aquaculture, 37, 625-631
16. Kahan, D. and Berman, Y. (1988) Maternal inhibition of hatching at high population densities in Tigriopus japonicus (Copepoda, Crustacea). Biol. Bull., 174, 139-144
17. Kurihara, H. (2008) Effects of CO2-driven ocean acidification on the early developmental stages of invertebrates. Mar. Ecol. Prog. Ser., 373, 275-284
18. Marshall, D. J., Allen, R. and Crean, A. (2008) The ecological and evolutionary importance of maternal effects in the sea. Oceanogr. Mar. Biol., 46, 203-250
19. Mayor, D., Matthews, C., Cook, K. et al. (2007) CO2-induced acidification affects hatching success in Calanus finmarchicus. Mar. Ecol. Prog. Ser., 350, 91-97
20. McConville, K., Halsband, C., Fileman, E. S. et al. (2013) Effects of elevated CO2 on the reproduction of two calanoid copepods. Mar. Pollut. Bull., 73, 428-434
21. Mehrbrach, C., Culberson, C. H., Hawley, J. E. et al. (1973) Measurement of apparent dissociation-constants of carbonic-acid in seawater at atmospheric pressure. Limnol. Oceanogr., 18, 897-907
22. Miller, G. M.,Watson, S. A., Donelson, J. M. et al. (2012) Parental environment mediates impacts of increased carbon dioxide on a coral reef fish. Nat. Clim. Change, 2, 858-861
23. Mitra, A., Castellani, C., Gentleman, W. et al. (2014) Bridging the gap between marine biogeochemical and fisheries sciences; configuring the zooplankton link. Prog. Oceanogr., doi:10.1016/j.pocean.2014.04.025
24. Morita, M., Suwa, R., Iguchi, A et al. (2010) Ocean acidification reduces sperm flagellar motility. Zygote, 18, 1-5
25. Niehoff, B. (2007) Life history strategies in zooplankton communities: The significance of female gonad morphology and maturation types for the reproductive biology of marine calanoid copepods. Prog. Oceanogr., 74, 1-47
26. Parker, L. M., Ross, P. M., O'Connor, W. A. et al. (2012) Adult exposure influences offspring response to ocean acidification in oysters. Global Change Biol., 18, 82-92
27. Parrish, K. K. and Wilson, D. F. (1978) Fecundity studies on Acartia tonsa (Copepoda: Calanoida) in standardized culture. Mar. Biol., 46, 65-81
28. Pierrot, D., Lewis, E. and Wallace, D. W. R. (2006) CO2sys MS Excel Program Developed for CO2 System Calculations. ORNL/CDIAC-105. Carbon Dioxide Information Analysis Center, Oak Ridge National Laboratory, US Department of Energy, Oak Ridge, TN.
29. Pond, D., Harris, R., Head, R. et al. (1996) Environmental and nutritional factors determining seasonal variability in the fecundity and egg viability of Calanus helgolandicus in coastal waters off Plymouth, UK. Mar. Ecol. Prog. Ser., 143, 45-63
30. Reuter, K. E., Lotterhos, K. E., Crim, R. N. et al. (2011) Elevated pCO2 increases sperm limitation and risk of polyspermy in the red sea urchin Strongylocenttrotus franciascanus. Global Change Biol., 17, 163-171
31. Riebesell, U., Fabry, V. J., Hansson, L. et al. (Eds.) (2010) Guide to best practices for ocean acidification research and data reporting. Publications Office of the European Union, Luxembourg, 260p.
32. Rossoll, D., Bermúdez, R., Hauss, H. et al. (2012) Ocean acidificationinduced food quality deterioration constrains trophic transfer. PLoS ONE, 7, e34737
33. Sedlacek, C. (2008) The biochemical composition of naupii derived from stored non-diapause and diapause copepod eggs and the biology of diapausing eggs. Electronic Theses, Treatises and Dissertations. http://diginole.lib. fsu.edu/etd/283
34. Sichlau, H. M. and Kiorboe, T. (2011) Age- and size- dependent mating performance and fertility in a pelagic copepod, Temora longicornis. Mar. Ecol. Prog. Ser., 442, 147-153
35. Titelman, J., Varpe, O., Eliassen, S. et al. (2007) Copepod mating: chance or choice?. J. Plankton. Res., 29, 1023-1030
36. Vihtakari, M., Hendricjs, I E., Holding, J. et al. (2013) Effects of ocean acidification and warming on sperm activity and early life stages of the Mediterranean mussel (Mytilus galloprovincialis).Water, 5, 1890-1915
37. Vuuren, D. P., Edmonds, J., Kainuma, M. et al. (2011) The representative concentration pathways: An overview. Clim. Change, 109, 5-31