全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

The Impacts of Ex Situ Transplantation on the Physiology of the Taiwanese Reef-Building Coral Seriatopora hystrix

DOI: 10.1155/2013/569361

Full-Text   Cite this paper   Add to My Lib

Abstract:

We sought to determine whether the Indo-Pacific reef-building coral Seriatopora hystrix performs in a similar manner in the laboratory as it does in situ by measuring Symbiodinium density, chlorophyll a (chl-a) concentration, and the maximum quantum yield of photosystem II ( ) at the time of field sampling (in situ), as well as after three weeks of acclimation and one week of experimentation (ex situ). Symbiodinium density was similar between corals of the two study sites, Houbihu (an upwelling reef) and Houwan (a nonupwelling reef), and also remained at similar levels ex situ as in situ. On the other hand, both areal and cell-specific chl-a concentrations approximately doubled ex situ relative to in situ, an increase that may be due to having employed a light regime that differed from that experienced by these corals on the reefs of southern Taiwan from which they were collected. As this change in Symbiodinium chl-a content was documented in corals of both sites, the experiment itself was not biased by this difference. Furthermore, increased by only 1% ex situ relative to in situ, indicating that the corals maintained a similar level of photosynthetic performance as displayed in situ even after one month in captivity. 1. Introduction Molecular biology promises to yield insight into the subcellular mechanisms underlying the stable mutualism between reef-building scleractinians and dinoflagellates of the genus Symbiodinium [1, 2], as well as their macromolecular responses to changes in their environment [3–5]. The latter topic is of particular interest given that global climate change (GCC)-driven temperature and pCO2 increases have been hypothesized to lead to more frequent coral bleaching events in the years to come [6]. Alongside other anthropogenic pressures, such GCC-derived threats have generated an urgent need to shift the monitoring of coral reef health from a retroactive process to a proactive one [7]. Assessment of reef health is currently conducted by visual surveys in which the number of dying or dead corals is quantified (e.g., [8]). However, such late-stage manifestations of health decline likely occurred well after the initial insult. An analysis of the expression or activity of subcellular biomarkers, such as stress genes and proteins, may allow for the determination of which corals are at risk from anthropogenic impacts on a proactive timescale. Such a monitoring approach could potentially allow for scientists and managers to work together to mitigate local-scale insults to reef stability, such as water pollution [9], prior to extensive

References

[1]  S. E. Peng, W. N. U. Chen, H. K. Chen et al., “Lipid bodies in coral-dinoflagellate endosymbiosis: proteomic and ultrastructural studies,” Proteomics, vol. 11, no. 17, pp. 3540–3555, 2011.
[2]  W. N. U. Chen, H. J. Kang, V. M. Weis et al., “Diel rhythmicity of lipid-body formation in a coral-Symbiodinium endosymbiosis,” Coral Reefs, vol. 31, no. 2, pp. 521–534, 2012.
[3]  A. B. Mayfield, L. H. Wang, P. C. Tang et al., “Assessing the impacts of experimentally elevated temperature on the biological composition and molecular chaperone gene expression of a reef coral,” PLoS ONE, vol. 6, no. 10, article e26529, 2011.
[4]  A. B. Mayfield, P. H. Chan, H. M. Putnam, C. S. Chen, and T. Y. Fan, “The effects of a variable temperature regime on the physiology of the reef-building coral Seriatopora hystrix: results from a laboratory-based reciprocal transplant,” The Journal of Experimental Biology, vol. 215, pp. 4183–4195, 2012.
[5]  A. B. Mayfield, M. N. Chen, P. J. Meng, H. J. Lin, C. S. Chen, and P. J. Liu, “The physiological response of the reef coral Pocillopora damicornis to elevated temperature: results from coral reef mesocosm experiments in Southern Taiwan,” Marine Environmental Research, vol. 86, pp. 1–11, 2013.
[6]  O. Hoegh-Guldberg, P. J. Mumby, A. J. Hooten et al., “Coral reefs under rapid climate change and ocean acidification,” Science, vol. 318, no. 5857, pp. 1737–1742, 2007.
[7]  M. J. H. van Oppen and R. D. Gates, “Conservation genetics and the resilience of reef-building corals,” Molecular Ecology, vol. 15, no. 13, pp. 3863–3883, 2006.
[8]  J. R. Guest, A. H. Baird, J. A. Maynard et al., “Contrasting patterns of coral bleaching susceptibility in 2010 suggest an adaptive response to thermal stress,” PLoS ONE, vol. 7, no. 3, article e33353, 2012.
[9]  C. A. Downs, E. Mueller, S. Phillips, J. E. Fauth, and C. M. Woodley, “A molecular biomarker system for assessing the health of coral (Montastraea faveolata) during heat stress,” Marine Biotechnology, vol. 2, no. 6, pp. 533–544, 2000.
[10]  D. J. Barshis, J. H. Stillman, R. D. Gates, R. J. Toonen, L. W. Smith, and C. Birkeland, “Protein expression and genetic structure of the coral Porites lobata in an environmentally extreme Samoan back reef: does host genotype limit phenotypic plasticity?” Molecular Ecology, vol. 19, no. 8, pp. 1705–1720, 2010.
[11]  D. J. Barshis, J. T. Ladner, T. A. Oliver, F. O. Seneca, N. Traylor-Knowles, and S. R. Palumbi, “Genomic basis for coral resilience to climate change,” Proceedings of the National Academy of Sciences of the United States of America, vol. 110, pp. 1387–1392, 2013.
[12]  M. K. Desalvo, C. R. Voolstra, S. Sunagawa et al., “Differential gene expression during thermal stress and bleaching in the Caribbean coral Montastraea faveolata,” Molecular Ecology, vol. 17, no. 17, pp. 3952–3971, 2008.
[13]  H. M. Putnam, A. B. Mayfield, T. Y. Fan, C. S. Chen, and R. D. Gates, “The physiological and molecular responses of larvae from the reef-building coral Pocillopora damicornis exposed to near-future increases in temperature and pCO2,” Marine Biology, vol. 160, no. 8, pp. 2157–2173, 2013.
[14]  C. A. Downs, J. E. Fauth, C. E. Robinson et al., “Cellular diagnostics and coral health: declining coral health in the Florida Keys,” Marine Pollution Bulletin, vol. 51, no. 5–7, pp. 558–569, 2005.
[15]  A. Crawley, D. I. Kline, S. Dunn, K. Anthony, and S. Dove, “The effect of ocean acidification on symbiont photorespiration and productivity in Acropora formosa,” Global Change Biology, vol. 16, no. 2, pp. 851–863, 2010.
[16]  D. Tchernov, H. Kvitt, L. Haramaty et al., “Apoptosis and the selective survival of host animals following thermal bleaching in zooxanthellate corals,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 24, pp. 9905–9909, 2011.
[17]  S. Jan and C. T. A. Chen, “Potential biogeochemical effects from vigorous internal tides generated in Luzon Strait: a case study at the southernmost coast of Taiwan,” Journal of Geophysical Research, vol. 114, no. 4, 2009.
[18]  W. K. Fitt, R. D. Gates, O. Hoegh-Guldberg et al., “Response of two species of Indo-Pacific corals, Porites cylindrica and Stylophora pistillata, to short-term thermal stress: the host does matter in determining the tolerance of corals to bleaching,” Journal of Experimental Marine Biology and Ecology, vol. 373, no. 2, pp. 102–110, 2009.
[19]  J. Stimson and R. A. Kinzie III, “The temporal pattern and rate of release of zooxanthellae from the reef coral Pocillopora damicornis (Linnaeus) under nitrogen-enrichment and control conditions,” Journal of Experimental Marine Biology and Ecology, vol. 153, no. 1, pp. 63–74, 1991.
[20]  A. B. Mayfield, T. Y. Fan, and C. S. Chen, “Physiological acclimation to elevated temperature in a reef-building coral from an upwelling environment,” Coral Reefs, 2013.
[21]  A. B. Mayfield, M. B. Hirst, and R. D. Gates, “Gene expression normalization in a dual-compartment system: a real-time quantitative polymerase chain reaction protocol for symbiotic anthozoans,” Molecular Ecology Resources, vol. 9, no. 2, pp. 462–470, 2009.
[22]  A. B. Mayfield, Y. Y. Hsiao, T. Y. Fan, and C. S. Chen, “Temporal variation in RNA/DNA and protein/DNA ratios in four anthozoan-dinoflagellate endosymbioses of the Indo-Pacific: implications for molecular diagnostics,” Platax, vol. 16, pp. 29–52, 2012.
[23]  A. B. Mayfield, Y. Y. Hsiao, T. Y. Fan, C. S. Chen, and R. D. Gates, “Evaluating the temporal stability of stress-activated protein kinase and cytoskeleton gene expression in the Pacific reef corals Pocillopora damicornis and Seriatopora hystrix,” Journal of Experimental Marine Biology and Ecology, vol. 395, no. 1-2, pp. 215–222, 2010.
[24]  V. R. Cumbo, T. Y. Fan, and P. J. Edmunds, “Physiological development of brooded larvae from two pocilloporid corals in Taiwan,” Marine Biology, 2013.
[25]  I. Yakovleva and M. Hidaka, “Differential recovery of PSII function and electron transport rate in symbiotic dinoflagellates as a possible determinant of bleaching susceptibility of corals,” Marine Ecology Progress Series, vol. 268, pp. 43–53, 2004.
[26]  P. G. Falkowski and J. A. Raven, Aquatic Photosynthesis, Princeton University Press, Princeton, NJ, USA, 2007.
[27]  Y. Loya, K. Sakai, K. Yamazato, Y. Nakano, H. Sambali, and R. van Woesik, “Coral bleaching: the winners and the losers,” Ecology Letters, vol. 4, no. 2, pp. 122–131, 2001.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413