Academic literature on the topic 'Seriatopora hystrix'

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Journal articles on the topic "Seriatopora hystrix"

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Maier, E., A. Buckenmaier, R. Tollrian, and B. Nürnberger. "Intracolonial genetic variation in the scleractinian coral Seriatopora hystrix." Coral Reefs 31, no. 2 (December 15, 2011): 505–17. http://dx.doi.org/10.1007/s00338-011-0857-9.

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Sherman, C. D. H. "Mating system variation in the hermaphroditic brooding coral, Seriatopora hystrix." Heredity 100, no. 3 (November 7, 2007): 296–303. http://dx.doi.org/10.1038/sj.hdy.6801076.

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Rädecker, N., FW Meyer, VN Bednarz, U. Cardini, and C. Wild. "Ocean acidification rapidly reduces dinitrogen fixation associated with the hermatypic coral Seriatopora hystrix." Marine Ecology Progress Series 511 (September 24, 2014): 297–302. http://dx.doi.org/10.3354/meps10912.

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Pantos, Olga, Pim Bongaerts, Paul G. Dennis, Gene W. Tyson, and Ove Hoegh-Guldberg. "Habitat-specific environmental conditions primarily control the microbiomes of the coral Seriatopora hystrix." ISME Journal 9, no. 9 (February 10, 2015): 1916–27. http://dx.doi.org/10.1038/ismej.2015.3.

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Frederic Sinniger, Masaya Morita, and Saki Harii. "“Locally extinct” coral species Seriatopora hystrix found at upper mesophotic depths in Okinawa." Coral Reefs 32, no. 1 (October 26, 2012): 153. http://dx.doi.org/10.1007/s00338-012-0973-1.

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Maier, Elke, Ralph Tollrian, Baruch Rinkevich, and Beate Nürnberger. "Isolation by distance in the scleractinian coral Seriatopora hystrix from the Red Sea." Marine Biology 147, no. 5 (July 21, 2005): 1109–20. http://dx.doi.org/10.1007/s00227-005-0013-6.

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Cooper, Timothy F., Karin E. Ulstrup, Sana S. Dandan, Andrew J. Heyward, Michael Kühl, Andrew Muirhead, Rebecca A. O'Leary, Bibi E. F. Ziersen, and Madeleine J. H. Van Oppen. "Niche specialization of reef-building corals in the mesophotic zone: metabolic trade-offs between divergent Symbiodinium types." Proceedings of the Royal Society B: Biological Sciences 278, no. 1713 (November 24, 2010): 1840–50. http://dx.doi.org/10.1098/rspb.2010.2321.

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The photobiology of two reef corals and the distribution of associated symbiont types were investigated over a depth gradient of 0–60 m at Scott Reef, Western Australia. Pachyseris speciosa hosted mainly the same Symbiodinium C type similar to C3 irrespective of sampling depth. By contrast, Seriatopora hystrix hosted predominantly Symbiodinium type D1a or D1a-like at shallow depths while those in deeper water were dominated by a Symbiodinium C type closely related to C1. The photosynthesis/respiration (P/R) ratio increased consistently with depth at the two sampling times (November 2008 and April 2009) for P. speciosa and in November 2008 only for S. hystrix , suggesting a reduction in metabolic energy expended for every unit of energy obtained from photosynthesis. However, in April 2009, shallow colonies of S. hystrix exhibited decreased P/R ratios down to depths of approximately 23 m, below which the ratio increased towards the maximum depth sampled. This pattern was mirrored by changes in tissue biomass determined as total protein content. The depth of change in the direction of the P/R ratio correlated with a shift from Symbiodinium D to C-dominated colonies. We conclude that while photobiological flexibility is vital for persistence in contrasting light regimes, a shift in Symbiodinium type may also confer a functional advantage albeit at a metabolic cost with increased depth.
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Bongaerts, Pim, Cynthia Riginos, Tyrone Ridgway, Eugenia M. Sampayo, Madeleine J. H. van Oppen, Norbert Englebert, Francisca Vermeulen, and Ove Hoegh-Guldberg. "Genetic Divergence across Habitats in the Widespread Coral Seriatopora hystrix and Its Associated Symbiodinium." PLoS ONE 5, no. 5 (May 27, 2010): e10871. http://dx.doi.org/10.1371/journal.pone.0010871.

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Muko, Soyoka, Seiji Arakaki, Reiko Tamai, and Kazuhiko Sakai. "An individual-based model for population viability analysis of the brooding coral Seriatopora hystrix." Ecological Modelling 277 (April 2014): 68–76. http://dx.doi.org/10.1016/j.ecolmodel.2014.01.025.

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Prasetia, Rian, Frederic Sinniger, Kaito Hashizume, and Saki Harii. "Reproductive biology of the deep brooding coral Seriatopora hystrix: Implications for shallow reef recovery." PLOS ONE 12, no. 5 (May 16, 2017): e0177034. http://dx.doi.org/10.1371/journal.pone.0177034.

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Dissertations / Theses on the topic "Seriatopora hystrix"

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Maier, Elke. "Life history of the Scleractinian Coral Seriatopora hystrix." Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-149063.

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Maier, Elke [Verfasser], and Beate [Akademischer Betreuer] Nürnberger. "Life history of the Scleractinian Coral Seriatopora hystrix : a population genetic approach / Elke Maier. Betreuer: Beate Nürnberger." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2010. http://d-nb.info/1026846781/34.

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Underwood, Jim. "Routine and rare genetic connections in corals off northwest Australia and the implications for conservation." University of Western Australia. School of Animal Biology, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0158.

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[Truncated abstract] The extent to which marine populations are connected by larval dispersal is crucial to their distribution, maintenance and diversity. Thus, for the effective conservation of threatened systems such as coral reefs, understanding patterns of connectivity is essential. However, the biophysical mechanisms that retain or disperse larvae within and among populations are poorly understood. Though the open ocean environment provides the opportunity for long-distance dispersal, if this potential is only rarely realised, recruits produced from afar are unlikely to contribute to the local-scale demography of populations over ecological time frames, but will limit broad-scale genetic diversification over evolutionary time. This thesis explores the extent of genetic and demographic connectivity of two species of reef-building corals over a range of spatial scales among the discontinuous reef systems of northwest Australia. ... Putative source and sink dynamics were not random, but were associated with levels of disturbance and recovery from a recent and catastrophic coral bleaching. When S. hystrix samples from another two offshore systems were included in the analysis, large differences among systems showed that gene flow over hundreds of kilometres is rare over microevolutionary time scales that account for connections over multiple generations. Levels of subdivision over the same spatial scales were markedly lower in the acroporid coral, Acropora tenuis, than in S. hystrix. These results are congruent with expectations based on reproductive mode; in contrast to S. hystrix, which releases brooded larvae that are competent to settle immediately, A. tenuis broadcasts its gametes, and after external fertilisation, the larvae need to develop for several days before they are competent to settle. Despite the differences in levels of broad-scale subdivision, in both species significant differentiation was detected between reefs within systems (>10 km), and between sites within some reefs (< 10 km). These results indicate not only that dispersal between reefs and even some reef patches is restricted, but also that hydrodynamics influence retention of brooded and spawned larvae in similar ways. Further analysis of A. tenuis populations from two coastal systems detected significant differences in genetic diversity among the four major systems of northwest Australia. Additionally, genetic divergence between the coastal and offshore zones was greater than expected by the geographic separation of systems, indicating that connectivity between these zones via transport of A. tenuis larvae on oceanic currents occurs rarely even over microevolutionary time scales. This study has two primary implications for conservation. First, since coastal and offshore reefs of northwest Australia appear to be discrete genetic entities, they have independent evolutionary potential to adapt to local conditions and environmental change. Second, systems, reefs and some reef patches of northwest Australia are demographically independent units. Therefore, designs of coral reserve networks should consider routine dispersal distances of kilometres to a few tens of kilometres.
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Chen, Yi-Hsuan, and 陳宜暄. "Genetic Structure of Seriatopora hystrix Populations in Different Geographic Scales." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/83281213167746873515.

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碩士
國立臺灣大學
海洋研究所
102
It has been hypothesized that the isolation-by-distance effect and ecological selection could lead to high level of population subdivision in different spatial scales. Here we investigated the genetic diversity and genetic structure of a common brooding coral Seriatopora hystrix in various geographic scales in Taiwan by using 6 microsatellite markers. Totally, 285 samples were collected from 7 sites including Taiping Island in the South China Sea, the outlet of the Third Nuclear Power Plant, Tiaoshi and Jialeshuei in Kenting National Park, Lanyu and Sanxiantai in Taitung County, and Tofujia in Yilan County. Our results showed that the population of Taiping Island had higher genetic diversity and two unique genetic clusters could be identified. Significant genetic differentiation was detected among all populations at both small (3~25 km) and large (> 1700 km) geographic scales, and this pattern was not associated with geographic distance (r2 = 0.030, p = 0.705). This study demonstrates that the isolation-by-distance effect may be modified by ecological selection or interactions between environmental factors and life history traits.
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Chan, Pei-Hsun, and 詹珮熏. "Effects of stable and variable temperature on the physiological performance of the reef coral, Seriatopora hystrix." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/96259456505975210810.

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碩士
國立東華大學
海洋生物多樣性及演化研究所
98
The majority of research on the response of corals to temperature has been conducted with consideration to stable temperatures. Although studies show that seawater temperature can be highly variable on coral reefs, much is still unknown about the physiological response of coral to temperature fluctuations. In NanWan Bay, southern Taiwan, temperature variation due to upwelling by internal tides is common, and seawater temperature can change as much as 3 - 10 °C in a 24h period in summer. In contrast, on the west coast of Taiwan, where there is no upwelling, and temperature is relatively stable. In order to examine the effects of stable and fluctuating temperatures on coral from different physical environments, we completed a one-week manipulative temperature experiment using the common brooding coral, Seriatopora hystrix, from two different environments of Houbihu (NanWan Bay) and Houwan (West Coast). Corals were either exposed to a stable (26 °C) or fluctuating temperature (23 – 29 °C, within 24h) treatments. Following seven days of treatment, we measured physiological parameters to understand the effect of the different temperature environments on experimental corals. Coral tissue color, zooxanthellae density and Photosystem II photochemical efficiency did not change substantially in comparison to initial values. When comparing between sites and treatments, the concentration of chlorophyll-a changed significantly in the treatments depending on the original environment of coral collection. Specifically, the response of Houwan corals was higher in stable treatments in comparison to variable, and the opposite was true for Houbihu corals, which had higher chlorophyll-a in the variable treatments. Even though there were no significant differences of the main effects on coral growth rate, there was a significant interaction, similarly to the response of chlorophyll-a. Together, these results suggest the primary response of corals to temperature was a change in the concentration of chlorophyll-a when the thermal environment changed. The response of corals to the temperature treatments revealed higher chlorophyll-a and growth rate in the treatment most similar to their original environment, suggesting local environmental acclimatization or adaptation.
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Hsieh, Yu-Chieh, and 謝語婕. "Inter-annual variation of lunar periodicity in larval release by reef corals Pocillopora damicornis and Seriatopora hystrix." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/22363624049933141250.

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碩士
國立東華大學
海洋生物多樣性及演化研究所
97
In this study, we describe inter-annual variation of larval release by two brooding reef corals, Pocillopora damicornis and Seriatopora hystrix in Southern Taiwan. Corals were collected from shallow locations in Nanwan Bay and maintained in outdoor, flow-through systems to quantify and record daily larval release. The mean lunar day representing the peak of larval release cycle was analyzed by circular statistics, and then regression between the mean lunar day and monthly mean seawater temperature was examined. P. damicornis and S. hystrix showed similar patterns of tight synchronization with respect to the lunar phase, but importantly, the phase of this synchronization shifted in a predictable pattern between seasons. In 2003, 2005 and 2008, the mean lunar day for larval release occurred around the full moon phase and spring tide in winter then shifted to the first quarter moon phase and neap tide in summer. The mean lunar day for larval release was significantly negatively regressed with mean seawater temperature. In Nanwan Bay, the tidally-induced upwelling and corresponding rapid and large temperature changes in spring tide provide the possible explanation why larval release timing shift to neap tide in summer. However, there was not a significant regression from lunar January to June in 2007. Notably, the mean lunar day ( 8.6- 9.6 ) of larval release in February and March was earlier in 2007 than those ( 11.5- 19.3 ) in previous years, and the mean monthly seawater temperature from November 2006 to February 2007 was significantly warmer ( 1.1- 2.8℃ ) than those during the winters of 2003 and 2005. The results suggest that higher seawater temperature may drive early larval release, possibly by reducing the development time of gametes and embryos. These results are important as they suggest that coral reproductive timing may be influenced by rising temperatures associated climate change.
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7

Ya-Hsuan, Tung, and 童亞瑄. "Temperature effects on the growth and survival of reef corals Stylophora pistillata and Seriatopora hystrix: A mesocosm study." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/uxm2m5.

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碩士
國立臺灣大學
海洋研究所
92
The purpose of this study is to compare the effects of sea temperature on growth rate and mortality of reef corals, Stylophora pistillata and Seriatopora hystrix. Coral colonies were collected from Nanwan Bay, southern Taiwan. Coral branches were prepared and cultured in mesocosms at three temperature regimes (28, 25 and 20℃, each 2 replicates). The growth of corals was measured at three-week intervals by a buoyant weighting technique. The mean growth rates of S. pistillata and S. hystrix at 25℃(S. pistillata: 0.0126±0.0045 g/g*day; S. hystrix: 0.0253±0.0081 g/g*day) were significantly higher than those at 28℃(S. pistillata: 0.0066±0.0027 g/g*day; S. hystrix: 0.0083±0.0046 g/g*day) and 20℃(S. pistillata: 0.0058±0.0014 g/g*day; S. hystrix: 0.0047±0.0022 g/g*day).The mean growth rates of S. hystrix in two mesocosms at 25℃ were similar and significantly higher than those of S. pistillata. However, the mean growth rates of S. pistillata in two mesocosms at 25℃ were significantly different. The mean growth rates of S. hystrix in two mesocosms at 28℃ were significantly different and did not show a consistant relationship compared to those of S. pistillata. The mean growth rates of S. hystrix in two mesocosms at 20℃ were significantly different, but those of S. pistillata were the same. This suggests that the effects of temperature on growth of the two coral species were different. Growth rates of S. hystrix at 25℃ were stable and higher than those of S. pistillata. However, the effects of temperature on growth rate of S. hystrix may be modified by other factors (e.g., mesocosm effect) in higher or lower temperatures. The mortality of S. pistillata in three temperature treatments was very low, while the partial mortality of S. hystrix at 28℃ (37.5 %) was significantly higher than that at 25 (2.1 %) and 20℃ (2.1 %). This suggests that S. hystrix is more sensitive and vulnerable to high sea temperatures.
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