Corals are able to source autotrophically-produced carbon since they have symbiotic unicellular dinoflagellates embedded in their tissue. However, they are also known to be heterotrophic feeders and able to ingest a variety of food sources, such as bacteria, particulate organic matter and zooplankton. Recent research has shown that heterotrophic feeding has a marked effect on both maintenance and growth in corals by providing mainly a nutritional source of nitrogen and phosphorus. Nevertheless, no study has yet been undertaken on the interactions between feeding and sexual reproduction in corals. This study examines the effects of heterotrophic feeding on the sexual reproduction of Pocillopora verrucosa in aquaria. Rotifers were used as live food source at two concentrations (LFC = low feed colonies) = 5×102 organisms/L; (HFC = high feed colonies) = 15×102 organisms /L) and an unfed control (UC = unfed colonies) was added for comparison. Three replicates of five colonies were used for each food concentration and control. Rotifers were distributed among the nine aquaria four times per week for three hours. Histological sections of coral polyps were prepared to monitor the development of gametogenic stages and the fecundity of the colonies. The number and size of oocyte, and spermary stages were determined in each polyp. Both fed and starved colonies proved to be simultaneous hermaphrodites and broadcast spawners. The gametogenesis period was short and occurred from October to December 2007. No spawning event was observed in the aquaria. However, the disappearance of mature oocytes in samples collected in January 2008 suggested that spawning took place between December 2007 and January 2008. Heterotrophic feeding had a strong effect on reproduction in P.verrucosa. The results showed that both the proportion of polyps with gametes and the reproductive effort were lower in the fed than in starved colonies. It is likely that an energetic trade-off occurred between reproduction and other metabolic functions. However, oocytes were bigger in fed corals compared with the unfed controls. Several hypotheses are proposed to explain these metabolic/energy distribution patterns. / Thesis (M.Sc.)-University of KwaZulu-Natal, Westville, 2009.

Thesis (Ph.D.) -- James Cook University, 1998. / Typescript (photocopy) Bibliography: leaves 110-118.

Biodiversity of coral reefs is higher than in any other marine ecosystem, and significant research has focused on studying coral taxonomy, physiology, ecology, and coral-associated fauna. Yet little is known about symbiotic copepods, abundant and numerous microscopic crustaceans inhabiting almost every living coral colony. In this thesis, I investigate the genetic diversity of different groups of copepods associated with reef-building corals in distinct parts of the Indo-Pacific; determine species boundaries; and reveal patterns of biogeography, endemism, and host-specificity in these symbiotic systems. A non-destructive method of DNA extraction allowed me to use an integrated approach to conduct a diversity assessment of different groups of copepods and to determine species boundaries using molecular and taxonomical methods. Overall, for this thesis, I processed and analyzed 1850 copepod specimens, representing 269 MOTUs collected from 125 colonies of 43 species of scleractinian corals from 11 locations in the Indo-Pacific. The genetic assessment of the most abundant copepod morphotypes associated with hermatypic corals in Lizard Island (Great Barrier Reef) revealed a large number of species previously unknown for this region. Analyses of diversity and patterns of biogeographical distribution of copepods associated with Galaxea corals throughout the Indo-Pacific showed that the species diversity of this group is high and appears to be regionally specific, an uncommon pattern in most coral reef-associated invertebrates. Results for the symbiotic copepod fauna of Red Sea pocilloporid corals, a family of corals with a high level of morphological variability within and among its members, showed that the majority of the discovered poecilostomatoid copepods belong to the genus Spaniomolgus, which demonstrated a significant genetic diversity of morphologically-similar species. Assessment of the diversity of copepods associated with the Red Sea mushroom corals revealed several undescribed species and showed no evidence of specificity to the hosts neither on species nor on the family level, which contradicts a modern assumption of high host-specificity of copepods. Overall, this dissertation is a first study of genetic diversity of copepods associated with invertebrates, and it provides substantial insight into the diversity of coral-associated microcrustaceans and insight to patterns of their host-specificity as well as distribution around the Indo-Pacific.

Uma das espécies de coral pétreo zooxantelado com mais ampla distribuição no litoral brasileiro é Madracis decactis Lyman, 1859. M. decactis forma colônias incrustantes nodulares que podem atingir até 30 cm de diâmetro. O estudo da gametogênese foi realizado através de coletas bimensais na Baía de Ilha Grande, RJ durante 21 meses (agosto/2004-maio/2006), totalizando 10 coletas (12 colônias/coleta) (Licença IBAMA no. 201/2004). Foram realizados cortes histológicos de 7 µm, e de 10 até 16 pólipos por colônia foram analisados, totalizando mais de 1800 pólipos. A análise dos pólipos indicou que M. decactis é hermafrodita, com gametas localizados no mesmo lóculo gástrico, porém em mesentérios diferentes. A gametogênese durou cerca de sete meses. A ovogênese iniciou-se ao redor de outubro, enquanto que a espermatogênese teve inicio no final de fevereiro, ambas terminando em sincronia no final do mês de maio. O exame dos pólipos férteis indicou a presença dos estágios I, II e III de desenvolvimento para a ovogênese e dos estágios I, II, III e IV para a espermatogênese. Não foram encontrados embriões ou plânulas nos cortes histológicos, indicando talvez que estes estágios permaneçam pouco tempo no interior do pólipo. O pico da atividade reprodutiva ocorre entre os meses de fevereiro e abril com todas as colônias férteis contendo ovócitos principalmente no estágio III de maturação. A provável época de liberação de plânulas ocorre entre os meses de abril e maio, sob influencia das condições ambientais como a temperatura da água do mar, a irradiação solar e a pluviosidade. O presente trabalho forneceu informações básicas a respeito da biologia reprodutiva de Madracis decactis presente em Ilha Grande, sendo uma contribuição para outros estudos mais específicos na área de manejo e conservação de ambientes marinhos. / One of the most wide distributed coral species along the Brazilian cost is Madracis decactis Lyman, 1859. M. decactis growths as nodular incrusting colonies that can reach up to 30 cm in diameter. In order to study the gametogenesis cycle, bimonthly collections were done at Ilha Grande Bay, Rio de Janeiro, during 21 months (August/2004- May/2006), totaling 10 collections (12 colonies/collection) (License no. 201/2004). Histological sections of 7 µm thick were done to analyze 10 to 16 polyps per colony (more than 1800 polyps in total). The analysis indicated that M. decactis is hermaphroditic, with male and female gametes developing at the same gastric loculi, but in different mesenteries. The gametogenesis lasted about 7 months, the oogenesis starts at October , while spermtogenesis starts at the end of February, both reaching the maturity in synchrony at the end of May. The exam of fertile polyps indicated the presence of stages I, II and III for oogenesis and I, II, III and IV for spermatogenesis. No embryo or planula were observed in the histological sections, indicating that maybe these stages stay for a short period inside the polyp cavity. The peak of reproductive activity was between February and April when all the polyps were fertile containing manly stage III oocytes. The releasing of planulae may happen between April and May, under the influence of environmental conditions as sea water temperature, solar insolation and rainy season. The present study has provided basic information about the reproductive biology of Madracis decactis from Ilha Grande Bay, and it may be a contribution to further studies about management and conservation of marine environments.

Very little is known about the association between Symbiodinium dinoflagellates, which perform the majority of primary production in coral reefs, and metazoan larvae. This thesis performed three experiments on the association between Symbiodinium and Mussismilia hispida (coral), Berghia stephanieae (nudibranch) and Tridacna crocea (giant clam) larvae. The first experiment monitored the expression of a symbiosis-specific gene in Symbiodinium clade A associated with the three larval forms during a 72-h window. The second experiment quantified the production of symbiosis-related ω3 fatty acids in Symbiodinium clades A-F also associated with the three larval hosts and the third experiment verified bleaching rates at 26, 29 and 32ºC in the larvae associated with clades A-F. The main results show that i) a symbiosis-specific gene is expressed by Symbiodinium A associated with M. hispida and T. crocea larvae, but not with B. stephanieae; ii) the DHA fatty acid is produced in significantly higher amounts by clades A and C associated with M. hispida and T. crocea larvae; and iii) that M. hispida and T. crocea larvae associated with Symbiodinium A and C have significantly lower bleaching rates. These findings suggest that clades A and C establish a more robust mutualism with M. hispida and T. crocea larvae, but there seems to be no mutualism between Symbiodinium and B. stephanieae. / Muito pouco é conhecido sobre a associação entre dinoflagelados do gênero Symbiodinium e larvas de metazoários. Essa tese realizou três experimentos sobre a associação entre Symbiodinium e larvas de Mussismilia hispida (coral), Berghia stephanieae (nudibrânquio) e Tridacna crocea (vieira gigante). O primeiro experimento verificou a expressão de um gene específico para a relação simbiótica em Symbiodinium A associado com as larvas dos três hospedeiros. O segundo experimento quantificou a produção de ácidos graxos nos clados A-F de Symbiodinium também associados com as larvas dos três hospedeiros; o terceiro monitorou a perda de simbiontes nos três tipos larvais associados com os clados A-F, em temperaturas de 26, 29 e 32ºC. Os principais resultados mostram que: i) um gene específico para a simbiose é expresso por Symbiodinium A associado com M. hispida e T. crocea, mas não com B. stephanieae; ii) o ácido graxo DHA é produzido em quantidades significantemente maiores pelos clados A e C associados com M. hispida e T. crocea; e iii) M. hispida e T. crocea associadas com Symbiodinium A e C possuem taxas de perda de simbiontes significantemente menores do que os demais. Esses resultados mostram que os clados A e C estabelecem um mutualismo mais robusto com M. hispida e T. crocea, mas não há relação mutualística entre Symbiodinium e B. stephanieae.

Ma Wai Chun. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2005. / Includes bibliographical references (leaves 135-150). / Abstracts in English and Chinese. / Acknowledgements --- p.i / Abstract --- p.iii / 論文摘要 --- p.vii / Table of contents --- p.x / List of table --- p.xii / List of figure --- p.xiii / Chapter Chapter 1 --- General introduction --- p.1 / Chapter 1.1 --- Studies on coral population dynamics --- p.1 / Chapter 1.2 --- The study site --- p.5 / Chapter 1.3 --- The experimental organisms --- p.7 / Chapter 1.4 --- Objectives --- p.8 / Chapter 1.5 --- Outline of the thesis --- p.9 / Chapter Chapter 2 --- The patterns of recruitment and mortality of Oulastrea crispata --- p.13 / Chapter 2.1 --- Introduction --- p.13 / Chapter 2.1.1 --- Recruitment --- p.13 / Chapter 2.1.2 --- Colony mortality --- p.16 / Chapter 2.1.3 --- Studies on coral recruitment and mortality in Hong Kong --- p.18 / Chapter 2.2 --- Material & methods --- p.20 / Chapter 2.2.1 --- Sampling methods --- p.20 / Chapter 2.2.2 --- Data and statistical analysis --- p.22 / Chapter 2.3 --- Results --- p.23 / Chapter 2.3.1 --- Recruitment patterns --- p.23 / Chapter 2.3.2 --- Mortality patterns --- p.26 / Chapter 2.4 --- Discussion --- p.29 / Chapter 2.4.1 --- Recruitment --- p.29 / Chapter 2.4.2 --- Mortality --- p.33 / Chapter Chapter 3 --- The growth and population structure of a scleractinian coral Oulastrea crispata --- p.58 / Chapter 3.1 --- Introduction --- p.58 / Chapter 3.2 --- Materials & methods --- p.66 / Chapter 3.2.1 --- Field procedures --- p.66 / Chapter 3.2.2 --- Laboratory procedures --- p.67 / Chapter 3.2.3 --- Data analysis --- p.67 / Chapter 3.3 --- Results --- p.68 / Chapter 3.4 --- Discussion --- p.73 / Chapter 3.4.1 --- The mode of budding for Oulastrea --- p.73 / Chapter 3.4.2 --- The methods of measurement --- p.74 / Chapter 3.4.3 --- The limitation in searching for new recruits --- p.78 / Chapter 3.4.4 --- The variation in the growth curves of Oulastrea --- p.78 / Chapter 3.4.5 --- The seasonal changes in growth rates --- p.79 / Chapter 3.4.6 --- The variation of size structures --- p.81 / Chapter 3.4.7 --- Conclusions --- p.82 / Chapter Chapter 4 --- The competition between a scleractinian coral Oulastrea crispata and macroalgae --- p.109 / Chapter 4.1 --- Introduction --- p.109 / Chapter 4.2 --- Materials & methods --- p.113 / Chapter 4.2.1 --- Sampling in the field --- p.113 / Chapter 4.2.2 --- Works in the laboratory --- p.114 / Chapter 4.3 --- Results --- p.116 / Chapter 4.3.1 --- Effects of algae on recruitment rates --- p.116 / Chapter 4.3.2 --- Effects of algae on colony mortality --- p.116 / Chapter 4.3.3 --- Effects of algae on absolute growth rates --- p.117 / Chapter 4.3.4 --- Effects of algae on the partial mortality frequency --- p.117 / Chapter 4.4 --- Discussion --- p.117 / Chapter Chapter 5 --- Summary and perspectives --- p.130 / References --- p.135

Woo Chi Kit. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2005. / Includes bibliographical references (leaves 275-287). / Abstracts in English and Chinese. / Acknowledgements --- p.i / Abstract --- p.ii / Contents --- p.vii / List of Tables --- p.xii / List of Figures --- p.xvi / Chapter Chapter 1: --- General Introduction / Chapter 1.1 --- Introduction --- p.1 / Chapter 1.1.1 --- Biotic disturbances --- p.1 / Chapter 1.1.1.1 --- Competition --- p.1 / Chapter 1.1.1.2 --- Bioerosion --- p.3 / Chapter 1.1.1.3 --- Predation --- p.4 / Chapter 1.1.1.4 --- Diseases --- p.6 / Chapter 1.1.2 --- Abiotic disturbances --- p.7 / Chapter 1.1.2.1 --- Fluctuating physical parameters --- p.7 / Chapter 1.1.2.2 --- Human activity --- p.8 / Chapter 1.1.2.3 --- Pollution --- p.9 / Chapter 1.1.2.4 --- Hurricanes --- p.10 / Chapter 1.1.2.5 --- Sedimentation --- p.11 / Chapter 1.1.3 --- Consequences of injuries --- p.11 / Chapter 1.1.3.1 --- Degradation of coral community --- p.12 / Chapter 1.1.3.2 --- Reduction of coral fitness --- p.14 / Chapter 1.1.3.3 --- Recovery from injuries --- p.15 / Chapter 1.2 --- Study Area --- p.17 / Chapter 1.3 --- Objectives --- p.18 / Chapter 1.4 --- Thesis outline --- p.19 / Chapter Chapter 2: --- The regeneration of artificial injuries on scleractinian corals / Chapter 2.1 --- Introduction --- p.22 / Chapter 2.2 --- Methods and Materials --- p.28 / Chapter 2.2.1 --- Study site --- p.28 / Chapter 2.2.2 --- Species chosen --- p.29 / Chapter 2.2.3 --- Tissue injury vs scraping injury --- p.29 / Chapter 2.2.4 --- Effect of colony size on lesion regeneration --- p.30 / Chapter 2.2.5 --- Seasonal differences in lesion regeneration --- p.31 / Chapter 2.2.6 --- Monitoring of injury recovery --- p.31 / Chapter 2.2.7 --- Tissue thickness of the coral species --- p.32 / Chapter 2.2.8 --- Water temperature --- p.32 / Chapter 2.2.9 --- Image and statistical analyses --- p.33 / Chapter 2.3 --- Results --- p.33 / Chapter 2.3.1 --- Regeneration pattern of artificial lesion --- p.34 / Chapter 2.3.1.1 --- Regeneration pattern of experiments in summer 2001 --- p.34 / Chapter 2.3.1.2 --- Regeneration pattern of experiments in autumn 2001 --- p.35 / Chapter 2.3.1.3 --- Regeneration pattern of experiments in winter 2001 --- p.36 / Chapter 2.3.1.4 --- Regeneration pattern of experiments in spring 2002 --- p.38 / Chapter 2.3.1.5 --- Regeneration pattern of experiments in summer 2002 --- p.39 / Chapter 2.3.1.6 --- Regeneration pattern of experiments in autumn 2002 --- p.39 / Chapter 2.3.2 --- Generalized recovery pattern --- p.41 / Chapter 2.3.3 --- Statistical analysis of the recovery time of the artificial lesion --- p.42 / Chapter 2.3.3.1 --- Colony size vs Recovery time --- p.43 / Chapter 2.3.3.2 --- Tissue injury vs Scraping injury --- p.43 / Chapter 2.3.3.3 --- Recovery times among species with artificial lesions --- p.44 / Chapter 2.3.3.4 --- Recovery time of artificial lesions inflicted at different seasons --- p.44 / Chapter 2.3.4 --- Photosynthetic activity of lesions inflicted by artificial injuries --- p.45 / Chapter 2.3.5 --- The tissue thickness of coral species --- p.48 / Chapter 2.3.6 --- Water temperature in Tung Ping Chau --- p.49 / Chapter 2.4 --- Discussion --- p.49 / Chapter 2.4.1 --- Rate of recovery in the artificial lesions --- p.49 / Chapter 2.4.2 --- Effects of colony size on the recovery of the artificial lesion --- p.51 / Chapter 2.4.3 --- Recovery of different injury types --- p.54 / Chapter 2.4.4 --- Interspecific differences on regeneration --- p.56 / Chapter 2.4.5 --- Seasonal differences in the recovery time of artificial lesions --- p.60 / Chapter 2.4.6 --- Photosynthetic activity of the artificial lesions --- p.62 / Chapter 2.4.7 --- Difficulties and and significance of the experiments --- p.65 / Chapter Chapter 3: --- The regeneration of selected coral species subjected to experimental breakage and toppling / Chapter 3.1 --- Introduction --- p.135 / Chapter 3.2 --- Methods and Materials --- p.139 / Chapter 3.2.1 --- Study site --- p.139 / Chapter 3.2.2 --- Species chosen --- p.140 / Chapter 3.2.3 --- Experimental breakage of Acropora digitifera --- p.140 / Chapter 3.2.4 --- Experimental toppling of selected coral species --- p.142 / Chapter 3.2.5 --- Image and statistical analysis --- p.143 / Chapter 3.3 --- Results --- p.143 / Chapter 3.3.1 --- The regeneration of Acropora digitifera colonies subjected to experimental breakage --- p.143 / Chapter 3.3.2 --- Photosynthetic activity of the fragments --- p.147 / Chapter 3.3.3 --- The regeneration of corals subjected to experimental toppling --- p.147 / Chapter 3.4 --- Discussion --- p.150 / Chapter 3.4.1 --- Rate of recovery of coral lesions inflicted by artificial breakage --- p.151 / Chapter 3.4.2 --- Size dependence of lesion recovery in artificial breakage study --- p.152 / Chapter 3.4.3 --- Fragmentation of the branching corals --- p.155 / Chapter 3.4.4 --- Recovery of experimental toppling --- p.159 / Chapter Chapter 4: --- The regeneration of bleached scleractinian corals / Chapter 4.1 --- Introduction --- p.185 / Chapter 4.2 --- Methods and Materials --- p.189 / Chapter 4.2.1 --- Study Site and Species chosen --- p.189 / Chapter 4.2.2 --- Recovery of bleached corals in summer 2001 --- p.190 / Chapter 4.2.3 --- Recovery of bleached corals in winter --- p.191 / Chapter 4.2.4 --- Physical parameters --- p.192 / Chapter 4.2.5 --- Statistical analysis --- p.192 / Chapter 4.3 --- Results --- p.193 / Chapter 4.3.1 --- Photosynthetic quantum yield of Hydnophora exesa --- p.193 / Chapter 4.3.2 --- Photosynthetic quantum yield of Montipora turgescens --- p.194 / Chapter 4.3.3 --- Photosynthetic quantum yield of winter bleached Pontes lutea --- p.195 / Chapter 4.3.4 --- Physical parameters --- p.197 / Chapter 4.4 --- Discussion --- p.199 / Chapter 4.4.1 --- Bleaching affects photosynthesis --- p.199 / Chapter 4.4.2 --- Temperature regulating the photosynthesis --- p.207 / Chapter 4.4.3 --- Consequence of coral bleaching --- p.209 / Chapter 4.4.4 --- Adaptive bleaching hypothesis --- p.210 / Chapter 4.4.5 --- Scope for corals in Hong Kong --- p.211 / Chapter Chapter 5: --- General health conditions of coral communities in Tung Ping Chau / Chapter 5.1 --- Introduction --- p.221 / Chapter 5.2 --- Methods and materials --- p.224 / Chapter 5.2.1 --- Study site --- p.224 / Chapter 5.2.2 --- Species chosen --- p.225 / Chapter 5.2.3 --- Belt transect and quadrat methods --- p.225 / Chapter 5.2.4 --- Definitions of injury types --- p.226 / Chapter 5.2.5 --- Statistical analysis --- p.229 / Chapter 5.3 --- Results --- p.229 / Chapter 5.3.1 --- General surveys of the corals --- p.229 / Chapter 5.3.2 --- Injuries on Platygyra acuta --- p.230 / Chapter 5.3.3 --- Injuries on Pontes lutea --- p.231 / Chapter 5.3.4 --- Injuries on Pavona decussata --- p.235 / Chapter 5.3.5 --- Statistical analysis --- p.236 / Chapter 5.4 --- Discussion --- p.237 / Chapter 5.4.1 --- Seasonal differences and the health of specific coral in Tung Ping Chau --- p.237 / Chapter 5.4.2 --- Partial mortality --- p.240 / Chapter 5.4.3 --- Recruitment of bivalves --- p.242 / Chapter 5.4.4 --- Physical damage on the coral surface --- p.243 / Chapter Chapter 6 --- Summary and Perspectives / Chapter 6.1 --- The regeneration of artificial injuries on scleractinian corals --- p.264 / Chapter 6.2 --- The regeneration of selected coral species subjected to experimental breakage and toppling --- p.267 / Chapter 6.3 --- The regeneration of injuries from natural impact on scleractinian coral --- p.269 / Chapter 6.4 --- General health conditions of selected coral species in Tung Ping Chau --- p.270 / Chapter 6.5 --- Significance of the findings of the experiments carried out in this study --- p.271 / Chapter 6.6 --- Limitations and future works --- p.273 / References --- p.275

石珊瑚是具有自營及異營功能的生物，近年來，異營功能被認為是石珊瑚很重要的營養來源，可令牠們從珊瑚白化中復原。香港每年的海水溫度可由冬天的攝氏十三度升到夏天的三十度，這季節性的溫度變異令香港成為石珊瑚生存的邊緣地方，石珊瑚只能組成群落但不能成礁。雖然環境因素對於石珊瑚的生長並不理想，但大型的珊瑚白化仍沒有發生，這意味著香港的珊瑚比較能夠適應香港的嚴峻困難環境，珊瑚具有的異營功能或許能夠提供牠們額外的能量，作為日常新陳代謝之用。所以，這研究的目標是找出異營功能對香港石珊瑚的重要性，這研究以豐年蝦的無節幼體(Artemia salina nauplii)及團塊角孔珊瑚(Goniopora lobata)作為實驗對象，以找出石珊瑚怎樣應用異營功能來加快生長、提高生理反應及增加能量儲備。此外，這研究還成立了一種量化珊瑚白化的方法，以提供一種簡單、快捷、客觀及不破壞珊瑚為前提的方法來監測珊瑚的健康。 / 本研究紀錄了七種香港常見但具有不同珊瑚蟲大小的石珊瑚的攝食速率，結果發現團塊角孔珊瑚的攝食速率最高，每小時每公升每平方厘米珊瑚表面積的攝食率在白天和晚上分別為203±90隻及145±79隻豐年蝦的無節幼體。攝食速率跟珊瑚蟲面積大小及豐年蝦的密度有著正面的相互關係。團塊角孔珊瑚與其它石珊瑚在外觀上有所不同，牠們無論白天或是晚上也會伸出自己的觸手，這特色令牠們可以攝取更多食物，所以牠們被選為這次研究的實驗珊瑚品種。 / 在異營的情況下，團塊角孔珊瑚的蟲黃藻密度及葉綠素a的濃度在一個月後倍增，由每平方厘米珊瑚表面積的2.75±0.50 x 10⁶蟲黃藻及每平方厘米珊瑚表面積每毫升的23.82±5.42微克葉綠素a到6.00±1.57 x 10⁶蟲黃藻及每平方厘米珊瑚表面積每毫升的53.56±17.66微克葉綠素a，但沒有異營的珊瑚則沒有任何轉變。`此外，從實驗的第二個星期起，應用異營功能的情況下珊瑚的鈣化速率會較快，平均達到每平方厘米珊瑚表面積每小時每公升100微克的生長。無論有異營與否，珊瑚的最大光合作用量子效率也保持在0.6左右。 / 本研究在數碼照片及電腦圖像分析軟件的幫助下，成立了量化珊瑚白化一種簡單、客觀、無破壞性及便宜的方法。這方法使用一塊貼上黑色及白色膠紙的金屬架作為黑白色的參考，再以數碼照片去量度白化的百分比，這方法測出白化了的濱珊瑚屬個體可以達到100%的白化百分比，此外，白化百分比與光合作用效率及蟲黃藻的密度有反向的關係。這方法能有效地在水底定期監測珊瑚的顏色變化，實驗的結果顯示團塊角孔珊瑚的顏色在一年間能有顯著的變化，在春天及秋天牠們只有少於20%的白化百分比，但在夏天及冬天則有超過30%的白化百分比，這跟光合作用效率有反向的關係。 / 在季節性溫度模擬實驗中反映出異營功能可以幫助珊瑚保持光合作用效率及帶來一個較和緩的珊瑚顏色轉變，此外，從團塊角孔珊瑚珊瑚蟲/觸手的長度得知，異營功能能夠令牠們的珊瑚蟲/觸手伸得更長，反映出利用異營功能的珊瑚個體比較健康及能主動地攝取食物。 / 在一天攝氏一度的溫度轉變的另一個實驗下，團塊角孔珊瑚的白化百分比隨著溫度轉變而增加，由20%增至60%，此外，長期的高溫壓力對於牠們較有破壞性，實驗結果顯示團塊角孔珊瑚在攝氏三十四度的高溫下會把其珊瑚蟲及觸手縮回在骨骼裏，而其白化百分比在實驗後的兩個月仍沒有下降的現象；珊瑚在攝氏十二度的低溫壓力下，並慢慢地回復到牠們合適的水溫後，牠們的顏色則漸變正常，珊瑚蟲/觸手也慢慢伸出來。但在更低的低溫壓力下(攝氏十度)，珊瑚蟲則從骨骼裏脫離，不能再回復。珊瑚蟲/觸手的長度或許能夠顯示珊瑚的健康及攝食狀態，實驗結果顯示珊瑚蟲/觸手的長度與水溫一起上升，但在低溫及攝氏三十度下，珊瑚蟲/觸手會慢慢縮回。利用異營功能與否對牠們的熱適應沒有任何分別，在攝氏十二度的低溫情況下，異營更帶來負面的影響，致珊瑚有較短的半致死時間。所以，在極端低溫及高溫的情況下，石珊瑚可能使用了很多的能量去抵抗轉變，但確不能從異營中取得額外的營養。本研究最後一個實驗正正反映出這個實況，展示出團塊角孔珊瑚最佳的攝食溫度為攝氏二十三度，每小時每公升每珊瑚蟲可進食28.11±4.59隻豐年蝦，但在攝氏十四跟三十二度下，牠們每小時每公升每珊瑚蟲只吃了約6隻豐年蝦。異營功能在合適的溫度下能夠提高珊瑚的能量儲備及蟲黃藻的密度，但在極端的溫度下，能量儲備則減少，甚至比自營的珊瑚個體還要低。總括而言，異營及自營功能對石珊瑚都是非常重要，但異營功能並不是絶對可以幫助珊瑚去抵抗嚴峻的環境壓力。 / 這次研究幫助認識了異營功能對香港珊瑚群落的作用，從而知道它能夠提供營養，提高蟲黃藻密度及能量儲備，香港石珊瑚可能依靠異營功能來適應香港特殊的環境。 / Scleractinian corals form coral communities in Hong Kong, a marginal area for their growth because of its fluctuating seawater surface temperature (SST) that ranged from 13 to 30ºC throughout a year. In spite of this, mass coral bleaching has not occurred in Hong Kong. It may be possible that Hong Kong corals are tougher, well adapted to the Hong Kong stressful environment. Heterotrophy may contribute significantly to their daily metabolic demand. This research therefore aimed at finding out the roles of heterotrophy in Hong Kong corals using Artemia salina nauplii as their food. / Goniopora lobata exhibited the highest feeding rate among all species tested. It is unique in having its polyps and tentacles extended all day long. This characteristic allows it to grab more food during the day than the other coral species examined and hence it was chosen to be the candidate for heterotrophy studies in this research. / With heterotrophy (Artemia salina nauplii feeding), zooxanthellae density and Chl a concentration were doubled in fed G. lobata colonies in 4 weeks. Calcification rates of fed colonies were generally higher than those of unfed colonies starting from the second week of a four week experiment. / Using digital imagery and computer image analysis, an easy, objective, non-destructive and inexpensive method was developed to quantify coral bleaching in terms of its % whiteness. This % whiteness of a coral is expressed with reference to the black and white markers around a metal frame or PVC plates. It was negatively correlated with photosynthetic efficiency and zooxanthellae density. When applied on G. lobata in situ, it was found that this coral showed seasonal fluctuation with < 20% whiteness in spring and autumn, but greater than 30% whiteness in summer and winter. / Experimental set up with seasonal temperature fluctuation pattern simulating that in the field revealed that heterotrophy can help to sustain photosynthetic yield and elicit a gentle coral colour change in G. lobata over time. Moreover, fed G. lobata extended their polyps / tentacles at a greater length than the unfed colonies, suggesting that fed colonies were more healthy and active in capturing food. / Heat stress was found to be more deleterious to G. lobata colonies such that they cannot extend their polyp / tentacles nor regain their colour two months after the thermal tolerance experiment using Chronic Lethal Methodologies (CLM) approach. In contrast, colonies of G. lobata cold-stressed at 12ºC had their colour returned to normal and their polyps / tentacles extended after a few days. The degree of extension of polyp / tentacle of G. lobata could thus be used as an indication of its health or feeding status. Under the cold stressed treatment of 12ºC, heterotrophy was even detrimental and a lower median lethal time (LT50) was found in fed colonies. Hence, it is likely that corals under extreme low and high temperatures would deplete more of their energy reserves and could not replenish them because of decline in their feeding rates. To verify this, additional experiment was carried out to evaluate the relationship between coral feeding rates, symbiont responses and energy reserves at a wide range of temperature from 14ºC to 32ºC. Results showed that feeding rate of G. lobata was optimal at 23ºC and much lowered at extremes. It also showed that heterotrophy was important in enhancing coral energy reserves and symbiont density under optimal feeding temperatures (23ºC and 27.5ºC) but less important under extreme temperatures such that energy reserves became even lower than that in the unfed colonies. This suggests that heterotrophy and autotrophy are both important to coral nutrition. Under optimal condition, heterotrophy could play a significant role in supplementing corals with additional energy reserves that could be used to overcome stresses. However, under extreme conditions, feeding stops and heterotrophy can no longer play its role and at times, could even be detrimental to the survival of the corals. / These findings from all the experiments are useful in providing the insight needed to understand the role of heterotrophy in Hong Kong corals and their effects on various physiological responses. Heterotrophy is important to provide nutrients for better growth, higher symbiont density and increased energy reserves and it may be the reasons why Hong Kong corals are tougher and can withstand a wide range of temperature fluctuation throughout a year. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Chow, Ming Him. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2012. / Includes bibliographical references (leaves 221-251). / Abstracts also in Chinese. / Acknowledgements --- p.i / Abstract --- p.ii / 摘要 --- p.vi / Contents --- p.viii / List of Tables --- p.xv / List of Figures --- p.xvi / Chapter Chapter 1 --- General Introduction / Chapter 1.1 --- Introduction --- p.1 / Chapter 1.1.1 --- Coral reef and its importance --- p.1 / Chapter 1.1.2 --- Scleractinian corals and coral-algal symbiosis --- p.3 / Chapter 1.1.3 --- Heterotrophic nutrition --- p.4 / Chapter 1.1.4 --- Autotrophy-heterotrophy dynamics --- p.6 / Chapter 1.1.5 --- Coral growth and calcification under heterotrophy --- p.7 / Chapter 1.1.6 --- Environmental stressors and coral bleaching --- p.9 / Chapter 1.1.7 --- Coral status in Hong Kong --- p.11 / Chapter 1.2 --- Significance of the project --- p.14 / Chapter 1.3 --- Study objectives --- p.15 / Chapter 1.4 --- Study site Wu Pai (Crescent Island) and Chek Chau (Port Island) --- p.16 / Chapter 1.5 --- Coral species chosen for the experiments --- p.17 / Chapter 1.6 --- Thesis outline --- p.18 / Chapter Chapter 2 --- Diurnal Heterotrophy in Corals as a Function of Their Polyp Size / Chapter 2.1 --- Introduction --- p.23 / Chapter 2.2 --- Materials and Methods --- p.26 / Chapter 2.2.1 --- Site description and sample collection --- p.26 / Chapter 2.2.2 --- Feeding experiments --- p.27 / Chapter 2.2.3 --- Artemia density count and feeding rate determination --- p.28 / Chapter 2.2.4 --- Data analysis --- p.29 / Chapter 2.3 --- Results --- p.30 / Chapter 2.3.1 --- Feeding rate of scleractinian corals between day and night --- p.30 / Chapter 2.3.2 --- Relationships between feeding rate and coral polyp area --- p.31 / Chapter 2.3.3 --- Relationship between feeding rate, Artemia concentration and feeding duration --- p.32 / Chapter 2.4 --- Discussion --- p.34 / Chapter 2.4.1 --- Feeding rate of scleractinian corals --- p.34 / Chapter 2.4.2 --- Hong Kong underwater environment --- p.38 / Chapter 2.4.3 --- Goniopora lobata as an active feeder --- p.39 / Chapter 2.4.4 --- Day and night differences --- p.40 / Chapter 2.4.5 --- Mechanisms of coral heterotrophy --- p.42 / Chapter 2.5 --- Summary --- p.43 / Chapter Chapter 3 --- Effects of Heterotrophy on the Growth and Photosynthetic Physiological Responses of Goniopora lobata / Chapter 3.1 --- Introduction --- p.52 / Chapter 3.2 --- Materials and Methods --- p.55 / Chapter 3.2.1 --- Sample collection and conditioning --- p.55 / Chapter 3.2.2 --- Coral culture experiment --- p.56 / Chapter 3.2.3 --- Feeding rate determination 57 / Chapter 3.2.4 --- Measurements of zooxanthellae density and chlorophyll a concentration --- p.57 / Chapter 3.2.5 --- Measurements of calcification rate --- p.59 / Chapter 3.2.6 --- Measurements of photosynthetic efficiency of corals --- p.61 / Chapter 3.2.7 --- Data analysis --- p.61 / Chapter 3.3 --- Results --- p.62 / Chapter 3.3.1 --- Feeding rate --- p.62 / Chapter 3.3.2 --- Zooxanthellae density and chlorophyll a concentration --- p.63 / Chapter 3.3.3 --- Calcification rate --- p.63 / Chapter 3.3.4 --- Maximum quantum yield --- p.64 / Chapter 3.4 --- Discussion --- p.65 / Chapter 3.4.1 --- Coral feeding rate, zooxanthellae density and chlorophyll a concentration --- p.65 / Chapter 3.4.2 --- Calcification rate --- p.67 / Chapter 3.4.3 --- Photosynthetic responses in fed and unfed corals --- p.69 / Chapter 3.5 --- Summary --- p.70 / Chapter Chapter 4 --- Quantifying the Degree of Coral Bleaching using Photoquadrat and Computer Image Analysis / Chapter 4.1 --- Introduction --- p.76 / Chapter 4.2 --- Materials and Methods --- p.79 / Chapter 4.2.1 --- Design of photoquadrat --- p.79 / Chapter 4.2.2 --- Photo image analysis --- p.80 / Chapter 4.2.3 --- Trial run and normalization of the technique --- p.81 / Chapter 4.2.3.1 --- Intensity of normal and bleached sections of a coral Porites sp. --- p.81 / Chapter 4.2.3.2 --- Intensity of coral Goniopora lobata under different exposure settings and contrasts --- p.82 / Chapter 4.2.4 --- Field application of the technique on other coral species --- p.82 / Chapter 4.2.5 --- Evaluation of the use of % whiteness to estimate photosynthetic physiological states of the coral Goniopora lobata --- p.83 / Chapter 4.2.5.1 --- Collection and photo taking of samples --- p.83 / Chapter 4.2.5.2 --- Photosynthetic quantum yield --- p.84 / Chapter 4.2.5.3 --- Tissue extraction and sample preservation for zooxanthellae and chlorophyll a measurements --- p.84 / Chapter 4.2.5.4 --- Zooxanthellae density count and determination of chlorophyll a concentration --- p.85 / Chapter 4.2.6 --- Data analysis --- p.86 / Chapter 4.3 --- Results --- p.87 / Chapter 4.3.1 --- Percent whiteness calculation --- p.87 / Chapter 4.3.2 --- Normalization of the technique --- p.88 / Chapter 4.3.2.1 --- Effect of simulated changes in light condition (exposure compensation) on % whiteness estimation --- p.88 / Chapter 4.3.2.2 --- Effect of simulated changes in turbidity (contrasts) on % whiteness estimation --- p.88 / Chapter 4.3.3 --- Colour change in common coral species at different seasons --- p.89 / Chapter 4.3.4 --- Relationship between % whiteness and photosynthetic physiological states of corals --- p.89 / Chapter 4.3.4.1 --- Effective quantum yield vs % whiteness --- p.90 / Chapter 4.3.4.2 --- Zooxanthellae density per coral surface area vs % whiteness --- p.90 / Chapter 4.3.4.2 --- Chlorophyll a concentration per cm² coral surface area vs % whiteness --- p.91 / Chapter 4.4 --- Discussion --- p.91 / Chapter 4.4.1 --- Measure of coral colour in terms of % whiteness --- p.92 / Chapter 4.4.2 --- Effects of extreme conditions in estimating coral % whiteness --- p.93 / Chapter 4.4.3 --- Changes in intensity of coral colours at different seasons --- p.95 / Chapter 4.4.4 --- Comparison with other approaches to quantify coral colour change --- p.96 / Chapter 4.4.5 --- Estimation of coral % whiteness as a tool to assess photosynthetic physiological state of corals --- p.98 / Chapter 4.4.6 --- Potential limitations of the technique --- p.100 / Chapter 4.5 --- Summary --- p.101 / Chapter Chapter 5 --- High and Low Thermal Tolerance Limits of Goniopora lobata / Chapter 5.1 --- Introduction --- p.112 / Chapter 5.2 --- Materials and Methods --- p.116 / Chapter 5.2.1 --- Sample collection and conditioning --- p.116 / Chapter 5.2.2 --- Polyp / tentacle length classification of Goniopora lobata --- p.117 / Chapter 5.2.3 --- Upper thermal limit experiment (Experiment 1) --- p.118 / Chapter 5.2.4 --- Lower thermal limit experiment (Experiments 2A and 2B) --- p.118 / Chapter 5.2.5 --- Data analysis --- p.119 / Chapter 5.3 --- Results --- p.120 / Chapter 5.3.1 --- Experiment 1 (Upper thermal tolerances of corals) --- p.120 / Chapter 5.3.1.1 --- Daily changes in the frequency of polyp / tentacle length classes of coral colonies --- p.120 / Chapter 5.3.1.2 --- Mortality and LT₅₀ --- p.121 / Chapter 5.3.1.3 --- % whiteness --- p.121 / Chapter 5.3.2 --- Experiment 2A (Lower thermal tolerances of corals, lower limit: 12ºC) --- p.122 / Chapter 5.3.2.1 --- Daily changes in the frequency of polyp / tentacle length classes of coral colonies --- p.122 / Chapter 5.3.2.2 --- Mortality and LT₅₀ --- p.123 / Chapter 5.3.2.3 --- % whiteness --- p.123 / Chapter 5.3.3 --- Experiment 2B (Lower thermal tolerances of corals, lower limit: 10ºC) --- p.124 / Chapter 5.3.3.1 --- Daily changes in the frequency of polyp / tentacle length classes of coral colonies --- p.124 / Chapter 5.3.3.2 --- Mortality and LT₅₀ --- p.125 / Chapter 5.3.3.3 --- % whiteness --- p.125 / Chapter 5.4 --- Discussion --- p.126 / Chapter 5.4.1 --- Polyp / tentacle lengths of Goniopora lobata under different temperatures --- p.126 / Chapter 5.4.2 --- The effects of heterotrophy (feeding) on G. lobata survivorship under extreme temperatures --- p.127 / Chapter 5.4.3 --- Coral colour and bleaching --- p.128 / Chapter 5.4.4 --- Upper, lower thermal tolerances and LT₅₀ of Goniopora lobata --- p.128 / Chapter 5.4.5 --- Coral recovery --- p.129 / Chapter 5.4.6 --- Corals after thermal stress --- p.130 / Chapter 5.4.7 --- Application of CLM approach and its implications --- p.131 / Chapter 5.5 --- Summary --- p.132 / Chapter Chapter 6 --- Seasonal Variations in Coral Colour and Physiological Responses of Goniopora lobata in situ and ex situ / Chapter 6.1 --- Introduction --- p.142 / Chapter 6.2 --- Materials and Methods --- p.147 / Chapter 6.2.1 --- Seasonal field study --- p.147 / Chapter 6.2.2 --- Laboratory study --- p.148 / Chapter 6.2.3 --- Data analysis --- p.150 / Chapter 6.3 --- Results --- p.152 / Chapter 6.3.1 --- Ambient seawater temperature, effective quantum yield and % whiteness of Goniopora lobata colonies in the natural environment --- p.152 / Chapter 6.3.2 --- Zooplankton abundance and biomass --- p.153 / Chapter 6.3.3 --- Responses of G. lobata under the simulated environmental conditions --- p.154 / Chapter 6.3.3.1 --- Coral mortality --- p.154 / Chapter 6.3.3.2 --- Seasonal maximum quantum yields --- p.155 / Chapter 6.3.3.3 --- Seasonal feeding rates --- p.155 / Chapter 6.3.3.4 --- Seasonal change in coral colours --- p.156 / Chapter 6.4 --- Discussion --- p.156 / Chapter 6.4.1 --- Coral colour change, effective quantum yield, seawater temperature, zooplankton abundance and coral heterotrophy in the natural environment --- p.157 / Chapter 6.4.2 --- Coral responses under simulated seasonal change conditions --- p.160 / Chapter 6.4.3 --- Comparison of coral responses to seasonal change under natural and simulated laboratory conditions --- p.163 / Chapter 6.4.4 --- Limitations of this simulation approach --- p.165 / Chapter 6.5 --- Summary --- p.167 / Chapter Chapter 7 --- Effects of Temperature and Heterotrophy on Physiological Responses and Energy Reserves of Goniopora lobata / Chapter 7.1 --- Introduction --- p.177 / Chapter 7.2 --- Materials and Methods --- p.180 / Chapter 7.2.1 --- Sample collection and acclimation --- p.180 / Chapter 7.2.2 --- Design of the experiment --- p.181 / Chapter 7.2.3 --- Artemia feeding experiments --- p.181 / Chapter 7.2.4 --- Coral tissue extraction and analysis --- p.182 / Chapter 7.2.4.1 --- Zooxanthellae and chlorophyll a measurement --- p.183 / Chapter 7.2.4.2 --- Protein content analysis --- p.184 / Chapter 7.2.4.3 --- Carbohydrate content analysis --- p.184 / Chapter 7.2.4.4 --- Total lipid content analysis --- p.185 / Chapter 7.2.5 --- Photosynthetic quantum yield measurement --- p.186 / Chapter 7.2.6 --- Coral colour quantification --- p.186 / Chapter 7.2.7 --- Data analysis --- p.187 / Chapter 7.3 --- Results --- p.188 / Chapter 7.3.1 --- Feeding rate --- p.188 / Chapter 7.3.2 --- Zooxanthellae density --- p.188 / Chapter 7.3.3 --- Chlorophyll a (Chl a) content --- p.190 / Chapter 7.3.4 --- Protein content --- p.191 / Chapter 7.3.5 --- Carbohydrate contents --- p.191 / Chapter 7.3.6 --- Total lipids --- p.192 / Chapter 7.3.7 --- Maximum quantum yield --- p.193 / Chapter 7.3.8 --- Coral colour --- p.194 / Chapter 7.4 --- Discussion --- p.195 / Chapter 7.4.1 --- Feeding responses under different temperatures --- p.196 / Chapter 7.4.2 --- Symbiont responses under different temperatures --- p.198 / Chapter 7.4.3 --- Energy reserves --- p.199 / Chapter 7.4.4 --- Autotrophy-heterotrophy dynamics --- p.201 / Chapter 7.5 --- Summary --- p.202 / Chapter Chapter 8 --- Summary and Perspectives --- p.212 / References --- p.221

Chui, Pui Yi. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2011. / Includes bibliographical references (leaves 133-149). / Abstracts in English and Chinese. / Abstract (English) --- p.i / Abstract (Chinese) --- p.v / Acknowledgements --- p.vii / Contents --- p.viii / List of Tables --- p.xi / List of Figures --- p.xii / Chapter Chapter 1 --- General Introduction and Thesis Outline --- p.1 / Chapter 1.1 --- Introduction --- p.1 / Chapter 1.1.1 --- Coral reefs and conservation --- p.1 / Chapter 1.1.2 --- Reproduction in scleractinian corals --- p.3 / Chapter 1.1.2.1 --- Sexual reproductive pattern --- p.3 / Chapter 1.1.2.2 --- Overview of coral spawning patterns --- p.5 / Chapter 1.1.2.3 --- Environmental factors regulating coral reproduction --- p.7 / Chapter 1.1.3 --- Coral recruitment --- p.9 / Chapter 1.2 --- Coral Communities in Hong Kong --- p.12 / Chapter 1.3 --- Objectives --- p.13 / Chapter 1.4 --- Study Sites- Tung Ping Chau Marine Park --- p.14 / Chapter 1.5 --- Thesis outline --- p.15 / Chapter Chapter 2 --- "Spawning of Scleractinian Corals in Hong Kong, Larval Culture and Development" --- p.20 / Chapter 2.1 --- Introduction --- p.20 / Chapter 2.2 --- Methods and Materials --- p.22 / Chapter 2.2.1 --- Site description --- p.22 / Chapter 2.2.2 --- Spawning observation --- p.23 / Chapter 2.2.3 --- "Target coral species, Platygyra acuta" --- p.23 / Chapter 2.2.4 --- Coral gamete collection --- p.24 / Chapter 2.2.5 --- Fertilization and larval rearing --- p.26 / Chapter 2.2.6 --- Embryonic development of Platygyra acuta larvae --- p.28 / Chapter 2.2.7 --- Induced settlement of coral larvae --- p.29 / Chapter 2.2.8 --- Environmental cues that triggered the spawning events --- p.30 / Chapter 2.3 --- Results --- p.31 / Chapter 2.3.1 --- Spawning observation --- p.31 / Chapter 2.3.1.1 --- May 2009 --- p.32 / Chapter 2.3.1.2 --- May- Early June 2010 --- p.33 / Chapter 2.3.1.3 --- Late June 2010 --- p.36 / Chapter 2.3.1.4 --- July 2010 --- p.38 / Chapter 2.3.2 --- Fertilization and Platygyra acuta larval rearing --- p.38 / Chapter 2.3.3 --- Embryonic development of Platygyra acuta larvae --- p.39 / Chapter 2.3.4 --- Induced settlement --- p.40 / Chapter 2.4 --- Discussion --- p.40 / Chapter 2.4.1 --- Spawning observation --- p.40 / Chapter 2.4.2 --- Embryonic development of Platygyra acuta --- p.43 / Chapter 2.4.3 --- Environmental cues --- p.44 / Chapter 2.4.4 --- "Fertilization, larval rearing and induced settlement" --- p.46 / Chapter 2.5 --- Summary --- p.46 / Chapter Chapter 3 --- "Recruitment Patterns of Scleractinian Corals in Tung Ping Chau Marine Park, Hong Kong" --- p.70 / Chapter 3.1 --- Introduction --- p.70 / Chapter 3.2 --- Methods and Materials --- p.74 / Chapter 3.2.1 --- Site description --- p.74 / Chapter 3.2.2 --- Settlement and survival of coral recruits --- p.74 / Chapter 3.2.2.1 --- Settlement tiles --- p.74 / Chapter 3.2.2.2 --- Concrete blocks --- p.77 / Chapter 3.2.2.3 --- Fouling organisms on settlement tiles --- p.77 / Chapter 3.2.3 --- Environmental parameters --- p.78 / Chapter 3.2.4 --- Post-settlement survival of artificially seeded coral recruits of Platygyra acuta --- p.78 / Chapter 3.2.5 --- Effect of gastropod exclusion on post-settlement survival of coral recruits --- p.79 / Chapter 3.2.6 --- Data analysis --- p.81 / Chapter 3.3 --- Results --- p.82 / Chapter 3.3.1 --- Coral recruitment on settlement tiles --- p.82 / Chapter 3.3.1.1 --- Total settlement --- p.82 / Chapter 3.3.1.2 --- Spatial and temporal patterns of coral recruitment --- p.83 / Chapter 3.3.1.3 --- Growth and health of coral recruit --- p.84 / Chapter 3.3.1.4 --- Competition with other fouling organisms --- p.85 / Chapter 3.3.2 --- Coral recruitment on concrete blocks --- p.88 / Chapter 3.3.3 --- Environmental parameters --- p.89 / Chapter 3.3.4 --- Post-settlement survival of artificially seeded coral recruits of Platygyra acuta --- p.91 / Chapter 3.3.5 --- Effects of gastropod of exclusion on post-settlement survival of coral recruits --- p.92 / Chapter 3.4 --- Discussion --- p.93 / Chapter 3.4.1 --- Coral settlement --- p.93 / Chapter 3.4.1.1 --- Low settlement rate of corals --- p.94 / Chapter 3.4.1.2 --- Possible cause of low coral settlement --- p.96 / Chapter 3.4.2 --- Post-settlement survival of coral recruits --- p.100 / Chapter 3.4.2.1 --- Effect of high sedimentation rate --- p.100 / Chapter 3.4.2.2 --- Competition and predation by other marine organisms --- p.101 / Chapter 3.5 --- Summary --- p.104 / Chapter Chapter 4 --- Summary and Perspectives --- p.126 / References --- p.133

Hui, Yuk Ling. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2010. / Includes bibliographical references (leaves 132-146). / Abstracts in English and Chinese. / Acknowledgements --- p.i / Abstract (English) --- p.ii / Abstract (Chinese) --- p.vi / Contents --- p.viii / List of Tables --- p.xi / List of Figures --- p.xiii / Chapter Chapter 1 --- Introduction --- p.1 / Chapter 1.1 --- General biology of scleractinian corals --- p.1 / Chapter 1.2 --- Global coral degradation --- p.2 / Chapter 1.3 --- Effects of temperature and other environmental factors on coral growth and development --- p.4 / Chapter 1.4 --- Restoration strategies --- p.6 / Chapter 1.5 --- Scleractinian corals in Hong Kong and study site of this thesis research --- p.9 / Chapter 1.6 --- Target coral species --- p.10 / Chapter 1.7 --- Objectives --- p.11 / Chapter 1.8 --- Thesis outline --- p.12 / Chapter Chapter 2 --- "Gametogenic Cycles of Acropora tumida in Cheung Sha Wan,Tung Ping Chau, HKSAR" --- p.17 / Chapter 2.1 --- Introduction --- p.17 / Chapter 2.2 --- Methods and Materials --- p.20 / Chapter 2.2.1 --- Samples collection --- p.20 / Chapter 2.2.2 --- Histology --- p.20 / Chapter 2.2.3 --- Gamete classification and measurements --- p.21 / Chapter 2.2.4 --- Temperature records --- p.23 / Chapter 2.2.5 --- Data analysis --- p.23 / Chapter 2.3 --- Results --- p.23 / Chapter 2.3.1 --- Gametogenic cycle of Acropora tumida --- p.23 / Chapter 2.3.2 --- Oogenesis in Acropora tumida --- p.24 / Chapter 2.3.3 --- Spermatogenesis in Acropora tumida --- p.29 / Chapter 2.3.4 --- Temperature data --- p.30 / Chapter 2.4 --- Discussion --- p.31 / Chapter 2.4.1 --- Gametogenic cycle of Acropora tumida --- p.31 / Chapter 2.4.2 --- Oogenesis in Acropora tumida --- p.32 / Chapter 2.4.3 --- Spermatogenesis in Acropora tumida --- p.34 / Chapter Chapter 3 --- Comparison on the Oogenesis in Acropora tumida Grown Ex situ and In situ --- p.44 / Chapter 3.1 --- Introduction --- p.44 / Chapter 3.2 --- Methods and Materials --- p.48 / Chapter 3.2.1 --- Samples collection --- p.48 / Chapter 3.2.2 --- Histological analysis --- p.50 / Chapter 3.2.3 --- Environmental conditions --- p.50 / Chapter 3.2.4 --- Data analysis --- p.51 / Chapter 3.3 --- Results --- p.52 / Chapter 3.3.1 --- Comparison of oogenesis in ex situ and in situ Acropora tumida samples --- p.52 / Chapter 3.3.2 --- Comparison of spermary development in ex situ and in situ Acropora tumida samples --- p.54 / Chapter 3.3.3 --- Environmental conditions --- p.54 / Chapter 3.4 --- Discussion --- p.55 / Chapter Chapter 4 --- Oogenesis along a Fragmentation Gradient in the Branching coral Acropora tumida --- p.70 / Chapter 4.1 --- Introduction --- p.70 / Chapter 4.2 --- Methods and Materials --- p.74 / Chapter 4.2.1 --- Samples collection and histological analysis --- p.74 / Chapter 4.2.2 --- Data analysis --- p.76 / Chapter 4.3 --- Results --- p.76 / Chapter 4.3.1 --- Oogenesis in intact Acropora tumida colonies --- p.76 / Chapter 4.3.2 --- Oogenesis in Acropora tumida fragments --- p.77 / Chapter 4.3.3 --- Sterile zone in Acropora tumida branch tips --- p.78 / Chapter 4.4 --- Discussion --- p.79 / Chapter Chapter 5 --- "Temperature Effects on the Survivorship, Growth and Oogenesis in Acropora tumida Fragments Grown under Laboratory Conditions " --- p.87 / Chapter 5.1 --- Introduction --- p.87 / Chapter 5.2 --- Methods and Materials --- p.91 / Chapter 5.2.1 --- Samples collection --- p.91 / Chapter 5.2.2 --- Samples culture --- p.92 / Chapter 5.2.3 --- Survivorship --- p.93 / Chapter 5.2.4 --- Growth measurement --- p.94 / Chapter 5.2.5 --- Reproductive analysis --- p.94 / Chapter 5.2.6 --- Statistical analysis --- p.95 / Chapter 5.3 --- Results --- p.95 / Chapter 5.3.1 --- Temperatures in ex situ ambient aquaria and the in situ site at Tung Ping Chau --- p.95 / Chapter 5.3.2 --- Survivorship of coral branches --- p.96 / Chapter 5.3.3 --- Growth measurement --- p.97 / Chapter 5.3.4 --- Oogenic development --- p.98 / Chapter 5.3.4.1 --- Oocyte developmental stages --- p.99 / Chapter 5.3.4.2 --- Oocyte size measurement --- p.100 / Chapter 5.3.4.3 --- Oocyte density --- p.103 / Chapter 5.3.5 --- Spermary developmental stages --- p.105 / Chapter 5.4 --- Discussion --- p.105 / Chapter 5.4.1 --- Survivorship --- p.105 / Chapter 5.4.2 --- Growth measurement --- p.107 / Chapter 5.4.3 --- Oogenesis under different temperature conditions --- p.109 / Chapter 5.4.3.1 --- Oocyte developmental stage --- p.109 / Chapter 5.4.3.2 --- Oocyte size measurement and density --- p.113 / Chapter 5.4.5 --- Spermary developmental stage --- p.114 / Chapter Chapter 6 --- Summary and Perspectives --- p.128 / References --- p.132